AR058380A1 - Inhibidores del factor viia macrociclicos utiles como anticoagulantes - Google Patents
Inhibidores del factor viia macrociclicos utiles como anticoagulantesInfo
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- AR058380A1 AR058380A1 ARP060105501A ARP060105501A AR058380A1 AR 058380 A1 AR058380 A1 AR 058380A1 AR P060105501 A ARP060105501 A AR P060105501A AR P060105501 A ARP060105501 A AR P060105501A AR 058380 A1 AR058380 A1 AR 058380A1
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- substituted
- heterocycle
- nrcrd
- alkyl
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D245/00—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms
- C07D245/02—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms not condensed with other rings
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- C07—ORGANIC CHEMISTRY
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- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D245/00—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms
- C07D245/04—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D255/00—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00
- C07D255/02—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00 not condensed with other rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D255/00—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00
- C07D255/04—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00 condensed with carbocyclic rings or ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Peptides Or Proteins (AREA)
Abstract
Reivindicacion 1: Un compuesto caracterizado porque tiene la formula (1), o un estereoisomero, tautomero, sal farmacéuticamente aceptable, solvato, o forma de profármaco del mismo, en donde, el anillo A es fenilo o un isomero de piridilo definido al reemplazar uno de CR1, CR2, CR3, o CR4 en el anillo A de la formula (1) con N; el anillo B es fenilo o un isomero de piridilo definido al reemplazar uno de CR8, CR9, CR10, o CR11 en el anillo B de la formula (1) con N; para las definiciones de M y L, como se describen de izquierda a derecha, el átomo conectivamente esta en el orden (el anillo A)-L-M-(el anillo B); M es -CONH-, -SO2NH-, -NHCO-, o -NHSO2; cuando M es -CONH-, L se selecciona de -C(R12R13)C(R12R13)-, -XC(R12R13)-, -C(R12R13)Y-, - C(R12R13)C(R12R13)C(R12R13)-, -XC(R12R13)C(R12R13)-, -C(R12R13)XC(R12R13)-, -C(R12R13)C(R12R13)Y-, -XC(R12R13)Y-, -C(R12R13)C(R12R13)C(R12R13)C(R12R13)-, XC(R12R13)C(R12R13)C(R12R13)-, -C(R12R13)XC(R12R13)C(R12R13)-, -C(R12R13)C(R12R13)XC(R12R13)-, - C(R12R13)C(R12R13)C(R12R13)Y-, -XC(R12R13)C(R12R13)Y-, -XC(R12R13)XC(R12R13)-, y -C(R12R13)XC(R12R13)Y-; cuando M es -SO2NH-, L se selecciona de -C(R12R13)C(R12R13)-, -C(R12R13)C(R12R13)C(R12R13)-, -XC(R12R13)C(R12R13)-, - C(R12R13)C(R12R13)C(R12R13)C(R12R13)-, -XC(R12R13)C(R12R13)C(R12R13)-, -C(R12R13)XC(R12R13)C(R12R13)-, -C(R12R13)XC(R12R13)-, -C(R12R13)C(R12R13)Y-, -C(R12R13)C(R12R13)XC(R12R13)-, -C(R12R13)C(R12R13)C(R12R13)Y-, -XC(R12R13)C(R12R13)Y-, - XC(R12R13)XC(R12R13)-, -C(R12R13)XC(R12R13)Y-; cuando