[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

MA49566A - Carboxamides utilisés en tant qu'inhibiteurs des canaux sodiques - Google Patents

Carboxamides utilisés en tant qu'inhibiteurs des canaux sodiques

Info

Publication number
MA49566A
MA49566A MA049566A MA49566A MA49566A MA 49566 A MA49566 A MA 49566A MA 049566 A MA049566 A MA 049566A MA 49566 A MA49566 A MA 49566A MA 49566 A MA49566 A MA 49566A
Authority
MA
Morocco
Prior art keywords
sodium channel
channel inhibitors
carboxamides used
carboxamides
inhibitors
Prior art date
Application number
MA049566A
Other languages
English (en)
Inventor
Nadia Ahmad
Corey Anderson
Vijayalaksmi Arumugam
Iuliana Luci Asgian
Joanne Louise Camp
Lev Tyler Dewey Fanning
Ruah Sara Sabina Hadida
Dennis Hurley
Lidio Marx Carvalho Meireles
Urvi Patel
Yvonne Schmidt
David Shaw
Stephen Andrew Thomson
Original Assignee
Vertex Pharma
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Vertex Pharma filed Critical Vertex Pharma
Publication of MA49566A publication Critical patent/MA49566A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/54Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/58Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/64Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/69Two or more oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • C07D213/82Amides; Imides in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/34One oxygen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/86Benzo [b] furans; Hydrogenated benzo [b] furans with an oxygen atom directly attached in position 7
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Rheumatology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Furan Compounds (AREA)
  • Pyridine Compounds (AREA)
MA049566A 2017-07-11 2018-07-11 Carboxamides utilisés en tant qu'inhibiteurs des canaux sodiques MA49566A (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762531313P 2017-07-11 2017-07-11
US201762608283P 2017-12-20 2017-12-20

Publications (1)

Publication Number Publication Date
MA49566A true MA49566A (fr) 2020-05-20

Family

ID=63036498

Family Applications (1)

Application Number Title Priority Date Filing Date
MA049566A MA49566A (fr) 2017-07-11 2018-07-11 Carboxamides utilisés en tant qu'inhibiteurs des canaux sodiques

Country Status (23)

