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SG11201807021UA - Heteroaryl inhibitors of pad4 - Google Patents

Heteroaryl inhibitors of pad4

Info

Publication number
SG11201807021UA
SG11201807021UA SG11201807021UA SG11201807021UA SG11201807021UA SG 11201807021U A SG11201807021U A SG 11201807021UA SG 11201807021U A SG11201807021U A SG 11201807021UA SG 11201807021U A SG11201807021U A SG 11201807021UA SG 11201807021U A SG11201807021U A SG 11201807021UA
Authority
SG
Singapore
Prior art keywords
oxfordshire
abingdon
milton park
innovation
international
Prior art date
Application number
SG11201807021UA
Other languages
English (en)
Inventor
Rajesh Devraj
Gnanasambandam Kumaravel
Holly Atton
Edward Beaumont
Elise Gadouleau
Laura Gleave
Philip Stephen Kerry
Cristina Lecci
Mirco Meniconi
Nat Monck
Jordan Palfrey
Kostas Papadopoulos
Heather Tye
Philip A Woods
Original Assignee
Padlock Therapeutics Inc
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 Padlock Therapeutics Inc filed Critical Padlock Therapeutics Inc
Publication of SG11201807021UA publication Critical patent/SG11201807021UA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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SG11201807021UA 2016-02-23 2017-02-22 Heteroaryl inhibitors of pad4 SG11201807021UA (en)

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UY37134A (es) 2016-02-23 2017-08-31 Padlock Therapeutics Inc Compuestos heteroarilos y composiciones que los contienen útiles como inhibidores de pad4
ES2828623T3 (es) 2016-07-27 2021-05-27 Padlock Therapeutics Inc Inhibidores covalentes de PAD4
ES2924522T3 (es) 2016-09-12 2022-10-07 Padlock Therapeutics Inc Inhibidores heteroarilo de PAD4
WO2019059202A1 (ja) * 2017-09-19 2019-03-28 三菱瓦斯化学株式会社 半導体リソグラフィー膜形成組成物、並びにレジストパターン形成方法及びデバイス
WO2019058393A1 (en) * 2017-09-22 2019-03-28 Jubilant Biosys Limited HETEROCYCLIC COMPOUNDS AS INHIBITORS OF PAD
FI3697785T3 (fi) 2017-10-18 2023-04-03 Jubilant Epipad LLC Imidatsopyridiiniyhdisteitä pad:n estäjinä
US11629135B2 (en) 2017-11-06 2023-04-18 Jubilant Prodell Llc Pyrimidine derivatives as inhibitors of PD1/PD-L1 activation
WO2019102494A1 (en) 2017-11-24 2019-05-31 Jubilant Biosys Limited Heterocyclic compounds as prmt5 inhibitors
WO2019122202A1 (en) * 2017-12-20 2019-06-27 Ecole Polytechnique Federale De Lausanne (Epfl) Sting inhibitors
SG11202008950PA (en) 2018-03-13 2020-10-29 Jubilant Prodel LLC Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation
CN112566916B (zh) * 2018-08-08 2023-10-20 百时美施贵宝公司 作为pad4抑制剂的经取代的噻吩并吡咯
EP3833440A1 (en) 2018-08-08 2021-06-16 Bristol-Myers Squibb Company Indole and azaindole inhibitors of pad enzymes
ES2956090T3 (es) * 2018-08-08 2023-12-13 Bristol Myers Squibb Co Inhibidores de bencimidazol de enzimas PAD
CA3148490C (en) * 2019-08-30 2024-04-30 Jae Won Lee Imidazopyridine derivative and pharmaceutical composition comprising same as active ingredient
CN112574230B (zh) * 2019-09-27 2022-10-28 药捷安康(南京)科技股份有限公司 肽酰精氨酸脱亚胺酶抑制剂及其用途
JP2023509452A (ja) 2020-01-03 2023-03-08 バーグ エルエルシー がんを処置するためのube2kモジュレータとしての多環式アミド
CN113248507A (zh) * 2020-02-09 2021-08-13 上海茂晟康慧科技有限公司 瑞德西韦关键中间体7-卤代吡咯并[1,2-f][1,2,4]三嗪-4-胺的合成方法
WO2021222353A1 (en) 2020-04-30 2021-11-04 Gilead Sciences, Inc. Macrocyclic inhibitors of peptidylarginine deiminases
CN112618546B (zh) * 2020-12-22 2022-03-01 陈昊 Pad4抑制剂在制备放射治疗增敏药物方面的应用
US11878965B2 (en) 2020-12-22 2024-01-23 Gilead Sciences, Inc. Inhibitors of peptidylarginine deiminases
KR20220122879A (ko) * 2021-02-26 2022-09-05 주식회사 티에스디라이프사이언스 이미다조피리딘 유도체 및 이를 유효성분으로 함유하는 약학적 조성물

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CN104470919B (zh) 2012-07-26 2016-07-06 葛兰素集团有限公司 作为pad4抑制剂的2-(氮杂吲哚-2-基)苯并咪唑
CA2986199C (en) 2015-05-21 2023-07-18 Glaxosmithkline Intellectual Property Development Limited Benzoimidazole derivatives as pad4 inhibitors
AR107032A1 (es) * 2015-12-09 2018-03-14 Padlock Therapeutics Inc Inhibidores bicíclicos de pad4
AR107030A1 (es) 2015-12-09 2018-03-14 Padlock Therapeutics Inc Inhibidores aza-bencimidazol de pad4
UY37134A (es) 2016-02-23 2017-08-31 Padlock Therapeutics Inc Compuestos heteroarilos y composiciones que los contienen útiles como inhibidores de pad4
ES2828623T3 (es) * 2016-07-27 2021-05-27 Padlock Therapeutics Inc Inhibidores covalentes de PAD4
ES2924522T3 (es) 2016-09-12 2022-10-07 Padlock Therapeutics Inc Inhibidores heteroarilo de PAD4

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US20220081418A1 (en) 2022-03-17
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TW201825476A (zh) 2018-07-16
CN109071497B (zh) 2021-10-22
CA3015482A1 (en) 2017-08-31
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US11897866B2 (en) 2024-02-13
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KR20180110160A (ko) 2018-10-08
EA201891910A1 (ru) 2019-02-28
AR107694A1 (es) 2018-05-23
JP6926126B2 (ja) 2021-08-25
JP2019505597A (ja) 2019-02-28
UY37134A (es) 2017-08-31
WO2017147102A1 (en) 2017-08-31
MX2018009773A (es) 2018-11-29
BR112018016433A2 (pt) 2018-12-26
EP3419969B1 (en) 2019-12-18
EP3419969A1 (en) 2019-01-02
US11198681B2 (en) 2021-12-14

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