M es -NHCO-, L se selecciona de -C(R12R13)C(R12R13)-, -C(R12R13)C(R12R13)C(R12R13)-, -XC(R12R13)C(R12R13)-, -C(R12R13)C(R12R13)C(R12R13)-, -XC(R12R13)C(R12R13)C(R12R13)-, y - C(R12R13)XC(R12R13)C(R12R13)-; cuando M es -NHSO2-, L se selecciona de -C(R12R13)C(R12R13), -C(R12R13)C(R12R13)C(R12R13), -XC(R12R13)C(R12R13)-, -C(R12R13)C(R12R13)C(R12R13)C(R12R13)-, -XC(R12R13)C(R12R13)C(R12R13)-, y -C(R12R13)XC(R12R13)C(R12R13)- ; W es substituido con 0-2 R14 y se selecciona de un elemento del grupo de formulas (2); X es O, S(O)p, o NR16; Y es O o NR16a; Z es NH, O o S; R1 es H, F, CI, Br, I, alquilo C1-4 substituido con 0-1 OH, fluoroalquilo C1-4, alquenilo C2-4, alquinilo C2-4, alcoxi C1-4, alquiltio C1-4, o cicloalquilo C3-6; R2 es H, F, CI, Br, I, -(CH2)sORa, -(CH2)sSRb, -(CH2)sCF3, -(CH2)sOCF3, -(CH2)sOCHF2, -(CH2)sOCH2F, -(CH2)sCN, -(CH2)sNO2, -(CH2)sNRcRd, -(CH2)sC(O)Ra, -(CH2)sCO2Ra, -(CH2)sNRcC(O)Ra, - (CH2)sC(O)NRcRd, -(CH2)sNRcC(O)ORb, -(CH2)sOC(O)ORb, -(CH2)sNRcC(O)NRcRd, -(CH2)sOC(O)NRcRd, -(CH2)sSO2NRcRd, -(CH2)sNRcSO2NRcRd, -(CH2)sNRcSO2Rb, (CH2)sNRcSO2CF3, -(CH2)sSO2CF3, -(CH2)sS(O)2Rb, alquilo C1-6 substituido con 0-2 Re, fluoroalquilo C1- 4, alquenilo C2-4 substituido con 0-2 Re, alquinilo C2-4 substituido con 0-2 Re, -(CH2)s-carbociclo C3-6 substituido con 0-2 Rf, -(CH2)s-(heterociclo de 5 hasta 6 miembros), -(CH2)sNRc-(heterociclo de 5 hasta 6 miembros), o -(CH2)s-O-(heterociclo de 5 hasta 6 miembros); en donde el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0-2 Rg; R3 es H, F, CI, Br, I, -(CH2)sORa, -(CH2)sSRb, -(CH2)sCF3, -(CH2)sOCF3, -(CH2)sOCHF2, - (CH2)sOCH2F, -(CH2)sCN, -(CH2)sNO2, (CH2)sNRcRd, (CH2)sC(O)Ra, -(CH2)sCO2Ra, -(CH2)sNRcC(O)Ra, -(CH2)sC(O)NRcRd, -(CH2)sNRcC(O)ORb, -(CH2)sOC(O)ORb, -(CH2)sNRcC(O)NRcRd, (CH2)sOC(O)NRcRd, -(CH2)sSO2NRcRd, -(CH2)sNRcSO2NRcRd, -(CH2)sNRcSO2Rb, - (CH2)sNRcSO2CF3, -(CH2)sSO2CF3, -(CH2)sS(O)2Rb, -O(CH2)nCO2Ra, -(CH2)sSO2NHCORb, -(CH2)sCONHSO2Rb, alquilo C1-6 substituido con 0-2 Re, fluoroalquilo C1-4, alquenilo C2-4 substituido con 0-2 Re, alquinilo C2-4 substituido con 0-2 Re, -O(bencilo substituido con CO2Ra), -(CH2)stetrazolilo, -(CH2)scarbociclo C3-6 substituido con 0-2 Rf1, -(CH2)s-(heterociclo de 5 hasta 6 miembros), -(CH2)s-NRc-(heterociclo de 5 hasta 6 miembros), o -(CH2)s-O-(heterociclo de 5 hasta 6 miembros); en donde el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0-2 Rg1; alternativamente, R2 y R3 pueden combinarse para formar un carbociclo o heterociclo de 5 hasta 7 miembros que comprende: átomos de carbono y 0-2 heteroátomos seleccionados de N, NRc, O, y S(O)p; en donde el carbociclo y heterociclo están substituidos con 0-3 Rg1; R4 es H, F, CI, Br, I, o alquilo C1-4; R5 es