Country Link
US (3) US10647661B2 (fr)
EP (1) EP3651752A1 (fr)
JP (1) JP7277431B2 (fr)
KR (1) KR20200026987A (fr)
CN (1) CN111065383A (fr)
AU (1) AU2018300150A1 (fr)
BR (1) BR112020000553A2 (fr)
CA (1) CA3069720A1 (fr)
CL (1) CL2020000075A1 (fr)
CO (1) CO2020000145A2 (fr)
CR (1) CR20200064A (fr)
DO (1) DOP2020000004A (fr)
EC (1) ECSP20003147A (fr)
IL (1) IL271948A (fr)
JO (1) JOP20200001A1 (fr)
MA (1) MA49566A (fr)
PE (1) PE20201164A1 (fr)
PH (1) PH12020500066A1 (fr)
SG (1) SG11202000230VA (fr)
TN (1) TN2020000001A1 (fr)
TW (1) TW201920081A (fr)
UY (1) UY37806A (fr)
WO (1) WO2019014352A1 (fr)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105026373B (zh) 2013-01-31 2018-03-30 沃泰克斯药物股份有限公司 作为钠通道调节剂的吡啶酮酰胺
GEP20207102B (en) 2013-07-19 2020-05-11 Vertex Pharma Sulfonamides as modulators of sodium channels
RS57700B1 (sr) 2013-12-13 2018-12-31 Vertex Pharma Prolekovi piridonskih amida korisni kao modulatori kanala za natrijum
MX2019013574A (es) 2017-05-16 2019-12-18 Vertex Pharma Amidas de piridona deuteradas y sus profarmacos como moduladores de los canales de sodio.
JP7277431B2 (ja) 2017-07-11 2023-05-19 バーテックス ファーマシューティカルズ インコーポレイテッド ナトリウムチャネルのモジュレーターとしてのカルボキサミド
JP2021512935A (ja) 2018-02-12 2021-05-20 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated 疼痛を処置する方法
AR114254A1 (es) 2018-02-15 2020-08-12 Vertex Pharma Moduladores del regulador de conductancia transmembrana de fibrosis quística, composiciones farmacéuticas, métodos de tratamiento y proceso de preparación de los moduladores
US20220227732A1 (en) * 2018-07-09 2022-07-21 Lieber Institute, Inc. Pyridine carboxamide compounds for inhibiting nav1.8
CA3105748A1 (fr) 2018-07-09 2020-01-16 Lieber Institute, Inc. Composes pyridazineg pour inhiber nav1.8
US20210387966A1 (en) * 2018-11-02 2021-12-16 Merck Sharp & Dohme Corp. 2-amino-n-heteroaryl-nicotinamides as nav1.8 inhibitors
US20220110923A1 (en) * 2019-01-10 2022-04-14 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
WO2020146682A1 (fr) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Carboxamides utilisés en tant que modulateurs de canaux sodiques
WO2020151728A1 (fr) * 2019-01-25 2020-07-30 江苏恒瑞医药股份有限公司 Derive de 2-oxo-1,2-dihydropyridine, son procede de preparation et ses applications medicales
WO2020176763A1 (fr) 2019-02-27 2020-09-03 Vertex Pharmaceuticals Incorporated Forme posologique comprenant un promédicament inhibiteur de canal sodique na 1,8
WO2020219867A1 (fr) 2019-04-25 2020-10-29 Vertex Pharmaceuticals Incorporated Compositions de co-cristaux d'amide de pyridone pour le traitement de la douleur
TW202120517A (zh) 2019-08-14 2021-06-01 美商維泰克斯製藥公司 製備cftr調節劑之方法
JP2022544383A (ja) 2019-08-14 2022-10-18 バーテックス ファーマシューティカルズ インコーポレイテッド Cftrモジュレータの結晶形態
TW202115038A (zh) * 2019-08-19 2021-04-16 大陸商江蘇恆瑞醫藥股份有限公司 苯甲醯胺稠芳環類衍生物、其製備方法及其在醫藥上的應用
US20230303495A9 (en) * 2019-09-12 2023-09-28 Orion Corporation Pyridine oxynitride, preparation method therefor and use thereof
CA3164134A1 (fr) 2019-12-06 2021-06-10 Vertex Pharmaceuticals Incorporated Tetrahydrofuranes substitues en tant que modulateurs de canaux sodiques
CN110950797A (zh) * 2019-12-06 2020-04-03 丽水绿氟科技有限公司 一种2-三氟甲基-3-氟-4-吡啶甲酸及其衍生物的制备方法
CN110937994B (zh) * 2019-12-10 2022-04-22 浙江大洋生物科技集团股份有限公司 二步氯化法合成2,4-二氯-6-氟苯甲酰氯的方法
CN114437062B (zh) * 2020-04-30 2024-05-17 成都海博为药业有限公司 一种可作为钠通道调节剂的化合物及其用途
EP4146628A1 (fr) 2020-05-06 2023-03-15 Bayer Aktiengesellschaft Pyridine (thio)amides en tant que composés fongicides
US20230180756A1 (en) 2020-05-12 2023-06-15 Bayer Aktiengesellschaft Triazine and pyrimidine (thio)amides as fungicidal compounds
MX2022015581A (es) 2020-06-17 2023-01-24 Merck Sharp & Dohme Llc 2-oxoimidazolidin-4-carboxamidas como inhibidores de nav1.8.
CN113880771B (zh) * 2020-07-03 2023-09-19 福建盛迪医药有限公司 一种选择性Nav抑制剂的结晶形式及其制备方法
CN111920796A (zh) * 2020-08-28 2020-11-13 南京医科大学 化合物在制备治疗癫痫药物中的应用
CN111808019B (zh) * 2020-09-08 2020-11-27 上海济煜医药科技有限公司 一种并环化合物及其应用
CN114031518B (zh) * 2020-12-08 2023-08-18 成都海博为药业有限公司 一种苄胺或苄醇衍生物及其用途
KR20240019064A (ko) 2021-03-11 2024-02-14 상하이 제민케어 파마슈티칼 컴퍼니 리미티드 피리딘 질소 산화물 화합물의 결정 형태 및 이의 용도
IL307338A (en) 2021-04-05 2023-11-01 Bristol Myers Squibb Co Pyridinyl substituted oxisoisoindoline compounds for cancer therapy
CA3217565A1 (fr) 2021-05-07 2022-11-10 Ashok Arasappan Cycloalkyl 3-oxopiperazine carboxamides et cycloheteroalkyle 3-oxopiperazine carboxamides en tant qu'inhibiteurs de nav1.8
JP2024520649A (ja) 2021-06-04 2024-05-24 バーテックス ファーマシューティカルズ インコーポレイテッド (2r,3s,4s,5r)-4-[[3-(3,4-ジフルオロ-2-メトキシ-フェニル)-4,5-ジメチル-5-(トリフルオロメチル)テトラヒドロフラン-2-カルボニル]アミノ]ピリジン-2-カルボキサミドを含む固体剤形及び投与レジメン
CN117858875A (zh) 2021-06-04 2024-04-09 沃泰克斯药物股份有限公司 羟基和(卤代)烷氧基取代的四氢呋喃作为钠通道调节剂
EP4347583A1 (fr) 2021-06-04 2024-04-10 Vertex Pharmaceuticals Incorporated Analogues de tétrahydrofurane substitués utiles en tant que modulateurs de canaux sodiques
EP4347031A1 (fr) 2021-06-04 2024-04-10 Vertex Pharmaceuticals Incorporated N-(hydroxyalkyl (hétéro)aryl) tétrahydrofuran carboxamides utilisés en tant que modulateurs de canaux sodiques
WO2022256660A1 (fr) * 2021-06-04 2022-12-08 Vertex Pharmaceuticals Incorporated Procédé de synthèse de modulateurs de tétrahydrofurane substitués de canaux sodiques
EP4347584A1 (fr) 2021-06-04 2024-04-10 Vertex Pharmaceuticals Incorporated Analogues de n-(hydroxyalkyl(hétéro)aryl)tétrahydrofurane carboxamide en tant que modulateurs de canaux sodiques
CA3221788A1 (fr) 2021-06-04 2022-12-08 Vertex Pharmaceuticals Incorporated Tetrahydrofuran-2-carboxamides substitues utiles en tant que modulateurs de canaux sodiques
AR126670A1 (es) 2021-08-02 2023-11-01 Eurofarma Laboratorios S A COMPUESTOS N-ACILIDRAZÓNICOS INHIBIDORES DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, COMPOSICIONES, USOS, MÉTODOS DE TRATAMIENTO DE ESTOS Y KITS
AR126669A1 (es) 2021-08-02 2023-11-01 Eurofarma Laboratorios S A COMPUESTOS N-ACILIDRAZÓNICOS INHIBIDORES DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, COMPOSICIONES, USOS, MÉTODOS DE TRATAMIENTO DE ESTOS Y KITS
EP4455130A1 (fr) 2022-01-18 2024-10-30 Chengdu Kanghong Pharmaceutical Co., Ltd. Inhibiteur de nav1.8 à cycle condensé aromatique et son utilisation
WO2023186102A1 (fr) * 2022-04-02 2023-10-05 武汉人福创新药物研发中心有限公司 Inhibiteur de nav1.8 et son utilisation
WO2023205468A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryle pour le traitement de la douleur
AU2023256603A1 (en) 2022-04-22 2024-11-07 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
TW202408501A (zh) 2022-04-22 2024-03-01 美商維泰克斯製藥公司 用於治療疼痛之雜芳基化合物
WO2023205465A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
WO2023207949A1 (fr) * 2022-04-25 2023-11-02 中国科学院上海药物研究所 Composé cyclique fusionné et son utilisation
WO2023211990A1 (fr) 2022-04-25 2023-11-02 Siteone Therapeutics, Inc. Inhibiteurs d'amides hétérocycliques bicycliques de na v1.8 pour le traitement de la douleur
WO2023246867A1 (fr) * 2022-06-22 2023-12-28 武汉人福创新药物研发中心有限公司 Inhibiteur de nav1.8
TW202409017A (zh) * 2022-08-24 2024-03-01 大陸商江蘇恆瑞醫藥股份有限公司 雜環類化合物、其製備方法及其在醫藥上的應用
WO2024046253A1 (fr) * 2022-08-28 2024-03-07 上海汇伦医药股份有限公司 Régulateur de canal sodique et son utilisation
WO2024046409A1 (fr) * 2022-08-31 2024-03-07 江苏恒瑞医药股份有限公司 Composé hétérocyclique, son procédé de préparation et son utilisation pharmaceutique
WO2024054622A2 (fr) * 2022-09-09 2024-03-14 Latigo Biotherapeutics, Inc. Composés bloquant les canaux sodiques, leurs dérivés et leurs procédés d'utilisation
WO2024123815A1 (fr) 2022-12-06 2024-06-13 Vertex Pharmaceuticals Incorporated Procédé de synthèse de modulateurs de tétrahydrofurane substitués de canaux sodiques
WO2024146632A1 (fr) * 2023-01-06 2024-07-11 西藏海思科制药有限公司 Dérivé de tétrahydrothiophène et son utilisation en médecine
WO2024153856A1 (fr) * 2023-01-18 2024-07-25 Orion Corporation Procédé de préparation de 3- (4,5-dichloro-2-(4- (trifluorométhoxy)phénoxy)benzamido)pyridine 1-oxyde
CN118324743A (zh) * 2023-04-19 2024-07-12 中国科学院上海药物研究所 Nav1.8抑制剂及其制备方法和用途

