[go: up one dir, main page]

CL2016001076A1 - (aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolosis. - Google Patents

(aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolosis.

Info

Publication number
CL2016001076A1
CL2016001076A1 CL2016001076A CL2016001076A CL2016001076A1 CL 2016001076 A1 CL2016001076 A1 CL 2016001076A1 CL 2016001076 A CL2016001076 A CL 2016001076A CL 2016001076 A CL2016001076 A CL 2016001076A CL 2016001076 A1 CL2016001076 A1 CL 2016001076A1
Authority
CL
Chile
Prior art keywords
aza
inhibitors
pyridopyrazolopyrimidinones
indazolopyrimidinones
fibrinolosis
Prior art date
Application number
CL2016001076A
Other languages
English (en)
Inventor
Joachim Schuhmacher
Karl-Heinz Schlemmer
Jorma Hassfeld
Tom Kinzel
Johannes Kobberling
Kristin Beyer
Susanne Röhrig
Maria Köllnberger
Michael Sperzel
Nils Burkardt
Matthias Werner
Manuel Ellemann
Grande Yolanda Cancho
Christian Stegmann
Original Assignee
Bayer Pharma AG
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 Bayer Pharma AG filed Critical Bayer Pharma AG
Publication of CL2016001076A1 publication Critical patent/CL2016001076A1/es

Links

Classifications

    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D405/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D487/12Heterocyclic 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 three hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

COMPUESTOS DERIVADOS DE (AZA) PIRIDOPIRAZOLOPIRIMIDINONAS E INDAZOLOPIRIMIDINONAS, COMO INHIBIDORES DE FIBRINOLISIS; PROCESO PARA SU PREPARACION; COMPUESTOS INTERMEDIARIOS; MEDICAMENTO QUE LOS COMPRENDE, UTIL PARA EL TRATAMIENTO Y/O PROFILAXIS DE SANGRADO AGUDO Y RECURRENTE EN PACIENTES CON O SIN TRASTORNOS DE SANGRADO HEREDITARIOS O ADQUIRIDOS SUBYACENTES.
CL2016001076A 2013-11-05 2016-05-05 (aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolosis. CL2016001076A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP13191642 2013-11-05

Publications (1)

Publication Number Publication Date
CL2016001076A1 true CL2016001076A1 (es) 2016-12-09

Family

ID=49517406

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2016001076A CL2016001076A1 (es) 2013-11-05 2016-05-05 (aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolosis.

Country Status (28)

