AR061083A1 - Derivados de cicloalquilaminoacidos y composiciones farmaceuticas que los contienen - Google Patents
Derivados de cicloalquilaminoacidos y composiciones farmaceuticas que los contienenInfo
- Publication number
- AR061083A1 AR061083A1 ARP070102020A ARP070102020A AR061083A1 AR 061083 A1 AR061083 A1 AR 061083A1 AR P070102020 A ARP070102020 A AR P070102020A AR P070102020 A ARP070102020 A AR P070102020A AR 061083 A1 AR061083 A1 AR 061083A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- heteroaryl
- cycloalkyl
- heterocyclyl
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 239000002253 acid Substances 0.000 title 1
- 150000007513 acids Chemical class 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 22
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 20
- 125000000623 heterocyclic group Chemical group 0.000 abstract 19
- 125000003118 aryl group Chemical group 0.000 abstract 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 16
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 15
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 150000002367 halogens Chemical class 0.000 abstract 13
- 229910052739 hydrogen Inorganic materials 0.000 abstract 13
- 239000001257 hydrogen Substances 0.000 abstract 13
- 125000000304 alkynyl group Chemical group 0.000 abstract 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 125000003545 alkoxy group Chemical group 0.000 abstract 8
- 150000002431 hydrogen Chemical class 0.000 abstract 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 102200160920 rs35304565 Human genes 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000002619 bicyclic group Chemical group 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
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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
- A61K31/4245—Oxadiazoles
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Abstract
Se refiere a compuestos de Formula 1 y a sales farmacéuticamente aceptables, profármacos, solvatos o hidratos de los mismos. También se refiere a un método de uso de tales compuestos en el tratamiento de enfermedades hiperproliferativas y enfermedades autoinmunes de mamíferos, especialmente en seres humanos, y a composiciones farmacéuticas que contienen tales compuestos. Reivindicacion 1: Un compuesto de formula (1) o una sal farmacéuticamente aceptable del mismo, en la que B se selecciona entre el grupo que consiste en fenilo y un anillo heteroarilo (de 5 a 6 miembros); D se selecciona entre el grupo que consiste en fenilo y un anillo heteroarilo (de 5 a 6 miembros); E se selecciona entre el grupo que consiste en fenilo y un anillo heteroarilo (de 5 a 6 miembros); R1 es un radical seleccionado entre el grupo que consiste en hidrogeno, alquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)-, heteroaril (C1-12)-, R7- SO2-, , R7-C(O)-, R7O-C(O)- y (R7)2N-C(O)-; donde cada uno de dichos radicales alquil (C1-6)-, alquenil C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)-, heteroaril (C1-12)-, R7-SO2-, R7-C(O)-, R7O-C(O)- y (R7)2N- C(O)-R1 puede estar opcionalmente sustituido con uno a tres restos seleccionados independientemente entre el grupo que consiste en hidrogeno, hidroxi, halogeno, -CN, alquil (C1-6)-, alcoxi (C1-6)-, perhaloalquil (C1-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)- y heteroaril (C1-12)-; cada R2 es un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, hidroxi, halogeno, -CN, alquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3- 7)-, heterociclil (C2-9)-, aril (C6-10)- y heteroaril (C1-12)-; donde cada uno de dichos radicales alquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)- y heteroaril (C1-12)- R2 puede estar opcionalmente sustituido con uno a tres restos seleccionados independientemente entre el grupo que consiste en hidrogeno, hidroxi, halogeno, -CN, alquil (C1-6)-, perhaloalquil (C1-4)-, perhaloalcoxi (C1-4)-, cicloalquil (C3-7)-, heterociclil (C2-9)- , aril (C6-10)- y heteroaril (C1-12)-; cada r3 es un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, halogeno, hidroxi, -CN, alquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, alcoxi (C1-6)-, perhaloalquil (C1-6)- y perhaloalcoxi (C1-6)-; cada R4 es un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, halogeno, hidroxi, -CN, -N(R6)2, alquil (C1-6)-, alquenil (C2-6)-, alquinil (C3-6)-, alcoxi (C1-6)-, perhaloalquil (C1-6)-, alquil (C1-6)-S(O)k-, R10C(O)N(R10)-, (R10)2NC(O)-, R10C(O)-, R10OC(O)-, (R10)2NC(O)N(R10)-, (R10)2NS(O)-, (R10)2NS(O)2-, cicloalquil (C3-7)-, aril (C6-10)-, heterociclil (C2-9)- y heteroaril (C1-12)-; donde cada uno de dichos radicales alquil (C1-6)-, alquenil (C2-6)-, alquinil (C3-6)-, alcoxi (C1-6)-, alquil (C1-6)-S(O)k-, R10C(O)N(R10)-, (R10)2NC(O)-, R10C(O)-, R10OC(O)-, (R10)2NC(O)N(R10)-, (R10)2NS(O)-, (R10)2NS(O)2-, cicloalquil(C3-7)-, aril (C6-10)-, heterociclil (C2-9)- y heteroaril (C1-12)-R4 puede estar opcionalmente sustituido con uno a cinco restos seleccionados independientemente entre el grupo que consiste en halogeno, hidroxi, -CN, alquil (C1-6)-, cicloalquil (C3-7)-, alcoxi (C1-6)- y perhaloalcoxi (C1-6)-; R5 es un radical seleccionado entre el grupo que consiste en hidrogeno, halogeno, -CN, alquil (C1-10)-, alcoxi (C1-6)-, alquenil (C2-10)-, alquinil (C2-10)-, cicloalquil (C3-7)-, aril (C6-10)-, heterociclil (C2-9)-, heteroaril (C1-12)-, cicloalquil (C3-7)-O-, aril (C6-10)-O-, heterociclil (C2-9)-O-, heteroaril (C1-12)-O-, R7-S-, R7-SO-, R7-SO2-, R7-C(O)-, R7-C(O)-O-, R7O-C(O)- y (R7)2N-C(O)-; donde cada uno de dichos radicales alquil (C1-10)-, alcoxi (C1-6)- y alquinil (C2-10)-R5 puede estar opcionalmente sustituido con uno a cinco restos seleccionados independientemente entre el grupo que consiste en halogeno, hidroxi, -CN, alquil (C1-6), cicloalquil (C3-7)-, aril (C6-10)-, alcoxi (C1-6)-, heterociclil (C2-9)- y heteroaril (C1-12)-; donde cada uno de dichos radicales cicloalquil (C3-7)- y cicloalquil (C3-7)-O-R5 puede estar opcionalmente sustituido con uno a cinco restos seleccionados independientemente entre el grupo que consiste en halogeno, hidroxi, -CN, alquil (C1- 6)-, aril (C6-10)-, alcoxi (C1-6)-, heterociclil (C2-9)- y heteroaril (C1-12)-; donde cada uno de dichos radicales aril (C6-10)-, heterociclil (C2-9)-, heteroaril (C1-12)-, aril (C6-10)-O-, heterociclil (C2-9)-O- y heteroaril (C1-12)-O-R5 puede estar opcionalmente sustituido con uno a cinco restos seleccionados independientemente entre el grupo que consiste en halogeno, hidroxi, -CN, alquil (C1-6)- y alcoxi (C1-6)-; donde cada uno de dichos radicales R7-S-, R7-SO-, R7-SO2-, R7-C(O)-, R7- C(O)-O-, R7O-C(O)- y (R7)2N-C(O)-R5 puede estar opcionalmente sustituido con uno a cinco restos seleccionados independientemente entre el grupo que consiste en halogeno, hidroxi, -CN, alquil (C1-6)-, cicloalquil (C3-7)- y alcoxi (C1-6)-; donde cada uno de los restos alquil (C1-6)-, alcoxi (C1-6)-, aril (C6-10)-, alcoxi (C1-6)-, heterociclil (C2-9)- y heteroaril (C1-12)- mencionados anteriormente para cada uno de los radicales R5 mencionados anteriormente puede estar opcionalmente sustituido con uno a cinco grupos halogeno; opcionalmente dicho radical R5 y un radical R4 o dos radicales R4 pueden tomarse junto con E para formar un anillo bicíclico condensado (de 8 a 10 miembros) que contiene opcionalmente de 1 a 4 heteroátomos seleccionados entre el grupo que consiste en O, S o N(R6); donde dicho anillo bicíclico condensado (de 8 a 10 miembros) está opcionalmente sustituido adicionalmente con uno a dos grupos oxo (=O); cada R6 en un enlace o un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, alquil (C1-6)-, -CN y perhaloalquil (C1-6)-; cada R7 es un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, -CN, alquil (C1-6)-, perhaloalquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)- y heteroaril (C1-12)-; cada R8 es un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, hidroxi, halogeno, -CN, -NH(R)), alquil (C1-6)-, perhaloalquil (C1-6)- y alcoxi (C1-6)-; donde cada uno de dichos radicales alquil (c1-6)- y alcoxi (c1-6)-R8 está opcionalmente sustituido con uno a cinco restos seleccionados entre el grupo que consiste en perhaloalquil (C1-6)-, - O(R9) y -N(R9)2; cada R9 es un radical seleccionado independientemente entre el grupo que consiste en hidrogeno, alquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)-, heteroaril (C1-12)-, R7-S- , R7-SO-, R7-SO2-, R7-C(O)-, R7-C(O)-O-, R7O-C(O)- y (R7)2N-C(O)-; donde cada uno de dichos radicales alquil (C1-6)-, alquenil (C2-6)-, alquinil (C2-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)-, heteroaril (C1-12)-R9 está opcionalmente sustituido con uno a tres restos seleccionados independientementes entre el grupo que consiste en hidrogeno, hidroxi, halogeno, -CN, alquil (C1-6)-, alcoxi (C1-6)-, perhaloalquil (C1-6)-, cicloalquil (C3-7)-, heterociclil (C2-9)-, aril (C6-10)- y heteroaril (C1-12)-; cada R10 es un radical seleccionado entre el grupo que consiste en hidrogeno y alquil (C1-6)-; k es un numero entero de 0 a 2; cada uno de m y n es independientemente un numero entero de 0 a 3; p es un numero entero de 1 a 2; q es un numero entero de 0 a 2; y cada uno de r, s, t y u es independientemente un numero entero de 0 a 4.
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Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2008013990A (es) * | 2006-05-09 | 2009-01-29 | Pfizer Prod Inc | Derivados de cicloalquilamino acidos. |
| CN101511827B (zh) | 2006-09-07 | 2012-02-01 | 埃科特莱茵药品有限公司 | 作为免疫调制剂的吡啶-4-基衍生物 |
| CA2661315C (en) | 2006-09-08 | 2015-11-24 | Actelion Pharmaceuticals Ltd | Pyridin-3-yl derivatives as immunomodulating agents |
| CN101522645B (zh) | 2006-09-21 | 2013-01-09 | 埃科特莱茵药品有限公司 | 苯衍生物及其免疫调节剂的用途 |
| MX2009006304A (es) | 2006-12-15 | 2009-06-23 | Abbott Lab | Nuevos compuestos de oxadiazol. |
| US20110207704A1 (en) * | 2006-12-15 | 2011-08-25 | Abbott Laboratories | Novel Oxadiazole Compounds |