Family Cites Families (249)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1025305A (en) 1910-07-29 1912-05-07 Andrew Rasmussen Feeding means for power hacksaw-machines.
US1008714A (en) 1910-12-27 1911-11-14 Henry M Hammer Delinting-machine.
US2511231A (en) 1949-03-26 1950-06-13 Eastman Kodak Co 1-cyanophenyl-3-acylamino-5-pyrazolone couplers for color photography
US2688617A (en) 1951-07-17 1954-09-07 American Cyanamid Co Sulfonated dihalogeno diaminostilbenes
US2657134A (en) 1951-12-05 1953-10-27 Eastman Kodak Co Photographic emulsion with colored couplers containing isophthalic ester groups
BE516025A (fr) 1951-12-05
US2725292A (en) 1952-05-15 1955-11-29 Eastman Kodak Co Colored couplers containing solubilizing groups
US2710802A (en) 1953-03-16 1955-06-14 Eastman Kodak Co Dialkyl-5-(oxanilamido) isophthalate couplers for color photography
US2710803A (en) 1953-03-26 1955-06-14 Eastman Kodak Co Color couplers containing hydroxyalkyl groups
BE528163A (fr) 1953-04-17
BE531589A (fr) 1953-09-02
US4218765A (en) 1974-10-03 1980-08-19 Standard Oil Company (Indiana) Two-dimensional frequency domain filtering
DE2623228C3 (de) 1976-05-24 1981-09-10 Ludwig Merckle Kg Chem. Pharm. Fabrik, 7902 Blaubeuren N-Acyl-substituierte Benzamide, Verfahren zu ihrer Herstellung und Arzneimittel, enthaltend solche Benzamide
US4639273A (en) 1983-05-06 1987-01-27 Morton Thiokol, Inc. Asphalt-adhesion improving additives prepared by formaldehyde condensation with polyamines
JPS63182182A (ja) 1987-01-23 1988-07-27 Fuji Photo Film Co Ltd 感熱記録材料
FR2628864B1 (fr) 1988-03-21 1990-06-15 France Etat Procede de segmentation d'un champ de vecteurs vitesse, notamment de vitesses de deplacement de points d'une image dans une sequence d'images
KR920701167A (ko) 1989-07-07 1992-08-11 에릭 에스. 딕커 약제학적 활성 화합물
JP2766323B2 (ja) 1989-07-19 1998-06-18 株式会社東芝 表示調整装置
US5304121A (en) 1990-12-28 1994-04-19 Boston Scientific Corporation Drug delivery system making use of a hydrogel polymer coating
DE4019307A1 (de) 1990-06-16 1991-12-19 Bayer Ag 2-methoximinocarbonsaeureester
US5258407A (en) 1991-12-31 1993-11-02 Sterling Winthrop Inc. 3,4-disubstituted phenols-immunomodulating agents
US5449691A (en) 1991-12-31 1995-09-12 Sterling Winthrop Inc. 3,4-disubstituted anilines-immunomodulating agents
FR2687932A1 (fr) 1992-02-27 1993-09-03 Oreal Dispersion huile-dans-l'eau susceptible de former des films composites.
JPH05313169A (ja) 1992-05-08 1993-11-26 Fuji Photo Film Co Ltd 液晶配向膜
HUT63941A (en) 1992-05-15 1993-11-29 Hoechst Ag Process for producing 4-alkyl-substituted pyrimidine-5-carboxanilide derivatives, and fungicidal compositions comprising same
US5886026A (en) 1993-07-19 1999-03-23 Angiotech Pharmaceuticals Inc. Anti-angiogenic compositions and methods of use
GB9408185D0 (en) 1994-04-25 1994-06-15 Fujisawa Pharmaceutical Co New benzamide derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same
JP3668494B2 (ja) 1994-05-31 2005-07-06 帝人株式会社 ナフタレン誘導体
US5536718A (en) 1995-01-17 1996-07-16 American Cyanamid Company Tricyclic benzazepine vasopressin antagonists
AR002459A1 (es) 1995-01-17 1998-03-25 American Cyanamid Co Antagonistas de vasopresina de benzacepina triciclicos, una composicion farmaceutica que los contiene, un metodo para tratar enfermedades y unprocedimiento para su preparacion.
US5532235A (en) 1995-01-17 1996-07-02 American Cyanamid Company Tricyclic benzazepine vasopressin antagonists
US5753648A (en) 1995-01-17 1998-05-19 American Cyanamid Company Tricyclic benzazepine vasopressin antagonists
US6099562A (en) 1996-06-13 2000-08-08 Schneider (Usa) Inc. Drug coating with topcoat
DE19523640A1 (de) 1995-06-29 1997-01-02 Bayer Ag Substituierte Carbonylaminophenyluracile
DE19621522A1 (de) 1996-05-29 1997-12-04 Hoechst Schering Agrevo Gmbh Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung
JP3731963B2 (ja) 1997-01-14 2006-01-05 株式会社シマノ 釣り竿用口栓
JPH10213820A (ja) 1997-01-31 1998-08-11 Canon Inc 液晶素子及び液晶装置
ES2205472T3 (es) 1997-04-22 2004-05-01 Neurosearch A/S Derivados de fenilo sustituidos, su preparacion y uso.
CA2319493A1 (fr) 1998-03-18 1999-09-23 Regine Bohacek Inhibiteurs de transduction de signaux heterocycliques et compositions les contenant
AU3665199A (en) 1998-04-29 1999-11-16 Vertex Pharmaceuticals Incorporated Inhibitors of impdh enzyme
JP2002179651A (ja) 1998-06-19 2002-06-26 Wakamoto Pharmaceut Co Ltd ベンズアニリド誘導体及び医薬組成物
CA2342626A1 (fr) 1998-10-22 2000-05-04 Neurosearch A/S Derives de phenyle substitue, leur preparation et leur application
SK15522001A3 (sk) 1999-04-28 2002-06-04 Aventis Pharma Deutschland Gmbh Deriváty kyselín s tromi arylovými zvyškami ako ligandy receptorov PPAR a farmaceutické kompozície, ktoré ich obsahujú
WO2001007028A2 (fr) 1999-07-23 2001-02-01 Allergan Sales, Inc. Utilisation d'antagonistes de recepteurs de retinoides dans le traitement du cancer de la prostate
AU780787B2 (en) 1999-09-17 2005-04-14 Millennium Pharmaceuticals, Inc. Benzamides and related inhibitors of factor Xa
US6531291B1 (en) 1999-11-10 2003-03-11 The Trustees Of Columbia University In The City Of New York Antimicrobial activity of gemfibrozil and related compounds and derivatives and metabolites thereof
US20030114482A1 (en) 1999-12-15 2003-06-19 Maurizio Pacifici Use of retinoid receptor antagonists or agonists in the treatment of cartilage and bone pathologies
US6313168B1 (en) 1999-12-15 2001-11-06 Allergan Sales, Inc. Use of retinoid receptor antagonists in the treatment of cartilage and bone pathologies
WO2001056989A2 (fr) 2000-02-01 2001-08-09 Cor Therapeutics, Inc. INHIBITEURS DU FACTEUR Xa CONTENANT DU PHENYLENE BIVALENT
WO2001064643A2 (fr) 2000-02-29 2001-09-07 Cor Therapeutics, Inc. Benzamides et inhibiteurs associes du facteur xa
