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SG11201407228PA - N-aryltriazole compounds as lpar antagonists - Google Patents

N-aryltriazole compounds as lpar antagonists

Info

Publication number
SG11201407228PA
SG11201407228PA SG11201407228PA SG11201407228PA SG11201407228PA SG 11201407228P A SG11201407228P A SG 11201407228PA SG 11201407228P A SG11201407228P A SG 11201407228PA SG 11201407228P A SG11201407228P A SG 11201407228PA SG 11201407228P A SG11201407228P A SG 11201407228PA
Authority
SG
Singapore
Prior art keywords
international
new jersey
compounds
designated states
drive
Prior art date
Application number
SG11201407228PA
Other languages
English (en)
Inventor
Stephen Deems Gabriel
Matthew Michael Hamilton
Yimin Qian
Achyutharao Sidduri
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=48628669&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201407228P(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of SG11201407228PA publication Critical patent/SG11201407228PA/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
    • C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/14—Nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SG11201407228PA 2012-06-20 2013-06-17 N-aryltriazole compounds as lpar antagonists SG11201407228PA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261661953P 2012-06-20 2012-06-20
PCT/EP2013/062463 WO2013189865A1 (fr) 2012-06-20 2013-06-17 Composés n-aryltriazole utilisés comme antagonistes de lpar

Publications (1)

Publication Number Publication Date
SG11201407228PA true SG11201407228PA (en) 2014-12-30

Family

ID=48628669

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201407228PA SG11201407228PA (en) 2012-06-20 2013-06-17 N-aryltriazole compounds as lpar antagonists

Country Status (22)

Country Link
US (1) US20150133512A1 (fr)
EP (1) EP2864301A1 (fr)
JP (1) JP2015520203A (fr)
KR (1) KR20150011389A (fr)
CN (1) CN104395299A (fr)
AU (1) AU2013279513A1 (fr)
BR (1) BR112014030674A2 (fr)
CA (1) CA2869564A1 (fr)
CL (1) CL2014003241A1 (fr)
CO (1) CO7131357A2 (fr)
EA (1) EA201492281A1 (fr)
HK (1) HK1206339A1 (fr)
IL (1) IL236087A0 (fr)
IN (1) IN2014DN09352A (fr)
MA (1) MA37762B1 (fr)
MX (1) MX2014014711A (fr)
PE (1) PE20142305A1 (fr)
PH (1) PH12014502363A1 (fr)
SG (1) SG11201407228PA (fr)
UA (1) UA110310C2 (fr)
WO (1) WO2013189865A1 (fr)
ZA (1) ZA201408167B (fr)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014525932A (ja) 2011-08-15 2014-10-02 インターミューン， インコーポレイテッド リゾホスファチド酸レセプターアンタゴニスト
US20140213538A1 (en) * 2013-01-15 2014-07-31 Intermune, Inc. Lysophosphatidic acid receptor antagonists
WO2014145873A2 (fr) 2013-03-15 2014-09-18 Epigen Biosciences, Inc. Composés hétérocycliques utilisés pour le traitement de maladies
UY36060A (es) 2014-04-02 2015-10-30 Bayer Pharma AG Compuestos de azol sustituidos con amida
KR102433588B1 (ko) 2014-06-27 2022-08-19 우베 가부시키가이샤 할로겐 치환 헤테로환 화합물의 염
WO2017055316A1 (fr) 2015-10-01 2017-04-06 Bayer Pharma Aktiengesellschaft Composés azole à substitution amido
WO2017055313A1 (fr) 2015-10-01 2017-04-06 Bayer Pharma Aktiengesellschaft Composés azole amido-substitués
AR108838A1 (es) 2016-06-21 2018-10-03 Bristol Myers Squibb Co Ácidos de carbamoiloximetil triazol ciclohexilo como antagonistas de lpa
WO2018078005A1 (fr) 2016-10-29 2018-05-03 Bayer Pharma Aktiengesellschaft Dérivés d'azaspiro à substitution amido en tant qu'inhibiteurs de tankyrase
WO2018078009A1 (fr) 2016-10-29 2018-05-03 Bayer Pharma Aktiengesellschaft Dérivés de cyclohexane à substitution amido
WO2018087126A1 (fr) 2016-11-09 2018-05-17 Bayer Pharma Aktiengesellschaft Dérivés de cyclohexane à substitution amido en tant qu'inhibiteurs de tankyrase
CN107721984A (zh) * 2017-11-07 2018-02-23 大连理工大学 一种新型5‑酰胺基‑1,4,5‑三取代的1,2,3‑三氮唑的制备方法
CN107827829A (zh) * 2017-11-07 2018-03-23 大连理工大学 5‑酰胺基‑1,4,5‑三取代的1,2,3‑三氮唑在水相及生物介质中的制备方法
WO2019126099A1 (fr) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Acides carbamoyle cyclohexyliques à liaison n isoxazole utilisés en tant qu'antagonistes de lpa
BR112020012177A2 (pt) 2017-12-19 2020-11-24 Bristol-Myers Squibb Company azóis triazóis do ácido ciclo-hexílico como antagonistas de lpa
JP7202383B2 (ja) 2017-12-19 2023-01-11 ブリストル－マイヤーズ スクイブ カンパニー Ｌｐａアンタゴニストとしてのピラゾールｏ－架橋カルバモイルシクロヘキシル酸
CN112041316A (zh) 2017-12-19 2020-12-04 百时美施贵宝公司 作为lpa拮抗剂的异噁唑o-连接的氨基甲酰基环己基酸
ES2924704T3 (es) 2017-12-19 2022-10-10 Bristol Myers Squibb Co Pirazol azoles del ácido ciclohexílico como antagonistas de LPA
US11261180B2 (en) 2017-12-19 2022-03-01 Bristol-Myers Squibb Company Cyclohexyl acid isoxazole azoles as LPA antagonists
ES2944304T3 (es) 2017-12-19 2023-06-20 Bristol Myers Squibb Co Pirazol azinas de ácido ciclohexílico como antagonistas de LPA
WO2019126093A1 (fr) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Azines triazoles d'acide cyclohexyle utilisées en tant qu'antagonistes de lpa
EP3728209A1 (fr) 2017-12-19 2020-10-28 Bristol-Myers Squibb Company Azines isoxazole d'acide de cyclohexyle en tant qu'antagonistes de lpa
EA202091500A1 (ru) 2017-12-19 2020-09-14 Бристол-Маерс Сквибб Компани Пиразол n-связанные карбамоилциклогексильные кислоты в качестве антагонистов lpa
CN111434653A (zh) * 2019-01-15 2020-07-21 武汉朗来科技发展有限公司 三氮唑类化合物及其制备方法与用途
EP4058144A1 (fr) 2019-11-15 2022-09-21 Gilead Sciences, Inc. Pyridylsulfonamides de carbamate de triazole utilisées en tant qu'antagonistes du récepteur de lpa et leurs utilisations
CA3185689A1 (fr) 2020-06-03 2021-12-09 Gilead Sciences, Inc. Antagonistes du recepteur lpa et leurs utilisations
TWI843503B (zh) 2020-06-03 2024-05-21 美商基利科學股份有限公司 Lpa受體拮抗劑及其用途
TWI853704B (zh) 2021-05-11 2024-08-21 美商基利科學股份有限公司 Lpa受體拮抗劑及其用途
AU2022405082A1 (en) 2021-12-08 2024-07-11 Gilead Sciences, Inc. Lpa receptor antagonists and uses thereof
CN115745848A (zh) * 2022-12-07 2023-03-07 上海优合生物科技有限公司 一种氨基胍的加工合成工艺

