CN102282128B - 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂 - Google Patents
用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂 Download PDFInfo
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D277/54—Nitrogen and either oxygen or sulfur atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
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- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/51—Y being a hydrogen or a carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
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- C—CHEMISTRY; METALLURGY
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Abstract
Description
蛋白 | 探针 | 蛋白(nM) | 探针(nM) | 抗体 | 抗体(nM) |
GST-Bcl-2 | F-Bak肽探针乙酰基-(SEQ ID NO: 1 GQVGRQLAIIGDK(6-FAM)SEQ ID NO: 2 INR-酰胺) | 1 | 100 | Tb-抗-GST | 1 |
实施例编号 | TR-FRET结合:Bcl-2 Ki(μM) | 实施例编号 | TR-FRET结合:Bcl-2 Ki(μM) |
1 | 0.051449 | 25 | 0.372106 |
2 | 0.082918 | 26 | 0.393356 |
3 | 0.051702 | 27 | 0.433996 |
5 | 0.176183 | 28 | 0.417285 |
6 | 0.703735 | 29 | 0.339986 |
7 | 0.000084 | 30 | 0.269175 |
8 | 0.000064 | 31 | 0.138755 |
9 | 0.000307 | 32 | 0.43792 |
10 | 0.743178 | 33 | 0.000649 |
11 | 0.177064 | 34 | 0.001791 |
12 | 0.392534 | 35 | 0.002067 |
13 | 0.387693 | 36 | 0.293805 |
14 | 0.408575 | 39 | 0.020238 |
15 | 0.282112 | 40 | 0.000407 |
16 | 0.037859 | 41 | 0.000053 |
17 | 0.356257 | 42 | 0.000039 |
18 | 0.128531 | 43 | 0.046497 |
19 | 0.234118 | 44 | 0.024776 |
20 | 0.048076 | 45 | 0.0067348 |
22 | 0.188226 | 46 | 0.0017502 |
23 | 0.447133 | 47 | 0.020416 |
24 | 0.3421 | 48 | 0.001637 |
Claims (8)
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Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI3330293T1 (sl) * | 2008-11-07 | 2019-10-30 | Amgen Res Munich Gmbh | Zdravljenje pediatrične akutne limfoblastne levkemije z bispecifičnimi protitelesi proti CD3XCD19 |
DK2342227T3 (en) | 2008-11-07 | 2016-02-15 | Amgen Res Munich Gmbh | TREATMENT OF ACUTE Lymphoblastic Tissue Leukemia |
US8557983B2 (en) | 2008-12-04 | 2013-10-15 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US20100160322A1 (en) | 2008-12-04 | 2010-06-24 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US8563735B2 (en) | 2008-12-05 | 2013-10-22 | Abbvie Inc. | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
US8586754B2 (en) * | 2008-12-05 | 2013-11-19 | Abbvie Inc. | BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
CA2747835A1 (en) * | 2009-01-19 | 2010-07-22 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
CN102282128B (zh) | 2009-01-19 | 2015-06-17 | Abbvie公司 | 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂 |
US20220315555A1 (en) | 2009-05-26 | 2022-10-06 | Abbvie Inc. | Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases |
US8546399B2 (en) | 2009-05-26 | 2013-10-01 | Abbvie Inc. | Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases |
US9034875B2 (en) | 2009-05-26 | 2015-05-19 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
KR101920202B1 (ko) * | 2009-05-26 | 2018-11-21 | 애브비 아일랜드 언리미티드 컴퍼니 | 암,면역 질환 및 자가면역 질환의 치료를 위한 아폽토시스-유도제 |