CA2402315A1 (fr) 2000-03-09 2001-09-13 Michael Jaye Utilisations therapeutiques des mediateurs ppar
MY138097A (en) 2000-03-22 2009-04-30 Du Pont Insecticidal anthranilamides
DE10033337A1 (de) * 2000-07-08 2002-01-17 Boehringer Ingelheim Pharma Biphenylcarbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel
US20020032238A1 (en) * 2000-07-08 2002-03-14 Henning Priepke Biphenylcarboxylic acid amides, the preparation thereof and the use thereof as medicaments
WO2002028835A1 (fr) 2000-10-05 2002-04-11 Fujisawa Pharmaceutical Co., Ltd. Composés à base de benzamide, inhibiteurs des sécrétions d'apolipoprotéine b
AU1339302A (en) 2000-10-20 2002-05-06 Biocryst Pharm Inc Biaryl compounds as serine protease inhibitors
WO2002042273A2 (fr) 2000-11-07 2002-05-30 Bristol-Myers Squibb Company Derives d'acide utiles comme inhibiteurs de serines proteases
AU2002224115A1 (en) 2000-11-28 2002-06-11 Yamanouchi Pharmaceutical Co., Ltd. 1,4,5,6-tetrahydroimidazo(4,5-d)diazepine derivatives or salts thereof
HUP0302604A3 (en) 2000-12-06 2005-09-28 Aventis Pharma Gmbh Guanidine and amidine derivatives as factor xa inhibitors
WO2002051397A1 (fr) 2000-12-22 2002-07-04 Ishihara Sangyo Kaisha, Ltd. Derives d'aniline ou sels de ceux-ci, ainsi qu'inhibiteurs de production de cytokine contenant ces derives
EP1217000A1 (fr) 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibiteurs du factor Xa et factor VIIa
WO2002054077A2 (fr) 2000-12-29 2002-07-11 7Tm Pharma A/S Validation de molecules biologiques en tant que cibles de medicaments au moyen de chelates d'ions metalliques chez des modeles d'animaux de laboratoire
ES2364550T3 (es) 2001-03-05 2011-09-06 E. I. Du Pont De Nemours And Company Agentes de control de plagas de invertebrados de diamidas heterocíclicas.
JP4342178B2 (ja) 2001-04-06 2009-10-14 バイオクリスト・ファマシューティカルズ インク. セリンプロテアーゼ阻害剤としてのビアリール化合物
EP1383760A1 (fr) 2001-04-30 2004-01-28 Fujisawa Pharmaceutical Co., Ltd. Composes biarylcarboxamide comme inhibiteurs d'apolipoproteine b
WO2002098839A1 (fr) 2001-06-01 2002-12-12 Tanabe Seiyaku Co., Ltd. Biphenylcarboxamides et procede de preparation de ceux-ci
WO2002101007A2 (fr) 2001-06-13 2002-12-19 Genesoft Pharmaceuticals, Inc Composes benzamides anti-pathogenes
WO2003003009A1 (fr) 2001-06-29 2003-01-09 7Tm Pharma A/S Utilisation de chelates a ions metalliques dans la validation de molecules biologiques utilisees comme cibles medicamenteuses dans des modeles animaux experimentaux
WO2003003008A1 (fr) 2001-06-29 2003-01-09 7Tm Pharma A/S Bibliotheques chimiques utiles aux procedes de decouvertes de medicaments
DE10132686A1 (de) 2001-07-05 2003-01-16 Boehringer Ingelheim Pharma Heteroarylcarbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel
WO2003007955A2 (fr) 2001-07-20 2003-01-30 Cancer Research Technology Limited Nouvelle utilisation
WO2003013516A1 (fr) 2001-08-10 2003-02-20 Adipogenix, Inc. Composes servant a moduler l'accumulation des graisses
AUPR738301A0 (en) 2001-08-30 2001-09-20 Starpharma Limited Chemotherapeutic agents
WO2003045921A1 (fr) 2001-11-28 2003-06-05 Fujisawa Pharmaceutical Co., Ltd. Composes d'amide heterocycliques en tant qu'inhibiteurs de l'apolipoproteine b
WO2003055477A1 (fr) 2001-12-21 2003-07-10 7Tm Pharma A/S Methode de traitement de troubles lies au recepteur de la melanocortine (mc), faisant intervenir un chelate et/ou un chelateur
EP1465613A2 (fr) 2002-01-10 2004-10-13 Boehringer Ingelheim Pharma GmbH & Co. KG Combinaison d'inhibiteurs de mtp ou d'inhibiteurs de secretions apob avec des fibrates en vue d'une utilisation comme medicament
BR0307167A (pt) 2002-01-22 2005-02-09 Du Pont Composto, método e composição de controle de pragas invertebradas
CN1630629B (zh) 2002-02-28 2010-05-05 日本烟草产业株式会社 酯化合物及其医药用途
NZ535614A (en) 2002-03-11 2006-10-27 Tibotec Pharm Ltd Small molecule entry inhibitors
US6875780B2 (en) 2002-04-05 2005-04-05 Warner-Lambert Company Compounds that modulate PPAR activity and methods for their preparation
JP2004043456A (ja) 2002-05-24 2004-02-12 Yamanouchi Pharmaceut Co Ltd ベンゾアゼピン誘導体又はその塩を有効成分とする医薬
JP2003342175A (ja) 2002-05-24 2003-12-03 Yamanouchi Pharmaceut Co Ltd 新規なベンゾアゼピン誘導体又はその塩を有効成分とするメニエール病治療剤
AU2003245669A1 (en) 2002-06-21 2004-01-06 Cellular Genomics, Inc. Certain aromatic monocycles as kinase modulators
CN1703395A (zh) 2002-08-09 2005-11-30 特兰斯泰克制药公司 芳基和杂芳基化合物以及调节凝血的方法
US20040110802A1 (en) 2002-08-23 2004-06-10 Atli Thorarensen Antibacterial benzoic acid derivatives
JP2004175739A (ja) 2002-11-28 2004-06-24 Tanabe Seiyaku Co Ltd 医薬組成物
ATE553076T1 (de) 2002-12-12 2012-04-15 Basf Se Aminosubstituierte hydroxyphenylbenzophenonderivate
BR0317323A (pt) * 2002-12-20 2005-11-16 Pfizer Prod Inc Inibidores de proteìna de transferência de triglicerìdeos microssomal
SG159388A1 (en) 2003-01-08 2010-03-30 Chiron Corp Antibacterial agents
AR043633A1 (es) 2003-03-20 2005-08-03 Schering Corp Ligandos de receptores de canabinoides
JP2004315395A (ja) 2003-04-14 2004-11-11 Yamanouchi Pharmaceut Co Ltd 新規な安息香酸誘導体又はその塩
WO2005000309A2 (fr) 2003-06-27 2005-01-06 Ionix Pharmaceuticals Limited Composes chimiques
MXPA06002853A (es) 2003-09-11 2006-06-14 Kemia Inc Inhibidores citoquina.
WO2005033079A1 (fr) 2003-09-30 2005-04-14 Eisai Co., Ltd. Agent antifongique a compose heterocyclique
JPWO2005040135A1 (ja) 2003-10-24 2007-03-08 小野薬品工業株式会社 抗ストレス薬およびその医薬用途
BR122015015718B1 (pt) 2004-01-28 2016-05-10 Mitsui Chemicals Inc derivados de amida
DE102004009238A1 (de) 2004-02-26 2005-09-08 Merck Patent Gmbh Arylamid-Derivate
US7427390B2 (en) 2004-03-10 2008-09-23 Schering Ag Radiohalogenated benzamide derivatives and their use in tumor diagnosis and tumor therapy
WO2006007864A1 (fr) 2004-07-17 2006-01-26 Max Planck Geselllschaft Zur Förderung Der Wissenschaft Traitement d'etats neurodegeneratifs
AU2005266090A1 (en) 2004-07-23 2006-02-02 Pfizer Inc. Pyridine derivatives