H, -(CH2)qORa, -(CH2)qSRb, -(CH2)rCF3, -(CH2)qOCF3, - (CH2)qOCHF2, -(CH2)qOCH2F, -(CH2)qCN, -(CH2)qNO2, -(CH2)qNRcRd, -(CH2)sC(O)Ra, -(CH2)sCO2Ra, -(CH2)qNRcC(O)Ra, -(CH2)sC(O)NRcRd, -(CH2)qNRcC(O)ORb, -(CH2)qOC(O)ORb, -(CH2)qNRcC(O)NRcRd, -(CH2)qOC(O)NRcRd, -(CH2)qSO2NRcRd, -(CH2)qNRcSO2NRcRd, - (CH2)qNRcSO2Rb, -(CH2)qNRcSO2CF3, -(CH2)qSO2CF3, -(CH2)qS(O)2Rb, -(CH2)qSO2NHCORb, -(CH2)qCONHSO2Rb, -O(bencilo substituido con CO2Ra), -(CH2)stetrazolilo, alquilo C1-6 substituido con 0-2 Re, alquenilo C2-4 substituido con 0-2 Re, alquinilo C2-4 substituido con 0-2 Re, -(CH2)s-carbociclo C3-6 substituido con 0-2 Rf1, o heterociclo-(CH2)s- de 5 hasta 6 miembros; en donde el heterociclo comprende átomos de carbono y '1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0- 2 Rg1; R6 es H, -(CH2)rORa, -(CH2)rSRb, -(CH2)sCF3, -(CH2)rOCF3, -(CH2)rOCHF2, -(CH2)rOCH2F, -(CH2)sCN, -(CH2)sNO2, -(CH2)rNRcRd, -(CH2)sC(O)Ra, -(CH2)sCO2Ra, -(CH2)rNRcC(O)Ra, -(CH2)sC(O)NRcRd, -(CH2)rNRcC(O)ORb, -(CH2)rOC(O)ORb, - (CH2)rNRcC(O)NRcRd, -(CH2)rOC(O)NRcRd, -(CH2)rSO2NRcRd, -(CH2)rNRcSO2NRcRd, - (CH2)rNRcSO2Rb, -(CH2)rNRcSO2CF3, -(CH2)rSO2CF3, -(CH2)rS(O)2Rb, -(CH2)rSO2NHCORb, -(CH2)sCONHSO2Rb, alquilo C1-6 substituido con 0-2 Re, alquenilo C2-4 substituido con 0- 2 Re, alquinilo C2-4 substituido con 0-2 Re, -(CH2)s-carbociclo C3-6 substituido con 0-2 Rf1 o heterociclo-(CH2)s- de 5 hasta 6 miembros; en donde el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0-2 Rg1; alternativamente, R5 y R6 pueden unirse para formar una cadena alquileno de 2 hasta 5 miembros, la cual puede ser substituida con 0-1 Rf1; R7 es H o alquilo C1-6; alternativamente, R6 y R7 pueden unirse para formar un carbociclo o heterociclo de 3-7 miembros; en donde el carbociclo puede ser substituido con 0-2 Rf1; y el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0-2 Rg1; R8 es H, F, CI, Br, CN, CH2F, CHF2, -(CH2)sCF3, -(CH2)sOCF3, -(CH2)sSCF3, -(CH2)sOCHF2, -(CH2)sOCH2F, -(CH2)sCN, -(CH2)sNO2, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -(CH2)n-ORa, -(CH2)nSRb, -(CH2)nNRcRd, -(CH2)sC(O)Ra, -(CH2)sCO2Ra, -(CH2)sNRcC(O)Ra, - (CH2)sCONRcRd, -(CH2)sSO2Rb, -(CH2)sSO2NRcRd, -(CH2)sNRcC(O)ORb, -(CH2)sOC(O)ORb, -(CH2)sNRcC(O)NRcRd, -(CH2)sOC(O)NRcRd, -(CH2)sNRcSO2NRcRd, -(CH2)sNRcSO2Rb, -(CH2)sNRcSO2CF3, -(CH2)sSO2CF3, -O(CH2)nCO2Ra, -(CH2)sSO2NHCORb, -(CH2)sCONHSO2Rb, - O(bencilo substituido con CO2Ra), -(CH2)stetrazolilo, alquilo C1-6 substituido con 0-2 Re, fluoroalquilo C1-4, alquenilo C2-4 substituido con 0-2 Re, alquinilo C2-4 substituido con 0-2 Re, -(CH2)s-carbociclo C3-6 substituido con 0-2 Rf1, o heterociclo-(CH2)s- de 5 hasta 10 miembros que comprende: átomos de carbono y 1-4 heteroátomos seleccionados de N, NRc, O y S(O)p, en donde el fenilo y heterociclo están substituidos con 0-3 Rg1; R9, R10, y R11 son independientemente cada que se presentan H, E, CI, Br, I, alquilo C1-4, o alcoxi C1-4; R12 y R13 son independientemente cada que se presentan