| SI2125797T1 (sl) | 2007-03-16 | 2014-03-31 | Actelion Pharmaceuticals Ltd. | Derivati amino-piridina kot agonisti receptorja s1p1/edg1 |
| GB0706633D0 (en) * | 2007-04-04 | 2007-05-16 | Cyclacel Ltd | Combination |
| CA2703987A1 (en) * | 2007-11-08 | 2009-05-14 | Pfizer Inc. | Cyclobutyl carboxylic acid derivatives |
| CA2710345C (en) * | 2007-12-21 | 2016-11-15 | Merck Serono S.A. | Triazole oxadiazoles derivatives |
| EP2262799B1 (en) * | 2008-03-06 | 2012-07-04 | Actelion Pharmaceuticals Ltd. | Pyridine compounds |
| US20110046170A1 (en) * | 2008-03-06 | 2011-02-24 | Martin Bolli | Novel pyrimidine-pyridine derivatives |
| AU2009220893A1 (en) | 2008-03-07 | 2009-09-11 | Actelion Pharmaceuticals Ltd | Novel aminomethyl benzene derivatives |
| NZ588438A (en) * | 2008-03-07 | 2012-05-25 | Actelion Pharmaceuticals Ltd | Pyridin-2-yl oxadiazole derivatives as immunomodulating agents |
| WO2009131090A1 (ja) * | 2008-04-21 | 2009-10-29 | 旭化成ファーマ株式会社 | アミノ酸化合物 |
| KR20190004843A (ko) | 2008-07-23 | 2019-01-14 | 아레나 파마슈티칼스, 인크. | 자가면역성 및 염증성의 장애의 치료에 유용한 치환된 1,2,3,4-테트라히드로시클로펜타[b]인돌-3-일)아세트산 유도체 |
| AU2009288738B9 (en) | 2008-08-27 | 2015-04-16 | Arena Pharmaceuticals, Inc. | Substituted tricyclic acid derivatives as S1P1 receptor agonists useful in the treatment of autoimmune and inflammatory disorders |
| CA2752804C (en) * | 2009-03-03 | 2017-04-04 | Anna Quattropani | Oxazole pyridine derivatives useful as s1p1 receptor agonists |
| EP2454255B1 (en) | 2009-07-16 | 2013-11-06 | Actelion Pharmaceuticals Ltd. | Pyridin-4-yl derivatives as s1p1/edg1 agonists |
| TW201120016A (en) * | 2009-12-08 | 2011-06-16 | Abbott Lab | Novel oxadiazole compounds |
| SG10201500639TA (en) | 2010-01-27 | 2015-03-30 | Arena Pharm Inc | Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof |
| SG183416A1 (en) | 2010-03-03 | 2012-09-27 | Arena Pharm Inc | Processes for the preparation of s1p1 receptor modulators and crystalline forms thereof |
| JP5869579B2 (ja) * | 2010-09-24 | 2016-02-24 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 置換オキサジアゾール化合物およびそれらのs1p1アゴニストとしての使用 |
| ES2544086T3 (es) | 2011-01-19 | 2015-08-27 | Actelion Pharmaceuticals Ltd. | Derivados de 2-metoxi-piridin-4-ilo |
| EP2511275A1 (en) | 2011-04-12 | 2012-10-17 | Bioprojet | Novel piperidinyl monocarboxylic acids as S1P1 receptor agonists |
| DE102011083271A1 (de) | 2011-09-23 | 2013-03-28 | Beiersdorf Ag | Aromatische Amidothiazole, deren kosmetische oder dermatologische Verwendung sowie kosmetische oder dermatologische Zubereitungen mit einem Gehalt an solchen Aromatischen Amidothiazolen |
| US9950194B2 (en) | 2014-09-09 | 2018-04-24 | Mevion Medical Systems, Inc. | Patient positioning system |
| PL3242666T3 (pl) | 2015-01-06 | 2025-02-17 | Arena Pharmaceuticals, Inc. | Związek do zastosowania w leczeniu dolegliwości związanych z receptorem s1p1 |
| PH12017502097B1 (en) | 2015-05-20 | 2023-05-05 | Idorsia Pharmaceuticals Ltd | Crystalline form of the compound (s)-3-{4-[5-(2-cyclopentyl-6-methoxy-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenoxy}-propane-1,2-diol |
| JP6838744B2 (ja) | 2015-06-22 | 2021-03-03 | アリーナ ファーマシューティカルズ, インコーポレイテッド | S1P1レセプター関連障害における使用のための(R)−2−(7−(4−シクロペンチル−3−(トリフルオロメチル)ベンジルオキシ)−1,2,3,4−テトラヒドロシクロペンタ[b]インドール−3−イル)酢酸(化合物1)の結晶性L−アルギニン塩 |