DE102004050196A1 (de) 2004-10-15 2006-04-20 Sanofi-Aventis Deutschland Gmbh Substituierte 2-Pyridon-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Medikament
MX2007006109A (es) 2004-12-01 2007-10-04 Devgen Nv Derivados de tiazol sustituidos en 5-carboxamido que interactuan con canales de iones, en particular con canales ionicos de la familia de kv.
WO2006067445A2 (fr) 2004-12-22 2006-06-29 Astrazeneca Ab Composes chimiques
WO2006068199A1 (fr) 2004-12-22 2006-06-29 Mochida Pharmaceutical Co., Ltd. Dérivés de 3-oxy-1,2,4-triazole métaboliquement stables
SG138768A1 (en) 2005-06-21 2008-02-29 Mitsui Chemicals Inc Amide derivative and pesticide containing such compound
MX2007016070A (es) 2005-07-07 2008-03-10 Abbott Lab Promotores de apoptosis.
JP4580836B2 (ja) 2005-07-25 2010-11-17 三井化学アグロ株式会社 殺虫殺菌組成物
BRPI0615948A2 (pt) 2005-09-07 2011-05-31 Plexxikon Inc composto ativo de ppar, sua composição, seu kit e seu uso
EP1942732A2 (fr) 2005-11-02 2008-07-16 Cytokinetics, Inc. Entites et compositions chimiques et methodes associees
WO2007052843A1 (fr) 2005-11-04 2007-05-10 Takeda Pharmaceutical Company Limited Compose amide heterocyclique et son utilisation
EP1966184B1 (fr) 2005-12-20 2010-08-25 NeuroSearch A/S Derives de pyridinyl-quinazoline et leur utilisation medicale
UY30117A1 (es) 2006-01-31 2007-06-29 Tanabe Seiyaku Co Compuesto amina trisustituido
US7351434B2 (en) 2006-04-07 2008-04-01 Academia Sinica Therapeutic Gastrodia extracts
AU2007238857B2 (en) 2006-04-11 2013-05-02 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of voltage-gated sodium channels
EP2073806B1 (fr) 2006-10-12 2012-02-15 Xenon Pharmaceuticals Inc. Utilisation de composés de spiro-oxindole comme agents thérapeutiques
WO2008044767A1 (fr) 2006-10-13 2008-04-17 Takeda Pharmaceutical Company Limited Dérivé d'amine aromatique et utilisation de celui-ci
JP2008106017A (ja) 2006-10-27 2008-05-08 Tokyo Univ Of Science Oatp選択的阻害性を有する化合物、及び該化合物を含むoatpの選択的阻害剤
SG10201504425SA (en) 2006-12-08 2015-07-30 Millennium Pharm Inc Unit dose formulations and methods of treating thrombosis with an oral factor xa inhibitor
GB0625659D0 (en) 2006-12-21 2007-01-31 Cancer Rec Tech Ltd Therapeutic compounds and their use
JP4325681B2 (ja) 2007-02-13 2009-09-02 ソニー株式会社 固体撮像装置、撮像装置
CN101622231B (zh) 2007-02-28 2013-12-04 艾德维纳斯医疗私人有限公司 作为葡糖激酶激活剂的2,2,2-三取代的乙酰胺衍生物、它们的制造方法和药学应用
WO2008135826A2 (fr) 2007-05-03 2008-11-13 Pfizer Limited Dérivés de la pyridine
WO2008140810A1 (fr) 2007-05-11 2008-11-20 Cytokinetics, Incorporated Certaines entités chimiques, compositions et procédés
EP2167058B1 (fr) 2007-06-18 2015-08-12 University Of Louisville Research Foundation, Inc. Famille d'inhibiteurs de pfkfb3 à activités anti-néoplasiques
WO2009000413A1 (fr) 2007-06-26 2008-12-31 Sanofi-Aventis Synthèse régiosélective catalysée par le cuivre de benzimidazoles et d'azabenzimidazoles
US20090012091A1 (en) 2007-07-02 2009-01-08 Kinagen, Inc. Oximide derivatives and their therapeutical application
US8512934B2 (en) 2007-10-10 2013-08-20 Basf Se Sulphonium salt initiators
CN101952269B (zh) 2007-10-10 2014-06-25 巴斯夫欧洲公司 锍盐引发剂
MX2010003865A (es) 2007-10-11 2010-06-01 Vertex Pharma Aril amidas utiles como inhibidores de canales de sodio dependientes de voltaje.
CA2701766A1 (fr) 2007-10-11 2009-04-16 Vertex Pharmaceuticals Incorporated Amides utiles en tant qu'inhibiteurs de canaux sodiques sensibles au voltage
JP5555169B2 (ja) 2007-10-11 2014-07-23 バーテックス ファーマシューティカルズ インコーポレイテッド 電位開口型ナトリウムチャネルの阻害剤として有用なヘテロアリールアミド
JP2009108152A (ja) 2007-10-29 2009-05-21 Sumitomo Chemical Co Ltd 重合性化合物および光学フィルム
WO2009070533A1 (fr) 2007-11-29 2009-06-04 Complegen, Inc. Procédés d'inhibition de stéaroyle-coa désaturase
JP2009149754A (ja) 2007-12-20 2009-07-09 Sumitomo Chemical Co Ltd 重合性化合物および該重合性化合物を重合してなる光学フィルム
EP2219646A4 (fr) 2007-12-21 2010-12-22 Univ Rochester Procédé permettant de modifier la durée de vie d'organismes eucaryotes
JP2009209090A (ja) 2008-03-04 2009-09-17 Mitsui Chemicals Inc 殺虫剤及び該殺虫剤に含まれる化合物、並びに該化合物の使用方法
US20100009970A1 (en) 2008-03-19 2010-01-14 Combinatorx (Singapore) Pte. Ltd. Compositions and methods for treatment of viral diseases
JP5219583B2 (ja) 2008-03-31 2013-06-26 住友化学株式会社 組成物、光学フィルムとその製造方法、光学部材及び表示装置
JP2010001284A (ja) 2008-05-20 2010-01-07 Sumitomo Chemical Co Ltd 化合物及び光学フィルム
KR20160079934A (ko) 2008-06-16 2016-07-06 유니버시티 오브 테네시 리서치 파운데이션 암 치료용 화합물
ES2797955T3 (es) 2008-08-25 2020-12-04 Novartis Ag Moduladores de la ruta de hedgehog
JP5443720B2 (ja) 2008-09-05 2014-03-19 住友化学株式会社 組成物、光学フィルム及びその製造方法、光学部材ならびに表示装置
JP2010066630A (ja) 2008-09-12 2010-03-25 Sumitomo Chemical Co Ltd 光学フィルムの製造方法及び光学フィルム
US8354444B2 (en) 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
MY160424A (en) 2008-09-18 2017-03-15 Hoffmann La Roche Substituted pyrrolidine-2-carboxyamides.
WO2010048149A2 (fr) 2008-10-20 2010-04-29 Kalypsys, Inc. Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie
JP5649779B2 (ja) 2008-11-28 2015-01-07 住友化学株式会社 液晶性組成物及び光学フィルム
AU2009331179B2 (en) 2008-12-26 2014-09-18 Sumitomo Pharma Co., Ltd. Novel bicyclic heterocyclic compound
TWI482769B (zh) 2009-03-16 2015-05-01 Sumitomo Chemical Co 化合物、光學膜片及光學膜片之製造方法
JP5899607B2 (ja) 2009-03-16 2016-04-06 住友化学株式会社 化合物、光学フィルム及び光学フィルムの製造方法
AR076880A1 (es) 2009-05-18 2011-07-13 Orion Corp Inhibidores de proteasa, composiciones farmaceuticas que los contienen y su uso.
EP2253617A1 (fr) 2009-05-20 2010-11-24 Bayer CropScience AG Composés halogénés comme pesticides
WO2010138901A1 (fr) 2009-05-29 2010-12-02 Biogen Idec Ma Inc Composés contenant de l'acide carboxylique, leurs dérivés et procédés d'utilisation associés
JP2011006360A (ja) 2009-06-26 2011-01-13 Sumitomo Chemical Co Ltd 化合物、光学フィルム及び光学フィルムの製造方法