F, CI, ORa. SRb, CF3, OCF3, OCHF2, OCH2F, CN, NO2, .NRcRd, -C(O)Ra, -CO2Ra, NRcC(O)Ra, C(O)NRcRd, NRcC(O)ORb, -NRcC(O)NRcRd, OC(O)NRcRd, - OC(O)ORa, -SO2NRcRd, -NRcSO2NRcRd, -NRcSO2Rb, -NRcSO2CF3, -SO2CF3, -S(O)2Rb, alquilo C1-6 substituido con 0-2 Re, alquenilo C2-4 substituido con 0-2 Re, alquinilo C2-4 substituido con 0-2 Re, -(CH2)s-carbociclo C3-6 substituido con 0-2 Rf1, -(CH2)s- (heterociclo de 5 hasta 6 miembros), -NR-(heterociclo de 5 hasta 6 miembros)1 o -O-(heterociclo de 5 hasta 6 miembros); en donde el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0- 2 Rg1; alternativamente, cualquiera de dos R12 o R13 se enlazan ya sea al mismo carbono o a dos carbonos adyacentes pueden combinarse para formar un carbociclo o heterociclo de 3 hasta 7 miembros que comprende: átomos de carbono y 0-3 heteroátomos seleccionados de N, NRc, O, y S(O)p, en donde el carbociclo o heterociclo es substituido con 0-3 Rg; opcionalmente, dos R12 o R13 en átomos de carbono adyacentes en L pueden ser reemplazados con un enlace doble o triple entre los dos átomos de carbono; R14 es independientemente cada que se presenta CN, F, CI, Br, I, OH, N(R17R17), alquilo C1-3, o alcoxi C1-3; R15 es independientemente cada que se presenta H, -C(=NH)NH2, N(R17R17), -C(R17R17)N(R17R17), -CON(R17R17), CN, F, CI, Br, I, OH, alquilo C1-3, o alcoxi C1-3; R16 es independientemente cada que se presenta H, alquilo C1-4, cicloalquilo C3-6, fenilo, bencilo, -C(O)Ra, -C(O)NRcRd, -C(O)ORb, -SO2NRcRd, -SO2CF3, -S(O)2Rb, o -(CH2)s(heterociclo de 5 hasta 6 miembros); en donde el alquilo o cicloalquilo son opcionalmente substituidos con 0-2 Re, el fenilo y bencilo son opcionalmente substituidos con 0-2 Rf, y el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0-2 Rg; R16a es independientemente cada que se presenta H, alquilo C1-6, cicloalquilo C3-6, fenilo, bencilo, C(O)Ra, C(O)NRcRd, C(O)ORb, SO2NRcRd, -SO2CF3, S(O)2Rb, o heterociclo de 5 hasta 6 miembros; en donde el alquilo o cicloalquilo son opcionalmente substituidos con 0-2 Re, el fenilo y bencilo son opcionalmente substituidos con 0-2 Rf, y el heterociclo comprende átomos de carbono y 1-3 heteroátomos seleccionados de N, NRc, O, y S(O)p y es substituido con 0-2 Rg; R17 es independientemente cada que se presenta H o Me; Ra es independientemente cada que se presenta H, alquilo C1-4, cicloalquilo C3-6, fenilo, o bencilo; en donde el alquilo y cicloalquilo son opcion
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US75378605P | 2005-12-23 | 2005-12-23 | |
US86547506P | 2006-11-13 | 2006-11-13 |
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AR058380A1 true AR058380A1 (es) | 2008-01-30 |
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ARP060105501A AR058380A1 (es) | 2005-12-23 | 2006-12-13 | Inhibidores del factor viia macrociclicos utiles como anticoagulantes |
Country Status (16)
Country | Link |
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US (2) | US7592331B2 (es) |