PT2550258E (pt) | 2010-03-25 | 2015-11-30 | Abbvie Inc | Agentes indutores de apoptose para o tratamento de cancro e de doenças imunitárias e autoimunes |
RU2598345C2 (ru) | 2010-10-29 | 2016-09-20 | Эббви Инк. | Твердые дисперсии, содержащие средства, вызывающие апоптоз |
UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
PT2642999T (pt) | 2010-11-23 | 2017-01-05 | Abbvie Ireland Unlimited Co | Métodos de tratamento que utilizam inibidores seletivos de bcl-2 |
BR112013012740A2 (pt) | 2010-11-23 | 2016-09-13 | Abbvie Inc | sais e formas cristalinas de um agente que induz apoptose |
CN102584744B (zh) * | 2011-01-06 | 2015-07-01 | 上海药明康德新药开发有限公司 | 4-(4-((2-(4-氯苯基)-5,5-二甲基环己基-1-烯)甲基)哌嗪-1-基)苯甲酸的合成方法 |
SG11201400150TA (en) | 2011-09-30 | 2014-03-28 | Regeneron Pharma | Anti-erbb3 antibodies and uses thereof |
US20140275082A1 (en) | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
HRP20211813T1 (hr) | 2014-08-11 | 2022-03-04 | Acerta Pharma B.V. | Terapeutske kombinacije inhibitora btk i inhibitora bcl-2 |
US10195213B2 (en) | 2015-03-13 | 2019-02-05 | Unity Biotechnology, Inc. | Chemical entities that kill senescent cells for use in treating age-related disease |
KR20190026771A (ko) * | 2016-06-20 | 2019-03-13 | 럿거스, 더 스테이트 유니버시티 오브 뉴 저지 | 치료 화합물 |
BR112019001666A2 (pt) | 2016-08-05 | 2019-05-28 | Univ Michigan Regents | n-(fenilsulfonil)benzamidas e compostos relacionados como inibidores de bcl-2 |
WO2018127130A1 (en) | 2017-01-07 | 2018-07-12 | Shanghai Fochon Pharmaceutical Co., Ltd. | Compounds as bcl-2-selective apoptosis-inducing agents |
CA3057886A1 (en) | 2017-04-18 | 2018-10-25 | Shanghai Fochon Pharmaceutical Co., Ltd. | Bcl-2 inhibitors as apoptosis-inducing agents |
CN111801320A (zh) | 2018-01-10 | 2020-10-20 | 里科瑞尔姆Ip控股有限责任公司 | 苯甲酰胺化合物 |
WO2019193161A1 (en) | 2018-04-06 | 2019-10-10 | Universität Wien | Bumetanide derivatives for the therapy of stroke and other neurological diseases/disorders involving nkccs |
AU2019247641A1 (en) | 2018-04-06 | 2020-11-12 | Zilentin AG | Bumetanide derivatives for the therapy of hyperhidrosis |
BR112020022092A2 (pt) | 2018-04-29 | 2021-02-02 | Beigene, Ltd. | compostos, método para tratar doenças apoptóticas desreguladas e composição farmacêutica |
AU2020326154A1 (en) * | 2019-08-06 | 2022-02-24 | Basf Coatings Gmbh | Method and system for matching and adjusting pigmentation of a sample coating to a target coating |
US20210056575A1 (en) * | 2019-08-21 | 2021-02-25 | EquipX, LLC | System and method for evaluating medical equipment |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1688580A (zh) * | 2002-08-08 | 2005-10-26 | 记忆药物公司 | 作为磷酸二酯酶4抑制剂的2-三氟甲基-6-氨基嘌呤衍生物 |
CN1863798A (zh) * | 2003-10-03 | 2006-11-15 | 博尔托拉制药公司 | 2,4-二氧代-3-喹唑啉基芳基磺酰基脲 |
CN101175738A (zh) * | 2005-05-12 | 2008-05-07 | 艾博特公司 | 细胞凋亡促进剂 |
Family Cites Families (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GR80917B (en) | 1983-11-14 | 1985-03-13 | Dow Chemical Co | Novel substituted 1,2,4-triazolo (1,5-a) pyrimidine-2-sulfonamides and compositions and methods of controlling undesired vegetation and suppressing the nitrification of ammonium nitrogen in soil |