AR077252A1 (es) 2009-06-29 2011-08-10 Xenon Pharmaceuticals Inc Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos
KR101256018B1 (ko) 2009-08-20 2013-04-18 한국과학기술연구원 단백질 키나아제 저해활성을 갖는 1,3,6-치환된 인돌 화합물
WO2011026240A1 (fr) 2009-09-04 2011-03-10 Zalicus Pharmaceuticals Ltd. Dérivés d'oxopipérazine pour le traitement de la douleur et de l'épilepsie
US20120189670A1 (en) 2009-09-14 2012-07-26 Kirkpatrick D Lynn Pharmaceutical compositions and formulations including inhibitors of the pleckstrin homology domain and methods for using same
US8420647B2 (en) 2010-01-21 2013-04-16 Hoffmann-La Roche Inc. 4-phenoxy-nicotinamide or 4-phenoxy-pyrimidine-5-carboxamide compounds
JP5375644B2 (ja) 2010-02-10 2013-12-25 住友化学株式会社 組成物及び光学フィルム
CN104592205A (zh) 2010-03-01 2015-05-06 Gtx公司 用于治疗癌的化合物
JP2013525368A (ja) 2010-04-23 2013-06-20 キネタ・インコーポレイテツド 抗ウイルス性化合物
EP2563759B1 (fr) 2010-04-27 2022-04-06 Calcimedica, Inc. Composés qui modulent le calcium intracellulaire
US8598164B2 (en) 2010-05-06 2013-12-03 Vertex Pharmaceuticals Incorporated Heterocyclic chromene-spirocyclic piperidine amides as modulators of ion channels
WO2012016133A2 (fr) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
EP2616453A4 (fr) 2010-08-24 2014-07-02 Univ Brigham Young Composés antimétastatiques
US20130225870A1 (en) 2010-08-25 2013-08-29 Synta Pharmaceuticals Corp. Method of synthesizing substituted 2-alkyl phenols
ES2650744T3 (es) 2010-12-14 2018-01-22 Electrophoretics Limited Inhibidores de la caseína quinasa 1 delta (CK1delta)
EP2670752B1 (fr) 2011-02-02 2016-03-16 Vertex Pharmaceuticals Incorporated Amides de pipéridine spirocyclique-pyrrolopyrazine en tant que modulateurs de canaux ioniques
CA2827311A1 (fr) 2011-02-18 2012-08-23 Vertex Pharmaceuticals Incorporated Amides de piperidine spirocyclique chromanique en tant que modulateurs des canaux ioniques
ES2786298T3 (es) 2011-03-03 2020-10-09 Zalicus Pharmaceuticals Ltd Inhibidores de benzimidazol del canal de sodio
JP6088443B2 (ja) 2011-03-14 2017-03-01 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated イオンチャネルのモジュレーターとしてのモルホリン−スピロ環式ピペリジンアミド
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
US9278910B2 (en) 2011-05-31 2016-03-08 Receptos, Inc. GLP-1 receptor stabilizers and modulators
JP2014520151A (ja) 2011-06-20 2014-08-21 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー 蠕虫感染を処置するためのヘテロ環式化合物
JP2014527036A (ja) 2011-06-27 2014-10-09 ザ ジャクソン ラボラトリー 癌および自己免疫疾患の処置のための方法および組成物
PT2573073E (pt) 2011-09-26 2015-02-05 Sanofi Sa Derivados de pirazoloquinolinona, sua preparação e sua utilização terapêutica
CN103012397B (zh) 2011-09-26 2017-03-01 赛诺菲 吡唑并喹啉酮衍生物、其制备方法及其治疗用途
US9169246B2 (en) 2011-09-26 2015-10-27 Sanofi Pyrazoloquinolinone derivatives, preparation thereof and therapeutic use thereof
BR112014009102A2 (pt) 2011-10-26 2017-04-18 Pfizer Ltd compostos químicos
GB201119799D0 (en) 2011-11-16 2011-12-28 Sentinel Oncology Ltd Pharmaceutical compounds
WO2013086229A1 (fr) 2011-12-07 2013-06-13 Amgen Inc. Inhibiteurs aryle et hétéroaryle bicycliques des canaux calciques
EP2606726A1 (fr) 2011-12-21 2013-06-26 Bayer CropScience AG Dérivés de trifluoroéthylsulfure substitués par du N-arylamidine en tant qu'acaricides et insecticides
EA201491260A1 (ru) 2011-12-23 2014-11-28 Новартис Аг Соединения и композиции для ингибирования взаимодействия bcl2 с партнерами по связыванию
JP6215230B2 (ja) 2012-01-16 2017-10-18 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated イオンチャネルのモジュレーターとしてのピラン−スピロ環式ピペリジンアミド
WO2013114250A1 (fr) 2012-02-03 2013-08-08 Pfizer Inc. Dérivés d'imidazopyridine et de benziimidazole en tant que modulateurs du canal sodium
WO2013131018A1 (fr) 2012-03-02 2013-09-06 Zalicus Pharmaceuticals Ltd. Inhibiteurs biaryle du canal sodique
US8980823B2 (en) 2012-03-07 2015-03-17 Shaker A. Mousa Formulations of Factor VIIa inhibitors and utility
US8481479B1 (en) 2012-03-07 2013-07-09 Shaker A. Mousa Formulations of factor VIIa inhibitors and utility
EP2895462A1 (fr) 2012-09-13 2015-07-22 Baden-Württemberg Stiftung gGmbH Inhibiteurs spécifiques de la protéine p21 comme agents thérapeutiques
US20150272939A1 (en) 2012-10-02 2015-10-01 Yale University Identification of Small Molecule Inhibitors of Jumonji AT-Rich Interactive Domain 1A (JARID1A) and 1B (JARID1B) Histone Demethylase
WO2014055644A2 (fr) 2012-10-02 2014-04-10 New York University Compositions pharmaceutique et traitement de maladies génétiques associées à une désintégration d'arn à médiation non-sens
US20140200215A1 (en) 2013-01-15 2014-07-17 Intermune, Inc. Lysophosphatidic acid receptor antagonists
SG11201505952WA (en) 2013-01-31 2015-08-28 Vertex Pharma Quinoline and quinazoline amides as modulators of sodium channels
CA2898653C (fr) * 2013-01-31 2021-09-28 Vertex Pharmaceuticals Incorporated Amides comme modulateurs des canaux sodiques
CN105026373B (zh) 2013-01-31 2018-03-30 沃泰克斯药物股份有限公司 作为钠通道调节剂的吡啶酮酰胺
CN103961348B (zh) 2013-02-05 2016-08-17 上海交通大学医学院 Senp1小分子抑制剂及其应用
WO2014134127A1 (fr) 2013-02-26 2014-09-04 Northeastern University Nitro-esters cannabinergiques et analogues associés
WO2014149207A2 (fr) 2013-03-15 2014-09-25 Dow Agrosciences Llc Compositions insecticides à base de benzimidazole et procédés apparentés
JP5902641B2 (ja) 2013-03-27 2016-04-13 富士フイルム株式会社 光干渉顔料およびその製造方法
JP2014232188A (ja) 2013-05-29 2014-12-11 コニカミノルタ株式会社 セルロースアシレートフィルム、円偏光板及び画像表示装置
WO2014192681A1 (fr) 2013-05-31 2014-12-04 コニカミノルタ株式会社 Composition de résine, élément optique, film optique, plaque de polarisation, plaque de polarisation circulaire et dispositif d'affichage d'image
WO2015030898A2 (fr) 2013-06-07 2015-03-05 The Regents Of The University Of California Commutateurs résonants micromécaniques et pompes de charge
WO2014204831A1 (fr) 2013-06-18 2014-12-24 Merck Sharp & Dohme Corp. Dérivés de nucléosides cycliques à substitution phosphonate et leurs méthodes d'utilisation pour le traitement de maladies virales