| AU2018220521A1 (en) | 2017-02-16 | 2019-09-05 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| CA3053416A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of inflammatory bowel disease with extra-intestinal manifestations |
| CN109956912B (zh) * | 2017-12-26 | 2021-10-22 | 中国医学科学院药物研究所 | 含二苯基噁二唑的羧酸类化合物、其制备方法及医药用途 |
| CR20200347A (es) | 2018-02-13 | 2020-09-23 | Gilead Sciences Inc | Inhibidores pd-1/pd-l1 |
| KR102591947B1 (ko) | 2018-04-19 | 2023-10-25 | 길리애드 사이언시즈, 인코포레이티드 | Pd-1/pd-l1 억제제 |
| KR102859841B1 (ko) | 2018-06-06 | 2025-09-12 | 아레나 파마슈티칼스, 인크. | S1p1 수용체와 관련된 병태의 치료 방법 |
| PT3820572T (pt) | 2018-07-13 | 2023-11-10 | Gilead Sciences Inc | Inibidores pd-1/pd-l1 |
| CN119751336A (zh) | 2018-09-06 | 2025-04-04 | 艾尼纳制药公司 | 可用于治疗自身免疫性病症和炎性病症的化合物 |
| JP7158577B2 (ja) | 2018-10-24 | 2022-10-21 | ギリアード サイエンシーズ, インコーポレイテッド | Pd-1/pd-l1阻害剤 |
| USD937488S1 (en) | 2020-10-05 | 2021-11-30 | Jonathan R. Barnes | Pair of nail clipper handles |
Family Cites Families (79)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8607683D0 (en) | 1986-03-27 | 1986-04-30 | Ici Plc | Anti-tumor agents |
| PH30484A (en) | 1990-02-19 | 1997-05-28 | Ciba Geigy | Acy compounds pharmaceutical composition containing said compound and method of use thereof |
| SG64322A1 (en) | 1991-05-10 | 1999-04-27 | Rhone Poulenc Rorer Int | Bis mono and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase |
| NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
| FI941572L (fi) | 1991-10-07 | 1994-05-27 | Oncologix Inc | Anti-erbB-2-monoklonaalisten vasta-aineiden yhdistelmä ja käyttömenetelmä |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| ATE503496T1 (de) | 1992-02-06 | 2011-04-15 | Novartis Vaccines & Diagnostic | Biosynthetisches bindeprotein für tumormarker |
| US6177401B1 (en) | 1992-11-13 | 2001-01-23 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften | Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis |
| GB9323290D0 (en) | 1992-12-10 | 1994-01-05 | Zeneca Ltd | Quinazoline derivatives |
| GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
| GB9314884D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Tricyclic derivatives |
| US5466823A (en) | 1993-11-30 | 1995-11-14 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| US5608082A (en) | 1994-07-28 | 1997-03-04 | Agouron Pharmaceuticals, Inc. | Compounds useful as antiproliferative agents and GARFT inhibitors |
| GB9510757D0 (en) | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
| US5814464A (en) | 1994-10-07 | 1998-09-29 | Regeneron Pharma | Nucleic acids encoding TIE-2 ligand-2 |
| GB9424233D0 (en) | 1994-11-30 | 1995-01-18 | Zeneca Ltd | Quinazoline derivatives |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| GB9518953D0 (en) | 1995-09-15 | 1995-11-15 | Pfizer Ltd | Pharmaceutical formulations |
| GB9520822D0 (en) | 1995-10-11 | 1995-12-13 | Wellcome Found | Therapeutically active compounds |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
| JPH11512750A (ja) | 1996-06-27 | 1999-11-02 | ファイザー インク. | 2―(2―オキソ―エチリデン)―イミダゾリジン―4―オンの誘導体およびファルネシル蛋白質トランスフェラーゼ阻害物質としてのそれらの使用法 |
| EP0912559B1 (en) | 1996-07-13 | 2002-11-06 | Glaxo Group Limited | Fused heterocyclic compounds as protein tyrosine kinase inhibitors |
| HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