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011159550A2 (fr) * 2010-06-14 2011-12-22 Amidra Pharmaceuticals, Inc. Antagoniste du récepteur de l'acide lysophosphatidique et ses utilisations
WO2011159633A1 (fr) * 2010-06-15 2011-12-22 Amira Pharmaceuticals, Inc. Formulations inhalables d'antagonistes de récepteur d'acide lysophosphatidique
KR20130126659A (ko) * 2010-12-07 2013-11-20 아미라 파마슈티칼스 인코포레이티드 리소포스파티드산 수용체 길항제 및 섬유증 치료에서의 그의 용도
WO2012138648A1 (fr) * 2011-04-06 2012-10-11 Irm Llc Compositions et procédés pour la modulation de récepteurs au lpa
JP2014525932A (ja) * 2011-08-15 2014-10-02 インターミューン， インコーポレイテッド リゾホスファチド酸レセプターアンタゴニスト
WO2013189864A1 (fr) * 2012-06-20 2013-12-27 F. Hoffmann-La Roche Ag Composés n-alkyltriazole utilisés comme antagonistes de lpar

Also Published As

Publication number Publication date
PE20142305A1 (es) 2015-01-16
MX2014014711A (es) 2015-03-04
KR20150011389A (ko) 2015-01-30
CN104395299A (zh) 2015-03-04
US20150133512A1 (en) 2015-05-14
BR112014030674A2 (pt) 2017-06-27
WO2013189865A1 (fr) 2013-12-27
EA201492281A1 (ru) 2015-04-30
CO7131357A2 (es) 2014-12-01
CA2869564A1 (fr) 2013-12-27
UA110310C2 (uk) 2015-12-10
IN2014DN09352A (fr) 2015-07-17
ZA201408167B (en) 2015-12-23
JP2015520203A (ja) 2015-07-16
AU2013279513A1 (en) 2014-10-16
CL2014003241A1 (es) 2015-03-20
MA37762A1 (fr) 2017-07-31
MA37762B1 (fr) 2018-04-30
HK1206339A1 (en) 2016-01-08
PH12014502363A1 (en) 2015-01-12
IL236087A0 (en) 2015-02-01
EP2864301A1 (fr) 2015-04-29

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