EP (1) | EP1971582B1 (es) |
JP (1) | JP5139999B2 (es) |
KR (1) | KR20080087848A (es) |
AR (1) | AR058380A1 (es) |
AU (1) | AU2006330495A1 (es) |
BR (1) | BRPI0620254A2 (es) |
CA (1) | CA2634794A1 (es) |
EA (1) | EA200801592A1 (es) |
ES (1) | ES2395052T3 (es) |
IL (1) | IL192105A0 (es) |
NO (1) | NO20082629L (es) |
NZ (1) | NZ568715A (es) |
PE (1) | PE20071132A1 (es) |
TW (1) | TW200745062A (es) |
WO (1) | WO2007076431A1 (es) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PE20081775A1 (es) | 2006-12-20 | 2008-12-18 | Bristol Myers Squibb Co | Compuestos macrociclicos como inhibidores del factor viia |
EP2099783A1 (en) * | 2006-12-20 | 2009-09-16 | Brystol-Myers Squibb Company | Bicyclic lactam factor viia inhibitors useful as anticoagulants |
TW201311689A (zh) | 2011-08-05 | 2013-03-16 | 必治妥美雅史谷比公司 | 作為因子xia抑制劑之新穎巨環化合物 |
TW201319068A (zh) | 2011-08-05 | 2013-05-16 | 必治妥美雅史谷比公司 | 作為xia因子抑制劑之環狀p1接合劑 |
TWI586651B (zh) | 2011-10-14 | 2017-06-11 | 必治妥美雅史谷比公司 | 作為因子xia抑制劑之經取代四氫異喹啉化合物 |
EP2858977A1 (en) | 2012-06-08 | 2015-04-15 | Bristol-Myers Squibb Company | Macrocyclic factor viia inhibitors |
WO2014059214A1 (en) | 2012-10-12 | 2014-04-17 | Bristol-Myers Squibb Company | Guanidine and amine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
WO2014059203A1 (en) | 2012-10-12 | 2014-04-17 | Bristol-Myers Squibb Company | Crystalline forms of a factor xia inhibitor |
WO2014059202A1 (en) | 2012-10-12 | 2014-04-17 | Bristol-Myers Squibb Company | Guanidine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
US9738655B2 (en) | 2013-03-25 | 2017-08-22 | Bristol-Myers Squibb Company | Tetrahydroisoquinolines containing substituted azoles as factor XIa inhibitors |
EP3008052A1 (en) * | 2013-06-13 | 2016-04-20 | Bristol-Myers Squibb Company | Macrocyclic factor viia inhibitors |
NO2760821T3 (es) | 2014-01-31 | 2018-03-10 | ||
CN110845498B (zh) | 2014-01-31 | 2023-02-17 | 百时美施贵宝公司 | 作为因子xia抑制剂的具有杂环p2′基团的大环化合物 |
WO2016036893A1 (en) | 2014-09-04 | 2016-03-10 | Bristol-Myers Squibb Company | Diamide macrocycles that are fxia inhibitors |
US9453018B2 (en) | 2014-10-01 | 2016-09-27 | Bristol-Myers Squibb Company | Pyrimidinones as factor XIa inhibitors |
JP6742348B2 (ja) * | 2015-06-19 | 2020-08-19 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 第xia因子阻害剤としてのジアミド大員環 |
CN115404020B (zh) * | 2022-10-14 | 2023-06-30 | 深圳市高仁电子新材料有限公司 | 一种用于全贴合和柔性折叠屏的三层结构的丙烯酸类光学胶膜及其制备方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
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US5843442A (en) * | 1990-10-22 | 1998-12-01 | Corvas International, Inc. | Blood coagulation protein antagonists and uses therefor |
US5866542A (en) * | 1994-10-18 | 1999-02-02 | Corvas International, Inc. | Nematode-extracted anticoagulant protein |
WO1999013063A1 (en) * | 1997-09-09 | 1999-03-18 | Nycomed Imaging As | Factor vii fragments and analogs thereof and their use in the treatment of blood clottng disorders |
