AR058400A1 - Derivados de oxazoloisoquinolina como antagonistas del receptor de trombina - Google Patents
Derivados de oxazoloisoquinolina como antagonistas del receptor de trombinaInfo
- Publication number
- AR058400A1 AR058400A1 ARP060105664A ARP060105664A AR058400A1 AR 058400 A1 AR058400 A1 AR 058400A1 AR P060105664 A ARP060105664 A AR P060105664A AR P060105664 A ARP060105664 A AR P060105664A AR 058400 A1 AR058400 A1 AR 058400A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- independently selected
- hydrogen
- substituted
- Prior art date
Links
- BNZWLTVMPQNISM-UHFFFAOYSA-N [1,3]oxazolo[4,5-h]isoquinoline Chemical class C1=CN=CC2=C(OC=N3)C3=CC=C21 BNZWLTVMPQNISM-UHFFFAOYSA-N 0.000 title abstract 2
- 102000003790 Thrombin receptors Human genes 0.000 title 1
- 108090000166 Thrombin receptors Proteins 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 34
- 229910052739 hydrogen Inorganic materials 0.000 abstract 18
- 239000001257 hydrogen Substances 0.000 abstract 18
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 17
- 125000003545 alkoxy group Chemical group 0.000 abstract 13
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 11
- 150000002367 halogens Chemical class 0.000 abstract 11
- -1 -OH Chemical group 0.000 abstract 7
- 125000004429 atom Chemical group 0.000 abstract 7
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 6
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000004104 aryloxy group Chemical group 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 150000001721 carbon Chemical group 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- SGAAGTUHTZAXEI-UHFFFAOYSA-N 1,2,4-trioxolan-3-one Chemical group C1OC(=O)OO1 SGAAGTUHTZAXEI-UHFFFAOYSA-N 0.000 abstract 1
- 125000006345 2,2,2-trifluoroethoxymethyl group Chemical group [H]C([H])(*)OC([H])([H])C(F)(F)F 0.000 abstract 1
- 206010002383 Angina Pectoris Diseases 0.000 abstract 1
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- 206010019280 Heart failures Diseases 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 208000007536 Thrombosis Diseases 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical group 0.000 abstract 1
- 150000001412 amines Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical group [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 206010003119 arrhythmia Diseases 0.000 abstract 1
- 230000006793 arrhythmia Effects 0.000 abstract 1
- 125000005127 aryl alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 239000004202 carbamide Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000003857 carboxamides Chemical group 0.000 abstract 1
- 229940125692 cardiovascular agent Drugs 0.000 abstract 1
- 239000002327 cardiovascular agent Substances 0.000 abstract 1
- 238000002648 combination therapy Methods 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000004980 cyclopropylene group Chemical group 0.000 abstract 1
- 125000004982 dihaloalkyl group Chemical group 0.000 abstract 1
- 125000004990 dihydroxyalkyl group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 201000010235 heart cancer Diseases 0.000 abstract 1
- 208000024348 heart neoplasm Diseases 0.000 abstract 1
- 125000005326 heteroaryloxy alkyl group Chemical group 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 abstract 1