Country Link
US (3) US9598417B2 (es)
EP (1) EP3066100B1 (es)
JP (1) JP6431061B2 (es)
KR (1) KR102312780B1 (es)
CN (1) CN105683194B (es)
AP (1) AP2016009175A0 (es)
AR (1) AR098292A1 (es)
AU (1) AU2014345771B2 (es)
CA (1) CA2929378C (es)
CL (1) CL2016001076A1 (es)
CR (1) CR20160332A (es)
CU (1) CU24361B1 (es)
DO (1) DOP2016000102A (es)
EA (1) EA029373B1 (es)
ES (1) ES2732305T3 (es)
GT (1) GT201600084A (es)
IL (1) IL244645B (es)
MA (1) MA39018A1 (es)
MX (1) MX370419B (es)
PE (1) PE20160934A1 (es)
PH (1) PH12016500828A1 (es)
SG (1) SG11201602133RA (es)
TN (1) TN2016000161A1 (es)
TW (1) TWI657089B (es)
UA (1) UA117504C2 (es)
UY (1) UY35809A (es)
WO (1) WO2015067549A1 (es)
ZA (1) ZA201602311B (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UY35809A (es) * 2013-11-05 2015-05-29 Bayer Pharma AG (aza)piridopirazolopirimidinonas e indazolopirimidinonas y sus usos
MX2017005586A (es) * 2014-11-03 2017-06-19 Bayer Pharma AG Piperidinilpirazolopirimidinonas y utilización de las mismas.
WO2016173948A1 (en) * 2015-04-30 2016-11-03 Bayer Pharma Aktiengesellschaft Indazolopyrimidinones as fibrinolysis inhibitors
WO2017007917A1 (en) * 2015-07-07 2017-01-12 Mast Therapeutics, Inc. Polyoxyethylene/polyoxypropylene copolymers and fibrinolytic inhibitors, uses thereof and compositions
EP3318563A1 (en) 2016-11-07 2018-05-09 Sanofi Substituted pyrido[3,4-b]indoles for the treatment of cartilage disorders
CN110590673A (zh) * 2019-09-02 2019-12-20 南通大学 一种4-氯-7-甲基-1h-吲唑及其化学合成方法
US11618751B1 (en) 2022-03-25 2023-04-04 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 derivatives
US11654057B2 (en) 2020-04-09 2023-05-23 Bio 54, Llc Devices for bleeding reduction and methods of making and using the same
CN116848122B (zh) * 2021-02-05 2025-10-28 赛诺哈勃药业(成都)有限公司 一种纤溶酶抑制剂、其制备方法及应用
US11319319B1 (en) 2021-04-07 2022-05-03 Ventus Therapeutics U.S., Inc. Compounds for inhibiting NLRP3 and uses thereof
EP4352053A1 (en) 2021-06-09 2024-04-17 Eli Lilly and Company Substituted fused azines as kras g12d inhibitors
US11642324B1 (en) 2022-03-01 2023-05-09 Bio 54, Llc Topical tranexamic acid compositions and methods of use thereof
CN119278042A (zh) 2022-04-05 2025-01-07 索克普拉健康与人文科学公司 用于血栓性或血栓栓塞性病症中血栓的选择性溶解的糜蛋白酶抑制剂
US12331048B2 (en) 2022-10-31 2025-06-17 Ventus Therapeutics U.S., Inc. Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2192559A5 (en) * 1972-07-17 1974-02-08 Ugine Kuhlmann Pyrimidino (1,2-b) indazole derivs - inters for dyes and pharmaceuticals, from 3-aminoindazoles and beta-ketone derivs
WO2006023000A1 (en) 2004-07-30 2006-03-02 Xanodyne Pharmaceuticals, Inc. Tranexamic acid formulations
AR059224A1 (es) * 2006-01-31 2008-03-19 Jerini Ag Compuestos para la inhibicion de integrinas y uso de estas
RU2502736C2 (ru) * 2008-06-06 2013-12-27 Санофи-Авентис МАКРОЦИКЛИЧЕСКИЕ ПРОИЗВОДНЫЕ МОЧЕВИНЫ И СУЛЬФАМИДА В КАЧЕСТВЕ ИНГИБИТОРОВ TAFIa
WO2010114780A1 (en) 2009-04-01 2010-10-07 Merck Sharp & Dohme Corp. Inhibitors of akt activity
SG174463A1 (en) 2009-04-07 2011-10-28 Astrazeneca Ab Isoxazol-3(2h)-one analogs as therapeutic agents
WO2012047156A1 (en) * 2010-10-04 2012-04-12 Astrazeneca Ab Isoxazol-3(2h)-one analogs as plasminogen inhibitors and their use in the treatment of fibrinolysis related diseases
KR20140003438A (ko) * 2010-11-15 2014-01-09 카톨리에케 유니버시테이트 루벤 항바이러스성 축합 헤테로사이클릭 화합물
WO2012082947A1 (en) * 2010-12-16 2012-06-21 Irm Llc Compounds and compositions as tgr5 agonists
WO2012080237A1 (en) * 2010-12-16 2012-06-21 Bayer Pharma Aktiengesellschaft Substituted pyrimido[1,2-b]indazoles and their use as modulators of the pi3k/akt pathway
UY35809A (es) 2013-11-05 2015-05-29 Bayer Pharma AG (aza)piridopirazolopirimidinonas e indazolopirimidinonas y sus usos
WO2016173948A1 (en) * 2015-04-30 2016-11-03 Bayer Pharma Aktiengesellschaft Indazolopyrimidinones as fibrinolysis inhibitors