DE3781769T2 (de) * | 1986-10-31 | 1993-02-11 | Duphar Int Res | 1-carbamoyl-2-pyrazolin-derivate mit herbizidischer wirkung. |
MY115155A (en) | 1993-09-09 | 2003-04-30 | Upjohn Co | Substituted oxazine and thiazine oxazolidinone antimicrobials. |
JPH11512429A (ja) | 1995-09-15 | 1999-10-26 | ファルマシア・アンド・アップジョン・カンパニー | アミノアリールオキサゾリジノン n−オキシド |
US20030220234A1 (en) | 1998-11-02 | 2003-11-27 | Selvaraj Naicker | Deuterated cyclosporine analogs and their use as immunodulating agents |
US6492389B1 (en) * | 1998-07-21 | 2002-12-10 | Thomas Jefferson University | Small molecule inhibitors of BCL-2 proteins |
GB9918037D0 (en) | 1999-07-30 | 1999-09-29 | Biochemie Gmbh | Organic compounds |
WO2001019814A2 (en) | 1999-09-14 | 2001-03-22 | Merck Frosst Canada & Co. | Carboxylic acids and acylsulfonamides, compositions containing such compounds and methods of treatment |
NZ523987A (en) | 2000-08-09 | 2004-10-29 | Astrazeneca Ab | Indole, azaindole and indazole derivatives having VEGF inhibiting activity |
US6331651B1 (en) | 2000-09-18 | 2001-12-18 | E. I. Du Pont De Nemours And Company | Process for making hexamethylene diamine using ozone-treated adiponitrile that contains phosphorous compounds |
US6720338B2 (en) * | 2000-09-20 | 2004-04-13 | Abbott Laboratories | N-acylsulfonamide apoptosis promoters |
AR031130A1 (es) | 2000-09-20 | 2003-09-10 | Abbott Lab | N-acilsulfonamidas promotoras de la apoptosis |
GB0212785D0 (en) * | 2002-05-31 | 2002-07-10 | Glaxo Group Ltd | Compounds |
JP4336678B2 (ja) | 2003-09-04 | 2009-09-30 | 株式会社日立超エル・エス・アイ・システムズ | 半導体装置 |
WO2005049593A2 (en) | 2003-11-13 | 2005-06-02 | Abbott Laboratories | N-acylsulfonamide apoptosis promoters |
US7767684B2 (en) * | 2003-11-13 | 2010-08-03 | Abbott Laboratories | Apoptosis promoters |
US7642260B2 (en) * | 2003-11-13 | 2010-01-05 | Abbott Laboratories, Inc. | Apoptosis promoters |
US7973161B2 (en) * | 2003-11-13 | 2011-07-05 | Abbott Laboratories | Apoptosis promoters |
WO2005099353A2 (en) | 2004-04-19 | 2005-10-27 | Symed Labs Limited | A novel process for the preparation of linezolid and related compounds |
DE602004020812D1 (de) | 2004-07-20 | 2009-06-04 | Symed Labs Ltd | Neue zwischenprodukte für linezolid und verwandte verbindungen |
JP2008514702A (ja) | 2004-09-29 | 2008-05-08 | エーエムアール テクノロジー インコーポレイテッド | 新規シクロスポリン類似体およびそれらの薬学的使用 |
TW200716636A (en) | 2005-05-31 | 2007-05-01 | Speedel Experimenta Ag | Heterocyclic spiro-compounds |
US7514068B2 (en) | 2005-09-14 | 2009-04-07 | Concert Pharmaceuticals Inc. | Biphenyl-pyrazolecarboxamide compounds |
TWI389895B (zh) | 2006-08-21 | 2013-03-21 | Infinity Discovery Inc | 抑制bcl蛋白質與結合夥伴間之交互作用的化合物及方法 |
US7842681B2 (en) * | 2006-09-05 | 2010-11-30 | Abbott Laboratories | Treatment of myeoproliferative diseases |
EP2061772A4 (en) | 2006-09-11 | 2011-06-29 | Curis Inc | MULTIFUNCTIONAL SMALL MOLECULES AS PROLIFERATION-ACTIVE ACTIVE SUBSTANCES |
US8796267B2 (en) | 2006-10-23 | 2014-08-05 | Concert Pharmaceuticals, Inc. | Oxazolidinone derivatives and methods of use |