- 208000037803 restenosis Diseases 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 102200012954 rs121918642 Human genes 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000005415 substituted alkoxy group Chemical group 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- 150000003456 sulfonamides Chemical group 0.000 abstract 1
- IMCGHZIGRANKHV-AJNGGQMLSA-N tert-butyl (3s,5s)-2-oxo-5-[(2s,4s)-5-oxo-4-propan-2-yloxolan-2-yl]-3-propan-2-ylpyrrolidine-1-carboxylate Chemical compound O1C(=O)[C@H](C(C)C)C[C@H]1[C@H]1N(C(=O)OC(C)(C)C)C(=O)[C@H](C(C)C)C1 IMCGHZIGRANKHV-AJNGGQMLSA-N 0.000 abstract 1
- 125000004385 trihaloalkyl group Chemical group 0.000 abstract 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/42—Oxazoles
- A61K31/424—Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
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Abstract
Se describen derivados de oxazoloisoquinolina, así como también composiciones farmacéuticas que contienen a los mismos y un método para tratar enfermedades asociadas con trombosis, ateroesclerosis, restenosis, hipertension, angina de pecho, arritmia, insuficiencia cardiaca, y cáncer administrando dichos compuestos. También se reivindica una terapia de combinacion con otros agentes cardiovasculares. Reivindicacion 1: Un compuesto representado por la formula (1), o una sal, solvato, o éster farmacéuticamente aceptable de dicho compuesto, donde la línea punteada representa un enlace doble o simple, segun lo permitido por el requerimiento de valencia; con la condicion de que R10 o R11 están ausentes cuando el carbono al cual R10 o R11 están unidos es parte de un enlace doble; B es -(CH2)n3-, -(CH2)-O-, -(CH2)S-, -(CH2)-NR6-, -C(O)NR6-. -NR6C(O)-, ciclopropileno, -(CH2)n4CR12=CR12a(CH2)n5 o -(CH2)n4CsC(CH2)n5- donde n3 es 0-5, n4 y n5 son independientemente 0-2, y R12 y R12a se seleccionan independientemente entre el grupo que consiste en hidrogeno, alquilo C1-6 y halogeno; A, G, J, M y U se seleccionan independientemente del grupo formado por -N(R54)-, -(CR1R2)-, -O-, >C=O, -S-, -S(O)-, -S(O)2- Y >N=R1; con la condicion de que la seleccion de A, G, U, J, y M no de como resultado átomos de oxígeno o de azufre adyacentes y que al menos un átomo de carbono aparezca entre cualquier átomo de oxígeno, nitrogeno o azufre; cada n es independientemente 0, 1 o 2 con la condicion de que todas las variables n no pueden ser simultáneamente 0 y que el total de variables n no puede ser mayor que 7; K se selecciona del grupo formado por , >C=, -CR1-, y -N-; Het es un grupo mono-, bi- o tricíclico heteroaromático de 5 a 14 átomos compuesto por 1 a 13 átomos de carbono y de 1 a 4 heteroátomos seleccionados independientemente del grupo formado por N, O y S, con la condicion de que no haya átomos de oxigeno o de azufre adyacentes presentes en el grupo heteroaromático, donde un nitrogeno en el anillo puede formar un N-oxido o grupo cuaternario con un grupo alquilo, donde Het está unido a B mediante un miembro del anillo del átomo de carbono, y donde el grupo Het es sustituido por 1 a 4 porciones, W, donde cada W se selecciona independientemente del grupo formado por hidrogeno, alquilo, fluoralquilo, difluoralquilo, trifluoralquilo, haloalquilo, dihaloalquilo, trihaloalquilo, cicloalquilo, cicloalquilo sustituido con alquilo, alquenilo, o alquinilo, heterocicloalquilo, heterocicloalquilo sustituido con alquilo, alquenilo, o