CA2917767C (fr) 2013-07-12 2022-05-03 Helmholtz-Zentrum Fur Infektionsforschung Gmbh Cystobactamides
GEP20207102B (en) 2013-07-19 2020-05-11 Vertex Pharma Sulfonamides as modulators of sodium channels
WO2015011284A2 (fr) 2013-07-25 2015-01-29 Fondazione Telethon Inhibiteurs de fapp2 et leurs utilisations
EP3027590A1 (fr) 2013-07-31 2016-06-08 Minoryx Therapeutics S.L. Di(hétéro)arylamides et sulfonamides, procédés permettant leur préparation et utilisations thérapeutiques de ceux-ci
KR101628288B1 (ko) 2013-09-30 2016-06-08 주식회사 엘지화학 음성 광학 분산도를 갖는 광학 소자 제조용 조성물 및 이로부터 제조된 광학 이방체
WO2015085238A1 (fr) 2013-12-05 2015-06-11 The Regents Of The University Of California, A California Corporation Inhibiteurs de lpxc
RS57700B1 (sr) 2013-12-13 2018-12-31 Vertex Pharma Prolekovi piridonskih amida korisni kao modulatori kanala za natrijum
US9204150B2 (en) 2014-02-26 2015-12-01 Intel Corporation Techniques for evaluating compressed motion video quality
WO2015196072A2 (fr) 2014-06-19 2015-12-23 Whitehead Institute For Biomedical Research Utilisations d'inhibiteurs de kinase pour l'induction et le maintien de la pluripotence
WO2016022626A1 (fr) 2014-08-06 2016-02-11 Merck Sharp & Dohme Corp. Antagonistes hétérocycliques des récepteurs cgrp
WO2016040449A1 (fr) 2014-09-10 2016-03-17 Raze Therapeutics, Inc. Inhibiteurs de la 3-phosphoglycérate déshydrogénase) et leurs utilisations
EP2997966A1 (fr) 2014-09-16 2016-03-23 Sanofi Dérivés de pyrrolidine sulfonamide naphtyle en tant que modulateurs KEAP-1 pour le traitement du diabète, l'obésité, de la dyslipidémie et de troubles apparentés
CN106317027A (zh) 2015-06-15 2017-01-11 山东轩竹医药科技有限公司 杂芳基酰胺类衍生物及其作为tgr5激动剂的应用
US11124483B2 (en) 2015-09-02 2021-09-21 The Regents Of The University Of California HER3 ligands and uses thereof
US11413278B2 (en) 2015-10-08 2022-08-16 The Regents Of The University Of California Compounds and methods for promoting stress resistance
CA3001857A1 (fr) 2015-10-14 2017-04-20 Aquinnah Pharmaceuticals, Inc. Composes, compositions et methodes d'utilisation contre des granules de stress
US10781218B2 (en) 2016-03-16 2020-09-22 Kura Oncology, Inc. Substituted inhibitors of menin-MLL and methods of use
US11820932B2 (en) 2016-09-28 2023-11-21 Merck Patent Gmbh Polymerisable liquid crystal material and polymerised liquid crystal film
KR20190063473A (ko) 2016-09-28 2019-06-07 블레이드 테라퓨틱스, 인크. 칼페인 조정자 및 그 치료학적 용도
WO2018161033A1 (fr) 2017-03-02 2018-09-07 Wright, Adrian Inhibiteurs ire1-alpha à petites molécules
CN110785414A (zh) 2017-04-20 2020-02-11 加利福尼亚大学董事会 K-Ras调节剂
WO2018202681A1 (fr) 2017-05-04 2018-11-08 Bayer Cropscience Aktiengesellschaft Utilisation de benzènes disubstitués pour lutter contre des organismes nuisibles résistants aux insecticides
JP2019015998A (ja) 2017-07-03 2019-01-31 東芝テック株式会社 情報処理装置およびプログラム
JP7277431B2 (ja) 2017-07-11 2023-05-19 バーテックス ファーマシューティカルズ インコーポレイテッド ナトリウムチャネルのモジュレーターとしてのカルボキサミド
WO2019018119A1 (fr) 2017-07-18 2019-01-24 Pairnomix, Llc Méthodes de traitement de l'épilepsie et d'affections associées à kcnti
AU2018319016B2 (en) 2017-08-17 2023-08-31 Ikena Oncology, Inc. AHR inhibitors and uses thereof
WO2019150220A1 (fr) 2018-01-30 2019-08-08 Pi Industries Ltd. Nouveaux anthranilamides, leur utilisation en tant qu'insecticides et leurs procédés de préparation
JP2021512935A (ja) 2018-02-12 2021-05-20 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated 疼痛を処置する方法
EP3784753B1 (fr) 2018-04-27 2022-06-08 Merck Patent GmbH Matériau à base de cristaux liquides polymérisable et film à base de cristaux liquides polymérisé
EP3784754B1 (fr) 2018-04-27 2022-06-08 Merck Patent GmbH Matériau à base de cristaux liquides polymérisable et film à base de cristaux liquides polymérisé
WO2019241787A1 (fr) 2018-06-15 2019-12-19 The Regents Of The University Of Colorado A Body Corporate Nouveaux inhibiteurs cycliques de la gmp-amp synthase (cgaz) et leur procédé d'utilisation
SG11202102208WA (en) 2018-09-04 2021-04-29 Magenta Therapeutics Inc Aryl hydrocarbon receptor antagonists and methods of use
AU2019362788A1 (en) 2018-10-15 2021-04-15 Dana-Farber Cancer Institute, Inc. Transcriptional enhanced associate domain (TEAD) transcription factor inhibitors and uses thereof
US12098117B2 (en) 2018-12-11 2024-09-24 Duke University Compositions and methods for the treatment of cancer
WO2020139748A1 (fr) 2018-12-28 2020-07-02 Cedars-Sinai Medical Center Méthodes de traitement de maladies intestinales inflammatoires ciblant la ripk2
WO2020146682A1 (fr) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Carboxamides utilisés en tant que modulateurs de canaux sodiques
US20220110923A1 (en) 2019-01-10 2022-04-14 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
JP7534306B2 (ja) 2019-01-22 2024-08-14 メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング 液晶ポリマーフィルムの製造方法
EP3917508A4 (fr) 2019-01-28 2022-12-21 Mitochondria Emotion, Inc. Activateurs de la mitofusine et leurs procédés d'utilisation
WO2020176763A1 (fr) 2019-02-27 2020-09-03 Vertex Pharmaceuticals Incorporated Forme posologique comprenant un promédicament inhibiteur de canal sodique na 1,8
WO2020190774A1 (fr) 2019-03-15 2020-09-24 The General Hospital Corporation Nouveaux inhibiteurs à petites molécules de facteurs de transcription tead
US12109179B2 (en) 2019-03-28 2024-10-08 Essa Pharma Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
WO2020219867A1 (fr) 2019-04-25 2020-10-29 Vertex Pharmaceuticals Incorporated Compositions de co-cristaux d'amide de pyridone pour le traitement de la douleur
EP3963026A1 (fr) 2019-04-30 2022-03-09 Merck Patent GmbH Mésogènes réactifs
US20220324880A1 (en) 2019-06-10 2022-10-13 Kymara Therapeutics, Inc. Smarca inhibitors and uses thereof