WO2008064116A2 (en) * | 2006-11-16 | 2008-05-29 | Abbott Laboratories | Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection |
KR101222412B1 (ko) | 2007-02-15 | 2013-01-15 | 에프. 호프만-라 로슈 아게 | Taar1 리간드로서의 2-아미노옥사졸린 |
KR20100105802A (ko) | 2007-04-19 | 2010-09-29 | 콘서트 파마슈티컬즈, 인크. | 중수소화된 모르폴리닐 화합물 |
US7531685B2 (en) | 2007-06-01 | 2009-05-12 | Protia, Llc | Deuterium-enriched oxybutynin |
WO2009035598A1 (en) | 2007-09-10 | 2009-03-19 | Concert Pharmaceuticals, Inc. | Deuterated pirfenidone |
WO2009036035A1 (en) | 2007-09-10 | 2009-03-19 | Curis, Inc. | Bcl-2 inhibitors |
WO2009036051A1 (en) | 2007-09-10 | 2009-03-19 | Curis, Inc. | Bcl-2 inhibitors containing a zinc binding moiety |
US20090118238A1 (en) | 2007-09-17 | 2009-05-07 | Protia, Llc | Deuterium-enriched alendronate |
US20090088416A1 (en) | 2007-09-26 | 2009-04-02 | Protia, Llc | Deuterium-enriched lapaquistat |
US20090082471A1 (en) | 2007-09-26 | 2009-03-26 | Protia, Llc | Deuterium-enriched fingolimod |
US20090137457A1 (en) | 2007-10-02 | 2009-05-28 | Concert Pharmaceuticals, Inc. | Pyrimidinedione derivatives |
US8410124B2 (en) | 2007-10-18 | 2013-04-02 | Concert Pharmaceuticals Inc. | Deuterated etravirine |
US20090105338A1 (en) | 2007-10-18 | 2009-04-23 | Protia, Llc | Deuterium-enriched gabexate mesylate |
AU2008317375B2 (en) | 2007-10-26 | 2013-02-28 | Concert Pharmaceuticals, Inc. | Deuterated darunavir |
US20100160322A1 (en) * | 2008-12-04 | 2010-06-24 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US8557983B2 (en) * | 2008-12-04 | 2013-10-15 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US8563735B2 (en) * | 2008-12-05 | 2013-10-22 | Abbvie Inc. | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
CA2747835A1 (en) * | 2009-01-19 | 2010-07-22 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
CN102282128B (zh) | 2009-01-19 | 2015-06-17 | Abbvie公司 | 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂 |
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- 2010-01-15 KR KR1020117018663A patent/KR20110116161A/ko not_active Application Discontinuation
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- 2012-11-20 US US13/682,603 patent/US9156856B2/en not_active Expired - Fee Related
-
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- 2015-09-15 US US14/855,176 patent/US9493431B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1688580A (zh) * | 2002-08-08 | 2005-10-26 | 记忆药物公司 | 作为磷酸二酯酶4抑制剂的2-三氟甲基-6-氨基嘌呤衍生物 |
CN1863798A (zh) * | 2003-10-03 | 2006-11-15 | 博尔托拉制药公司 | 2,4-二氧代-3-喹唑啉基芳基磺酰基脲 |
CN101175738A (zh) * | 2005-05-12 | 2008-05-07 | 艾博特公司 | 细胞凋亡促进剂 |
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CA2747837A1 (en) | 2010-07-22 |
EP2387559B1 (en) | 2016-06-29 |
JP5613177B2 (ja) | 2014-10-22 |
EP2387559A1 (en) | 2011-11-23 |
AU2010204555A1 (en) | 2011-08-04 |
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US20130184278A1 (en) | 2013-07-18 |
EP3095784A1 (en) | 2016-11-23 |
CN104945311A (zh) | 2015-09-30 |
ZA201104671B (en) | 2012-03-28 |
MX2011007684A (es) | 2011-08-08 |
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