EP1332131A2 (en) * | 2000-11-07 | 2003-08-06 | Bristol-Myers Squibb Company | Acid derivatives useful as serine protease inhibitors |
AU2002322802A1 (en) | 2001-07-27 | 2003-02-17 | Merck And Co., Inc. | Thrombin inhibitors |
US7122559B2 (en) * | 2003-02-11 | 2006-10-17 | Bristol-Myers Squibb Company | Phenylglycine derivatives useful as serine protease inhibitors |
JP2006517589A (ja) * | 2003-02-11 | 2006-07-27 | ブリストル−マイヤーズ スクイブ カンパニー | セリンプロテアーゼ・インヒビターとして有用なベンゼンアセトアミド化合物 |
DE602006016566D1 (de) * | 2005-01-10 | 2010-10-14 | Bristol Myers Squibb Co | Als antikoagulanzien verwendbare phenylglycinamid-derivate |
US7456195B2 (en) * | 2005-06-24 | 2008-11-25 | Bristol-Myers Squibb Company | Phenylglycinamide and pyridylglycinamide derivatives useful as anticoagulants |
-
2006
- 2006-12-13 TW TW095146558A patent/TW200745062A/zh unknown
- 2006-12-13 AR ARP060105501A patent/AR058380A1/es unknown
- 2006-12-13 PE PE2006001599A patent/PE20071132A1/es not_active Application Discontinuation
- 2006-12-21 KR KR1020087017981A patent/KR20080087848A/ko not_active Application Discontinuation
- 2006-12-21 EP EP06846746A patent/EP1971582B1/en active Active
- 2006-12-21 US US11/614,131 patent/US7592331B2/en active Active
- 2006-12-21 JP JP2008547767A patent/JP5139999B2/ja not_active Expired - Fee Related
- 2006-12-21 AU AU2006330495A patent/AU2006330495A1/en not_active Abandoned
- 2006-12-21 BR BRPI0620254-3A patent/BRPI0620254A2/pt not_active IP Right Cessation
- 2006-12-21 CA CA002634794A patent/CA2634794A1/en not_active Abandoned
- 2006-12-21 EA EA200801592A patent/EA200801592A1/ru unknown
- 2006-12-21 WO PCT/US2006/062469 patent/WO2007076431A1/en active Application Filing
- 2006-12-21 NZ NZ568715A patent/NZ568715A/en not_active IP Right Cessation
- 2006-12-21 ES ES06846746T patent/ES2395052T3/es active Active
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2008
- 2008-06-04 NO NO20082629A patent/NO20082629L/no not_active Application Discontinuation
- 2008-06-12 IL IL192105A patent/IL192105A0/en unknown
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2009
- 2009-07-23 US US12/507,907 patent/US20090281139A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
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WO2007076431A1 (en) | 2007-07-05 |
AU2006330495A1 (en) | 2007-07-05 |
US20090281139A1 (en) | 2009-11-12 |
NO20082629L (no) | 2008-09-05 |
US7592331B2 (en) | 2009-09-22 |
BRPI0620254A2 (pt) | 2011-11-08 |
JP2009521505A (ja) | 2009-06-04 |
IL192105A0 (en) | 2008-12-29 |
EP1971582B1 (en) | 2012-10-10 |
PE20071132A1 (es) | 2007-12-14 |
JP5139999B2 (ja) | 2013-02-06 |
EA200801592A1 (ru) | 2008-12-30 |
US20070208054A1 (en) | 2007-09-06 |
KR20080087848A (ko) | 2008-10-01 |
CA2634794A1 (en) | 2007-07-05 |
EP1971582A1 (en) | 2008-09-24 |
TW200745062A (en) | 2007-12-16 |
ES2395052T3 (es) | 2013-02-07 |
NZ568715A (en) | 2011-01-28 |
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