alquinilo, R21-arilalquilo, R21-aril-alquenilo, heteroarilo, heteroarilalquilo, heteroarilalquenilo, hidroxialquilo, dihidroxialquilo, aminoalquilo, alquilaminoalquilo, di-(alquil)-aminoalquilo, tioalquilo, alcoxi, alqueniloxi, halogeno, -NR4R5, -SH, -CN, -OH, -C(O)OR17, -COR16, -OS(O2)CF3, -CH2OCH2CF3, alquiltio, -C(O)NR4R5, -OCHR6-fenilo, fenoxialquilo, -NHCOR16, -NHSO2R16, bifenilo, - OC(R6)2COOR7, -OC(R6)2C(O)NR4R5, alcoxi sustituido con alquilo, amino o -NHC(O)OR17, arilo, arilo sustituido con 1 a 3 sustituyentes seleccionados independientemente del grupo formado por alquilo, halogeno, alcoxi, metilendioxi, ácido carboxílico, carboxamida, amina, urea, amida, sulfonamida, -CN, -CF3, -OCF3, -OH, alquilamino-, di-(alquil)amino-, -NR25R26-alquil-, hidroxialquil-, -C(O)OR17, -COR17, -NHCOR16, -NHS(O)2R16, -NHS(O)2CH2CF3, -C(O)NR25R26, NR25-C(O)-NR25R26, -S(O)R13, -S(O)2R13 y - SR13, o alquilo opcionalmente sustituido con -NR1R2, -NR1COR2, -NR1CONR1R2, -NR1C(O)OR2, -NR1S(O)2R2, -NR1S(O)2NR1R2, -C(O)OH, -C(O)OR1, -CONR1R2-heteroarilo, hidroxialquilo, alquilo, -S(O)2-alquilo, -C(O)NR4R5 o heteroarilo; donde carbonos adyacentes en el anillo Het pueden formar opcionalmente un anillo con un grupo metilendioxi; R1 y R2 se seleccionan independientemente del grupo formado por hidrogeno, halogeno, alquilo, fluoralquilo, difluoralquilo, trifluoralquilo, cicloalquilo, alquenilo, alcoxi, arilalquilo, arilalquenilo, heteroarilalquilo, heteroarilalquenilo, hidroxi, hidroxialquilo, alcoxialquilo, amina, aminoalquilo, arilo, tiohidroxi, CN, y tioalquilo; o R1 y R2 cuando se unen a nitrogeno, tomados en forma conjunta, forman un anillo mono o bicíclico heterocíclico de 4 a 10 átomos, con 1-3 heteroátomos seleccionados entre -O-, -N-, -S-, -S(O)-, -S(O)2- y >C=O, con la condicion de que átomos del anillo S y O no están adyacentes entre sí, donde dicho anillo heterocíclico está no sustituido o sustituido con uno o más grupos seleccionados independientemente entre alquilo, halogeno, hidroxi, alcoxi, ariloxi y arilalcoxi; R6 es hidrogeno, alquilo o fenilo; R7 es hidrogeno o alquilo; R16 y R16a se seleccionan independientemente del grupo formado por hidrogeno, alquilo, fenilo y bencilo; R16b es hidrogeno, alcoxi, alquilo, alcoxialquilo-, R22-O-C(O)-alquil-, cicloalquilo, R21-arilo, R21-arilalquilo, haloalquilo, alquenilo, alquenilo halo sustituido, alquinilo, alquinilo halo sustituido, R21-heteroarilo, (R21-heteroaril)-alquil-, (R21-heterocicloalquil)-alquil-, R28R29N-alquil-, R28R29N-C(O)-alquil-, R28R29N-C(O)O-alquil-, R28OC(O)N(R29)-alquil-, R28S(O)2N(R29)-alquil-, R28R29N-C(O)- N(R29)-alquil-, R28R29N-S(O)2N(R29)-alquil-, R28-C(O)N(R29)-alquil-, R28R29N-S(O)2-alquil-, HOS(O)2-alquil-, (OH)2P(O)2-alquil-, R28-S-alquil-, R28-S(O)2-alquil-, o hidroxialquilo; R17 se selecciona del grupo formado por hidrogeno, alquilo, fenilo y bencilo; R18 y R19 son hidrogeno, alquilo, arilo, R21-arilo, heteroarilo, cicloalquilo, heterociclilo, alcoxialquilo, haloalcoxialquilo, ariloxialquilo, arilalcoxialquilo, heteroariloxialquilo, (heterociclil)alquiloxialquilo, alcoxialquiloxialquilo, -S(O)2-alquilo, -C(NH)NR1R2 o alquilo sustituido con una o dos porciones seleccionadas independientemente del grupo formado por cicloalquilo, halogeno, hidroxi, -NR1R2, -NR1C(O)R2, -NR1C(O)NR1R2, -NR1C(O)OR2, NR1S(O)2R2, -NR1S(O)2NR1R2, -C(O)OH, - C(O)OR1 y -C(O)NR1R2; o R18 y R19 junto con el nitrogeno al cual están unidos, forman un anillo heterocíclico mono o bicíclico de 4 a 10 átomos, con 1-3 heteroátomos en el anillo seleccionados del grupo formado por -O-, -N-, -S-, -S(O)-, -S(O)2-. y >C=O, con la