| ES2191187T3 (es) | 1996-07-13 | 2003-09-01 | Glaxo Group Ltd | Compuestos heteroaromaticos biciclicos como inhibidores de la proteina tirosin-quinasa. |
| WO2000035298A1 (en) | 1996-11-27 | 2000-06-22 | Wm. Wrigley Jr. Company | Chewing gum containing medicament active agents |
| CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| US6316429B1 (en) | 1997-05-07 | 2001-11-13 | Sugen, Inc. | Bicyclic protein kinase inhibitors |
| WO1998054093A1 (en) | 1997-05-30 | 1998-12-03 | Merck & Co., Inc. | Novel angiogenesis inhibitors |
| US6294532B1 (en) | 1997-08-22 | 2001-09-25 | Zeneca Limited | Oxindolylquinazoline derivatives as angiogenesis inhibitors |
| EP1017682A4 (en) | 1997-09-26 | 2000-11-08 | Merck & Co Inc | NEW ANGIOGENESIS INHIBITORS |
| WO1999017770A1 (en) | 1997-10-06 | 1999-04-15 | Basf Aktiengesellschaft | Indeno[1,2-c]pyrazole derivatives for inhibiting tyrosine kinase activity |
| CN1280580A (zh) | 1997-11-11 | 2001-01-17 | 辉瑞产品公司 | 用作抗癌药的噻吩并嘧啶和噻吩并吡啶衍生物 |
| GB9800575D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| RS49779B (sr) | 1998-01-12 | 2008-06-05 | Glaxo Group Limited, | Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze |
| EP1073435B1 (en) | 1998-04-30 | 2004-07-07 | Abbott GmbH & Co. KG | Substituted tricyclic pyrazole derivatives with protein kinase activity |
| HUP0103617A2 (hu) | 1998-05-29 | 2002-02-28 | Sugen, Inc. | Protein kinázt gátló, pirrolilcsoporttal helyettesített 2-indolszármazékok, e vegyületeket tartalmazó gyógyászati készítmények, valamint e vegyületek alkalmazása |
| UA60365C2 (uk) | 1998-06-04 | 2003-10-15 | Пфайзер Продактс Інк. | Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця |
| IL141239A0 (en) | 1998-08-27 | 2002-03-10 | Pfizer Prod Inc | Alkynyl-substituted quinolin-2-one derivatives useful as anticancer agents |
| CZ2001959A3 (cs) | 1998-09-18 | 2001-12-12 | Basf Aktiengesellschaft | 4-Aminopyrrolopyrimidiny jako inhibitory kinasy |
| CA2344249A1 (en) | 1998-09-18 | 2000-03-30 | Basf Aktiengesellschaft | Pyrrolopyrimidines as protein kinase inhibitors |
| CN1335836A (zh) | 1998-11-06 | 2002-02-13 | 巴斯福股份公司 | 三环吡唑衍生物 |
| EP1006113A1 (en) | 1998-12-02 | 2000-06-07 | Pfizer Products Inc. | Derivatives of 2-(2-oxo-ethylidene)-imidazolidin-4-one and their use to inhibit abnormal cell growth |
| US6682736B1 (en) | 1998-12-23 | 2004-01-27 | Abgenix, Inc. | Human monoclonal antibodies to CTLA-4 |
| JP3270834B2 (ja) | 1999-01-27 | 2002-04-02 | ファイザー・プロダクツ・インク | 抗がん剤として有用なヘテロ芳香族二環式誘導体 |
| UA71945C2 (en) | 1999-01-27 | 2005-01-17 | Pfizer Prod Inc | Substituted bicyclic derivatives being used as anticancer agents |
| TR200201296T2 (tr) | 1999-02-11 | 2002-07-22 | Pfizer Products Inc. | Antikanser maddeleri olarak faydalı heteroaril-ikame edilmiş kinolin-2-on türevleri |
| US6586447B1 (en) | 1999-04-01 | 2003-07-01 | Pfizer Inc | 3,3-disubstituted-oxindole derivatives useful as anticancer agents |
| IL146474A0 (en) | 1999-06-03 | 2002-07-25 | Knoll Gmbh | Benzothiazinone and benzoxazinone compounds |
| TWI262914B (en) | 1999-07-02 | 2006-10-01 | Agouron Pharma | Compounds and pharmaceutical compositions for inhibiting protein kinases |
| ES2298165T3 (es) | 1999-11-22 | 2008-05-16 | Smithkline Beecham Plc | Derivados de imidazol. |