Also Published As

Publication number Publication date
US11603351B2 (en) 2023-03-14
US20190016671A1 (en) 2019-01-17
CL2020000075A1 (es) 2020-07-31
JP7277431B2 (ja) 2023-05-19
SG11202000230VA (en) 2020-02-27
DOP2020000004A (es) 2020-07-15
BR112020000553A2 (pt) 2020-07-21
TN2020000001A1 (en) 2021-10-04
KR20200026987A (ko) 2020-03-11
CR20200064A (es) 2020-08-03
JOP20200001A1 (ar) 2022-10-30
US20230286907A1 (en) 2023-09-14
IL271948A (en) 2020-02-27
US10647661B2 (en) 2020-05-12
AU2018300150A1 (en) 2020-01-30
UY37806A (es) 2020-01-31
CN111065383A (zh) 2020-04-24
WO2019014352A1 (fr) 2019-01-17
TW201920081A (zh) 2019-06-01
US20210094906A1 (en) 2021-04-01
PH12020500066A1 (en) 2020-09-28
JP2020526561A (ja) 2020-08-31
EP3651752A1 (fr) 2020-05-20
PE20201164A1 (es) 2020-10-28
ECSP20003147A (es) 2020-02-28
CO2020000145A2 (es) 2020-01-17
CA3069720A1 (fr) 2019-01-17

Similar Documents

Publication Publication Date Title
MA49566A (fr) Carboxamides utilisés en tant qu'inhibiteurs des canaux sodiques
MA52486A (fr) Pyridazinones utilisés en tant qu'inhibiteurs de parp7
MA51438A (fr) Composés hétérocycliques utilisés en tant qu'inhibiteurs de lsd1
MA48994A (fr) Isoquinoléines utilisées en tant qu'inhibiteurs de hpk1
MA43169A (fr) Composés hétérocycliques utilisés en tant qu'inhibiteurs de pi3k-gamma
MA47013A (fr) Composés benzolactames utilisés en tant qu'inhibiteurs de protéine kinase
MA51878A (fr) Composés d'aminothiazole en tant qu'inhibiteurs de c-kit
MA54076A (fr) 2-amino-n-hétéroaryl-nicotinamides utilisés en tant qu'inhibiteurs de nav1.8
MA54547A (fr) Amides d'hétéroaryle utiles en tant qu'inhibiteurs de kif18a
MA54546A (fr) Amides d'hétéroaryle utiles en tant qu'inhibiteurs de kif18a
MA40587A (fr) Composés d'aminopyrimidinyle en tant qu'inhibiteurs de jak
MA49903A (fr) Sulfonylureés et sulfonylthioureés en tant qu'inhibiteurs de nlrp3
MA42990A (fr) Composés utiles en tant qu'immunomodulateurs
MA43862A (fr) Spiroheptane salicylamides et composés associés en tant qu' inhibiteurs de rock
MA46196A (fr) Composés et compositions en tant qu'inhibiteurs de récepteurs de type toll endosomal
MA44725A (fr) Formulations d'un inhibiteur de lsd1
MA55194A (fr) Composés hétérocycliques en tant qu'immunomodulateurs
MA45244A (fr) Pyridines substituées utilisées en tant qu'inhibiteurs de dnmt1
MA46091A (fr) Composés biaryles utiles en tant qu'immunomodulateurs
MA42919A (fr) Composés bicycliques utilisés en tant qu'inhibiteurs d'atx
MA47460A (fr) Aminotriazolopyridines utilisées en tant qu'inhibiteurs de kinase
MA45377A (fr) Composés hétérocycliques en tant qu'agents antibacteriens
MA42918A (fr) Composés bicycliques utilisés en tant qu'inhibiteurs d'atx
MA41551A (fr) Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
MA54567A (fr) Pyridine et composés de pyridimine en tant qu'inhibiteurs de pi3k-gamma