Also Published As

Publication number Publication date
PH12016500828A1 (en) 2016-06-13
WO2015067549A1 (en) 2015-05-14
AP2016009175A0 (en) 2016-04-30
JP2016535052A (ja) 2016-11-10
CU24361B1 (es) 2018-10-04
AR098292A1 (es) 2016-05-26
MA39018A1 (fr) 2017-06-30
IL244645A0 (en) 2016-04-21
HK1223940A1 (zh) 2017-08-11
AU2014345771A1 (en) 2016-04-14
UY35809A (es) 2015-05-29
NZ718100A (en) 2021-06-25
ES2732305T3 (es) 2019-11-21
EP3066100A1 (en) 2016-09-14
US10098883B2 (en) 2018-10-16
IL244645B (en) 2019-06-30
CN105683194A (zh) 2016-06-15
UA117504C2 (uk) 2018-08-10
CN105683194B (zh) 2018-09-14
JP6431061B2 (ja) 2018-11-28
US10668071B2 (en) 2020-06-02
EA201690935A1 (ru) 2016-10-31
MX2016005969A (es) 2016-08-11
US20180344739A1 (en) 2018-12-06
PE20160934A1 (es) 2016-10-08
AU2014345771B2 (en) 2018-09-13
US20170239251A1 (en) 2017-08-24
ZA201602311B (en) 2017-08-30
CA2929378A1 (en) 2015-05-14
EA029373B1 (ru) 2018-03-30
KR20160079093A (ko) 2016-07-05
CA2929378C (en) 2021-12-07
CR20160332A (es) 2016-11-10
TN2016000161A1 (en) 2017-10-06
EP3066100B1 (en) 2019-04-17
US20150126449A1 (en) 2015-05-07
MX370419B (es) 2019-12-11
GT201600084A (es) 2017-07-12
SG11201602133RA (en) 2016-05-30
TW201609728A (zh) 2016-03-16
DOP2016000102A (es) 2016-06-30
KR102312780B1 (ko) 2021-10-15
US9598417B2 (en) 2017-03-21
TWI657089B (zh) 2019-04-21

Similar Documents

Publication Publication Date Title
CL2016001076A1 (es) (aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolosis.
CY1124729T1 (el) Φαρμακοτεχνικες μορφες του ενζαλουταμιδιου
NI201600071A (es) Compuestos de inhibidor de autotaxina
MX378273B (es) Compuestos activos hacia bromodominios.
EA201890204A1 (ru) Антибактериальные соединения
CL2018000596A1 (es) Nuevos compuestos bicíclicos como inhibidores de la atx
MX2016004340A (es) Compuestos heterociclicos y usos de los mismos.
EA201990043A1 (ru) Антибактериальные соединения
MX2016002137A (es) Ciertas entidades quimicas, composiciones y metodos.
CL2016001082A1 (es) Proceso para la síntesis de un inhibidor de indolamina 2,3-dioxigenasa
MX384490B (es) Agentes que inducen apoptosis para el tratamiento de cancer y enfermedades inmunitarias y autoinmunitarias.
BR112015015891A8 (pt) Composição farmacêutica de solução sólida, e, uso de uma composição farmacêutica
EA201790575A1 (ru) Триазолопиразиноны в качестве ингибиторов pde1
BR112015017241A2 (pt) doadores de nitroxil com índice terapêutico melhorado
EA201792157A1 (ru) Имидазопиразиноны в качестве ингибиторов pde1
NI201600070A (es) Inhibidores tetracíclicos de autotaxina
ECSP16008797A (es) Derivados de heterobicicloaril como inhibidores rorc2 y métodos de uso de los mismos
MX382904B (es) Combinaciones de fármacos para tratar mieloma múltiple.
SV2017005412A (es) Compuestos de 1-alquil-6-oxo-1,6-dihidropiridin-3-ilo y usos de los mismos
CL2015002692A1 (es) Novedosos compuestos de bencenosulfonamida, método para sintetizarlos y uso de los compuestos en medicina y en cosméticos.
CL2016001210A1 (es) Análogos de bicalutamida o (s)- bicalutamida como compuestos activadores de la exocitosis para su uso en el tratamiento de un desorden de acúmulo lisosomal o glucogenosis.
BR112017024163A2 (pt) compostos bicíclicos
EA201691108A1 (ru) Хиназолин-thf-амины в качестве ингибиторов pde1
BR112016012248A2 (pt) método de tratamento de nefropatia
EA201691773A1 (ru) Галогенированные хиназолин-thf-амины в качестве ингибиторов pde1