condicion de que los átomos de S y O no sean adyacentes entre sí, estando el anillo no sustituido o sustituido con uno o más grupos seleccionados independientemente entre alquilo, halogeno, hidroxi, alcoxi, ariloxi, arilalcoxi, -NR1R2, - NR1COR2, -NR1C(O)NR1R2, -NR1C(O)OR2, -NR1S(O)2R2, -NR1S(O2)NR1R2, -C(O)OR1, -CONR1R2 y alquilo sustituido con -NR1R2, -NR1COR2, -NR1CONR1R2, -NR1C(O)OR2, -NR1S(O)2R2, -NR1S(O)2NR1R2, -C(O)OR1 o -CONR1R2; R21 es 1 a 3 porciones y cada R21 se selecciona independientemente del grupo formado por hidrogeno, -CN, -CF3, -OCF3, halogeno, -NO2, alquilo, -OH, alcoxi, alquilamino-, di-(alquil)amino-, -NR25R26-alquil-, hidroxialquil-, -C(O)OR17, -COR17, -NHCOR16, -NHS(O)2R16, -C(NH)-NH2, - NHS(O)2CH2CF3, -C(O)NR25R26, -NR25-C(O)-NR25R26, -S(O)R16, -S(O)2R16, -SR16, -SO2NR4R5 y -CONR4R5; o dos porciones R21 adyacentes pueden formar un grupo metilendioxi; R22 es hidrogeno, alquilo, fenilo, bencilo, -COR16, CONR18R19, -COR23, -S(O)R31, - S(O)2R31, -S(O2)NR24R25 o -C(O)OR27; R23 es -C(NH2)R35R36, donde R35 y R36 se seleccionan independientemente del grupo formado por hidrogeno, alquilo, y R37-alquilo sustituido, donde R37 se selecciona del grupo formado por HO-, HS-, CH2S-,-NH2, fenilo, p-hidroxifenilo e indolilo; o R23 es alquilo, haloalquilo, alquenilo, haloalquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquilo sustituido con 1 a 3 sustituyentes seleccionados independientemente del grupo formado por alcoxialquilo, alquilo, halogeno, hidroxi, alcoxi, ariloxi, arilalcoxi, -NR1R2, -NR1C(O)R2, -NR1C(O)NR1R2, -NR1C(O)OR2, -NR1S(O)2R2, -NR1S(O)2NR1R2, -C(O)OH, -C(O)OR1 y -CONR1R2, arilo, aralquilo, heteroarilo, heterocicloalquilo, o alquilo sustituido con -NR1R2, -NR1COR2, -NR1CONR1R2, -NR1C(O)OR2, -NR1S(O2)R2, -NR1S(O2)NR1R2, -C(O)OH, -C(O)OR1, -CONR1R2 o -SO3H; R24, R25 y R26 se seleccionan independientemente del grupo formado por hidrogeno, alquilo, haloalquilo, alquenilo, alquinilo, arilo, aralquilo, cicloalquilo, halocicloalquilo, alcoxialquilo, hidroxi y alcoxi; R27 es 1 a 3 porciones y cada R27 se selecciona independientemente del grupo formado por hidrogeno, alquilo, y cicloalquilo, donde cuando R27 es alquilo o cicloalquilo, R27 es opcionalmente sustituido con -OH, -C(O)OH, halogeno o alcoxi; R28 y R29 se seleccionan independientemente del grupo formado por hidrogeno, alquilo, alcoxi, arilalquilo, heteroarilo, heteroarilalquilo, hidroxialquilo, alcoxialquilo, heterociclilo, heterociclilalquilo, y haloalquilo; o R28 y R29 tomados en conjunto forman un anillo espirocíclico o un anillo heteroespirocíclico que tiene de 3-6 átomos en el anillo; R32 y R33 se seleccionan independientemente del grupo formado por hidrogeno, R34-alquilo, R34-alquenilo, R34-alquinilo, R40-heterocicloalquilo, R38-arilo, R38-aralquilo, R42-cicloalquilo, R42-cicloalquenilo, -OH, -OC(O)R43, -C(O)OR43, -C(O)R43, -C(O)NR43R44, -NR43R44, -NR43C(O)R44, - NR43C(O)NR44R45, -NHS(O)2R43, -OC(O)NR43R44, R37-alcoxi, R37-alqueniloxi, R37-alquiniloxi, R40-heterocicloalquiloxi, R42-cicloalquiloxi, R42-ciclo-alqueniloxi, R42-cicloalquil-NH-, -NHSO2NHR16 y -CH(=NOR17); o R32 y R10 junto con el carbono al cual están unidos, o R33 y R11 junto con el carbono al cual están unidos, forman independientemente un anillo carbocíclico R42-sustituido de 3-10 átomos; o un anillo heterocíclico R42-sustituido de 4-10 átomos donde 1-3 miembros del anillo se seleccionan independientemente del grupo formado por -O-, -NH- y -SO0-2-, siempre y cuando R32 y R10 formen un anillo, o R33 y R11 formen un anillo el enlace doble opcional está ausente; R42 es 1 a 3 sustituyentes seleccionados independientemente del grupo formado por hidrogeno, -OH, alquilo C1-6, alcoxi C1-6, NH2, y halogeno; o R32 y R33 se combinan para formar una estructura de anillo Q representada por la formula (2), donde R9 es hidrogen
