ZA201407799B - Imidazothiadiazole an imidazopyrazine derivatives as protease activated receptor 2(par4) inhibitors for treating platelet aggregation - Google Patents

Imidazothiadiazole an imidazopyrazine derivatives as protease activated receptor 2(par4) inhibitors for treating platelet aggregation

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Publication number
ZA201407799B
ZA201407799B ZA2014/07799A ZA201407799A ZA201407799B ZA 201407799 B ZA201407799 B ZA 201407799B ZA 2014/07799 A ZA2014/07799 A ZA 2014/07799A ZA 201407799 A ZA201407799 A ZA 201407799A ZA 201407799 B ZA201407799 B ZA 201407799B
Authority
ZA
South Africa
Prior art keywords
imidazothiadiazole
par4
inhibitors
platelet aggregation
activated receptor
Prior art date
Application number
ZA2014/07799A
Other languages
English (en)
Inventor
Michael R Lawrence
Brad D Maxwell
Eldon Scott Priestley
Laurence Dube
Daniel H Deon
Roger Remillard
Michael M Miller
Pancras C Wong
Shoshana L Posy
Julia Guy
Marc Gagnon
Edward H Ruediger
Jacques Banville
Original Assignee
Bristol Myers Squibb Co
Univ Montreal
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 Bristol Myers Squibb Co, Univ Montreal filed Critical Bristol Myers Squibb Co
Publication of ZA201407799B publication Critical patent/ZA201407799B/en

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    • C07ORGANIC CHEMISTRY
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    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
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    • 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
    • A61K31/433Thidiazoles
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    • 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
    • A61K31/4355Heterocyclic 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 oxygen as a ring hetero atom
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/4965Non-condensed pyrazines
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    • A61K31/50Pyridazines; Hydrogenated pyridazines
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53861,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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  • Nitrogen Condensed Heterocyclic Rings (AREA)
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ZA2014/07799A 2012-04-26 2014-10-24 Imidazothiadiazole an imidazopyrazine derivatives as protease activated receptor 2(par4) inhibitors for treating platelet aggregation ZA201407799B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261638577P 2012-04-26 2012-04-26
US201361787680P 2013-03-15 2013-03-15
PCT/US2013/037956 WO2013163279A1 (en) 2012-04-26 2013-04-24 Imidazothiadiazole and imidazopyrazine derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation

Publications (1)

Publication Number Publication Date
ZA201407799B true ZA201407799B (en) 2015-12-23

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ZA2014/07799A ZA201407799B (en) 2012-04-26 2014-10-24 Imidazothiadiazole an imidazopyrazine derivatives as protease activated receptor 2(par4) inhibitors for treating platelet aggregation

Country Status (36)

Country Link
US (6) US9688695B2 (en:Method)
EP (3) EP3632919B1 (en:Method)
JP (1) JP6073464B2 (en:Method)
KR (3) KR102176379B1 (en:Method)
CN (2) CN104583218B (en:Method)
AR (1) AR090834A1 (en:Method)
AU (1) AU2013251632B2 (en:Method)
BR (1) BR112014026643B1 (en:Method)
CA (1) CA2871650C (en:Method)
CL (1) CL2014002915A1 (en:Method)
CO (1) CO7160040A2 (en:Method)
CY (2) CY1119466T1 (en:Method)
DK (3) DK3632919T3 (en:Method)
EA (1) EA026724B1 (en:Method)
ES (3) ES2935173T3 (en:Method)
FI (1) FI3632919T3 (en:Method)
HR (3) HRP20171453T1 (en:Method)
HU (3) HUE060743T2 (en:Method)
IL (1) IL235246B (en:Method)
LT (2) LT2841437T (en:Method)
MX (1) MX354175B (en:Method)
MY (1) MY175061A (en:Method)
NZ (1) NZ631027A (en:Method)
PE (1) PE20142285A1 (en:Method)
PH (1) PH12014502173B1 (en:Method)
PL (3) PL3243826T3 (en:Method)
PT (3) PT3243826T (en:Method)
RS (3) RS56395B1 (en:Method)
SG (1) SG11201406757SA (en:Method)
SI (3) SI3243826T1 (en:Method)
SM (3) SMT202300004T1 (en:Method)
TN (1) TN2014000436A1 (en:Method)
TW (1) TWI572605B (en:Method)
UY (1) UY34763A (en:Method)
WO (1) WO2013163279A1 (en:Method)
ZA (1) ZA201407799B (en:Method)

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WO2013163244A1 (en) 2012-04-26 2013-10-31 Bristol-Myers Squibb Company Imidazothiadiazole derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation
JP6101343B2 (ja) 2012-04-26 2017-03-22 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 血小板凝集を治療するためのプロテアーゼ活性化受容体4(par4)阻害剤としてのイミダゾチアジアゾールおよびイミダゾピリダジン誘導体
LT2841437T (lt) 2012-04-26 2017-09-11 Bristol-Myers Squibb Company Imidazotiadiazolo ir imidazopirazino dariniai, kaip proteazės aktyvuotų receptorių 4 (par4) inhibitoriai, skirti trombocitų agregacijos gydymui
TWI568722B (zh) 2012-06-15 2017-02-01 葛蘭馬克製藥公司 作爲mPGES-1抑制劑之三唑酮化合物
ES2649156T3 (es) 2013-01-14 2018-01-10 Incyte Holdings Corporation Compuestos bicíclicos de carboxamida aromática útiles como inhibidores de quinasas Pim
EA035929B1 (ru) 2013-01-15 2020-09-02 Инсайт Холдингс Корпорейшн ТИАЗОЛКАРБОКСАМИДЫ И ПИРИДИНКАРБОКСАМИДЫ, ИСПОЛЬЗУЕМЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ Pim-КИНАЗЫ
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ES2929208T3 (es) 2015-02-26 2022-11-25 Univ Montreal Compuestos de imidazotiadiazol como inhibidores de PAR4
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US9789087B2 (en) 2015-08-03 2017-10-17 Thomas Jefferson University PAR4 inhibitor therapy for patients with PAR4 polymorphism
AR105967A1 (es) 2015-09-09 2017-11-29 Incyte Corp Sales de un inhibidor de pim quinasa
TW201718546A (zh) 2015-10-02 2017-06-01 英塞特公司 適用作pim激酶抑制劑之雜環化合物
WO2017066863A1 (en) 2015-10-19 2017-04-27 Universite De Montreal Heterocyclic compounds as inhibitors of platelet aggregation
US9963466B2 (en) 2016-03-07 2018-05-08 Vanderbilt University Substituted 5-membered heterocyclic analogs as protease activated receptor 4 (PAR-4) antagonists
US20190119300A1 (en) * 2016-04-18 2019-04-25 Vanderbilt University Substituted and fused 6-membered protease activated receptor 4 (par-4) antagonists
KR102460385B1 (ko) * 2016-07-14 2022-10-27 브리스톨-마이어스 스큅 컴퍼니 비시클릭 헤테로아릴 치환된 화합물
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