| UA75055C2 (uk) | 1999-11-30 | 2006-03-15 | Пфайзер Продактс Інк. | Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі |
| PT1255752E (pt) | 2000-02-15 | 2007-10-17 | Pharmacia & Upjohn Co Llc | Inibidores de proteína quinases: 2-indolinonas substituídas com pirrolo |
| AU4691601A (en) * | 2000-04-21 | 2001-11-12 | Shionogi & Co | Oxadiazole derivatives having anticancer effects |
| JP4044839B2 (ja) | 2000-06-22 | 2008-02-06 | ファイザー・プロダクツ・インク | 異常細胞増殖を治療するための置換2環式誘導体 |
| AU2002232439A1 (en) | 2000-11-29 | 2002-06-11 | Glaxo Group Limited | Benzimidazole derivatives useful as tie-2 and/or vegfr-2 inhibitors |
| SV2007000775A (es) | 2001-01-05 | 2007-03-15 | Pfizer | Anticuerpos contra el receptor del factor de crecimiento similar a insulina |
| AR042586A1 (es) | 2001-02-15 | 2005-06-29 | Sugen Inc | 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa |
| EP1424078A4 (en) | 2001-09-04 | 2009-03-25 | Ono Pharmaceutical Co | RESPIRATORY DISEASE MEDICINES COMPRISING A SPHINGOSINE-1-PHOSPHATE RECEPTOR REGULATING AGENT |
| US7427623B2 (en) | 2001-09-11 | 2008-09-23 | Smithkline Beecham Corporation | 4-Amino-2,3-disubstituted thieno[2,3-d]pyrimidines and pharmacetical compositions thereof |
| AR039067A1 (es) | 2001-11-09 | 2005-02-09 | Pfizer Prod Inc | Anticuerpos para cd40 |
| US20050070506A1 (en) | 2002-01-18 | 2005-03-31 | Doherty George A. | Selective s1p1/edg1 receptor agonists |
| CA2476281A1 (en) | 2002-02-08 | 2003-08-14 | Smithkline Beecham Corporation | Pyrimidine compounds |
| ATE365165T1 (de) | 2002-03-01 | 2007-07-15 | Smithkline Beecham Corp | Diaminopyrimidine und deren verwendung als angiogenesehemmer |
| US20050215531A1 (en) | 2002-05-16 | 2005-09-29 | Thomas Baumruker | Use of edg receptor binding agents in cancer |
| WO2003105771A2 (en) | 2002-06-17 | 2003-12-24 | Merck & Co., Inc. | 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylates and 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl)pyrrolidine-3-carboxylates as edg receptor agonists |
| PA8580301A1 (es) | 2002-08-28 | 2005-05-24 | Pfizer Prod Inc | Nuevos derivados de benzoimidazol utiles como agentes antiproliferativos |
| WO2004035538A1 (en) | 2002-10-15 | 2004-04-29 | Merck & Co., Inc. | Process for making azetidine-3-carboxylic acid |
| SE0203654D0 (sv) * | 2002-12-09 | 2002-12-09 | Astrazeneca Ab | New compounds |
| BRPI0409097A (pt) * | 2003-04-10 | 2006-04-11 | Avanir Pharmaceuticals | derivados de imidazol para tratamento de distúrbios alérgicos e hiperproliferativos |
| US7071333B2 (en) | 2003-07-30 | 2006-07-04 | Bristol-Myers Squibb Company | Triazolopurine-based tricyclic compounds and pharmaceutical compositions comprising same |
| WO2005058848A1 (en) * | 2003-12-17 | 2005-06-30 | Merck & Co., Inc. | (3,4-disubstituted)propanoic carboxylates as s1p (edg) receptor agonists |
| EP2308879A1 (en) * | 2004-04-02 | 2011-04-13 | OSI Pharmaceuticals, Inc. | 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors |
| US7511062B2 (en) * | 2004-05-18 | 2009-03-31 | Schering Corporation | Substituted 2-quinolyl-oxazoles useful as PDE4 inhibitors |
| MX2008013990A (es) * | 2006-05-09 | 2009-01-29 | Pfizer Prod Inc | Derivados de cicloalquilamino acidos. |
| CA2703987A1 (en) * | 2007-11-08 | 2009-05-14 | Pfizer Inc. | Cyclobutyl carboxylic acid derivatives |