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| TW201100398A (en) * | 2009-03-31 | 2011-01-01 | Arqule Inc | Substituted indolo-pyridinone compounds |
| EP2558465B1 (de) | 2010-04-16 | 2014-12-17 | Sanofi | Trizyklische pyridyl-vinyl-pyrrole als par1-inhibitoren |
| ES2527535T3 (es) | 2010-04-16 | 2015-01-26 | Sanofi | Piridil-vinil-pirazolo-quinolinas como inhibidores de PAR1 |
| JO3210B1 (ar) | 2011-10-28 | 2018-03-08 | Merck Sharp & Dohme | مثبط منصهر لبروتين نقل الكوليسترليستير اوكسازوليدينون ثمائي الحلقة |
| US9340530B2 (en) | 2012-03-06 | 2016-05-17 | Merck Sharp & Dohme Corp. | Preparation and use of bicyclic himbacine derivatives as PAR-1 receptor antagonists |
| US9701669B2 (en) | 2013-08-22 | 2017-07-11 | Merck Sharp & Dohme Corp. | Preparation and use of 7a-amide substituted- 6,6-difluoro bicyclic himbacine derivatives as PAR-1 receptor antagonists |
| WO2015026685A1 (en) | 2013-08-22 | 2015-02-26 | Merck Sharp & Dohme Corp. | 7a-heterocycle substituted- 6, 6-difluoro bicyclic himbacine derivatives |
| WO2015026686A1 (en) * | 2013-08-22 | 2015-02-26 | Merck Sharp & Dohme Corp. | 3'-pyridyl substituted- 6,6-difluoro bicyclic himbacine derivatives |
| WO2015089842A1 (en) * | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Novel tricyclic calcium sensing receptor antagonists for the treatment of osteoporosis |
| CN108912142B (zh) * | 2018-08-08 | 2021-06-18 | 延边大学 | 吡咯并苯并恶嗪酮类化合物及其注射剂和在抗血栓中的用途 |
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| CA2048003A1 (en) * | 1990-08-21 | 1992-02-22 | Serge Burner | Tricyclic pyridone derivatives |
| USRE38452E1 (en) * | 1993-07-27 | 2004-03-02 | Pharmacia & Upjohn Company | Heterocyclic amines having central nervous system activity |
| US6063847A (en) * | 1997-11-25 | 2000-05-16 | Schering Corporation | Thrombin receptor antagonists |
| IT1313682B1 (it) * | 1999-11-25 | 2002-09-09 | Archimica Spa | Procedimento per la preparazione di (s)-n-terbutil-1,2,3,4-tetraidroisochinolin-3-carbossiammide. |
| DE60131160T2 (de) * | 2000-06-07 | 2008-08-07 | Vertex Pharmaceuticals Inc., Cambridge | Caspase-inhibitoren und ihre verwendungen |
| CZ20024098A3 (cs) | 2000-06-15 | 2003-05-14 | Schering Corporation | Látky, antagonizující receptor thrombinu |
| US7488742B2 (en) * | 2000-06-15 | 2009-02-10 | Schering Corporation | Thrombin receptor antagonists |
| MY139335A (en) * | 2001-10-18 | 2009-09-30 | Schering Corp | Substituted tricyclic himbacine derivatives that are useful as thrombin receptor antagonists |
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| AU2006331703A1 (en) | 2007-07-05 |
| WO2007075809A3 (en) | 2008-02-21 |
| CN101384590A (zh) | 2009-03-11 |
| US7888369B2 (en) | 2011-02-15 |
| EP1966203B1 (en) | 2013-11-13 |
| WO2007075809A2 (en) | 2007-07-05 |
| US20070149518A1 (en) | 2007-06-28 |
| JP2009521458A (ja) | 2009-06-04 |
| ZA200806065B (en) | 2009-07-29 |
| TW200732330A (en) | 2007-09-01 |
| IL192308A0 (en) | 2009-02-11 |
| KR20080083672A (ko) | 2008-09-18 |
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