| JP6943759B2 (ja) | 2017-12-28 | 2021-10-06 | 株式会社東海理化電機製作所 | シフト装置 |
-
2007
- 2007-04-26 MX MX2008013990A patent/MX2008013990A/es not_active Application Discontinuation
- 2007-04-26 ME MEP-433/08A patent/MEP43308A/xx unknown
- 2007-04-26 EA EA200802058A patent/EA200802058A1/ru unknown
- 2007-04-26 CN CNA2007800260187A patent/CN101490046A/zh active Pending
- 2007-04-26 AU AU2007251282A patent/AU2007251282A1/en not_active Abandoned
- 2007-04-26 JP JP2009508526A patent/JP4383525B2/ja active Active
- 2007-04-26 BR BRPI0711358-7A patent/BRPI0711358A2/pt not_active IP Right Cessation
- 2007-04-26 EP EP10173690A patent/EP2258700A1/en not_active Withdrawn
- 2007-04-26 KR KR1020087029960A patent/KR20090007792A/ko not_active Abandoned
- 2007-04-26 WO PCT/IB2007/001125 patent/WO2007132307A1/en not_active Ceased
- 2007-04-26 UA UAA200812272A patent/UA91129C2/ru unknown
- 2007-04-26 EP EP07734443A patent/EP2021338A1/en not_active Withdrawn
- 2007-04-26 CA CA002651629A patent/CA2651629A1/en not_active Abandoned
- 2007-04-26 RS RSP-2008/0525A patent/RS20080525A/sr unknown
- 2007-05-04 NL NL2000627A patent/NL2000627C2/nl not_active IP Right Cessation
- 2007-05-07 UY UY30326A patent/UY30326A1/es not_active Application Discontinuation
- 2007-05-08 PE PE2007000558A patent/PE20080091A1/es not_active Application Discontinuation
- 2007-05-08 TW TW096116240A patent/TW200808783A/zh unknown
- 2007-05-08 DO DO2007000092A patent/DOP2007000092A/es unknown
- 2007-05-09 US US11/746,314 patent/US7671043B2/en not_active Expired - Fee Related
- 2007-05-09 AR ARP070102020A patent/AR061083A1/es not_active Application Discontinuation
-
2008
- 2008-10-17 NO NO20084382A patent/NO20084382L/no not_active Application Discontinuation
- 2008-10-21 ZA ZA200809002A patent/ZA200809002B/xx unknown
- 2008-10-27 IL IL194954A patent/IL194954A0/en unknown
- 2008-10-30 CR CR10412A patent/CR10412A/es not_active Application Discontinuation
- 2008-11-06 TN TNP2008000446A patent/TNSN08446A1/en unknown
- 2008-11-07 EC EC2008008870A patent/ECSP088870A/es unknown
- 2008-11-07 MA MA31363A patent/MA30403B1/fr unknown
-
2010
- 2010-01-04 US US12/651,885 patent/US20100120794A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| IL194954A0 (en) | 2009-08-03 |
| AU2007251282A1 (en) | 2007-11-22 |
| MA30403B1 (fr) | 2009-05-04 |
| UY30326A1 (es) | 2008-01-02 |
| EP2258700A1 (en) | 2010-12-08 |
| KR20090007792A (ko) | 2009-01-20 |
| TNSN08446A1 (en) | 2010-04-14 |
| ECSP088870A (es) | 2008-12-30 |
| WO2007132307A1 (en) | 2007-11-22 |
| ZA200809002B (en) | 2009-12-30 |
| RS20080525A (sr) | 2009-09-08 |
| MX2008013990A (es) | 2009-01-29 |
| UA91129C2 (ru) | 2010-06-25 |
| NO20084382L (no) | 2008-11-19 |
| NL2000627C2 (nl) | 2009-03-17 |
| TW200808783A (en) | 2008-02-16 |
| NL2000627A1 (nl) | 2007-11-12 |
| JP4383525B2 (ja) | 2009-12-16 |
| EP2021338A1 (en) | 2009-02-11 |
| EA200802058A1 (ru) | 2009-06-30 |
| PE20080091A1 (es) | 2008-02-14 |
| CR10412A (es) | 2008-11-28 |
| US7671043B2 (en) | 2010-03-02 |
| CN101490046A (zh) | 2009-07-22 |
| DOP2007000092A (es) | 2007-12-31 |
| CA2651629A1 (en) | 2007-11-22 |
| MEP43308A (en) | 2011-02-10 |
| US20070270438A1 (en) | 2007-11-22 |
| US20100120794A1 (en) | 2010-05-13 |
| BRPI0711358A2 (pt) | 2011-09-27 |
| JP2009536190A (ja) | 2009-10-08 |
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