CN101951766A - 凋亡抑制蛋白抑制剂 - Google Patents
凋亡抑制蛋白抑制剂 Download PDFInfo
- Publication number
- CN101951766A CN101951766A CN200980106206XA CN200980106206A CN101951766A CN 101951766 A CN101951766 A CN 101951766A CN 200980106206X A CN200980106206X A CN 200980106206XA CN 200980106206 A CN200980106206 A CN 200980106206A CN 101951766 A CN101951766 A CN 101951766A
- Authority
- CN
- China
- Prior art keywords
- mechome
- tert
- compound
- ome
- butyl group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 0 *C(C(N(C(*)C(*)C1)C1N*)=O)NC(C(*)(*)N*)=O Chemical compound *C(C(N(C(*)C(*)C1)C1N*)=O)NC(C(*)(*)N*)=O 0.000 description 16
- PUJDIJCNWFYVJX-UHFFFAOYSA-N NC(OCc1ccccc1)=O Chemical compound NC(OCc1ccccc1)=O PUJDIJCNWFYVJX-UHFFFAOYSA-N 0.000 description 2
- OUJUSTLXYJWCKV-PJWHXOITSA-N CC(C(C(N(CC1)[C@H](Cc(c(c([nH]2)c3)ccc3F)c2Cl)[C@H]1O)=O)N)OC Chemical compound CC(C(C(N(CC1)[C@H](Cc(c(c([nH]2)c3)ccc3F)c2Cl)[C@H]1O)=O)N)OC OUJUSTLXYJWCKV-PJWHXOITSA-N 0.000 description 1
- VHNDAEBVQSXEQD-YRXYFLHQSA-N CC(C(C(N(CC1)[C@H](Cc(c(c([nH]2)c3)ccc3F)c2Cl)[C@H]1OC(C)=O)=O)NC([C@H](C)N(C)C(OC(C)(C)C)=O)=O)OC Chemical compound CC(C(C(N(CC1)[C@H](Cc(c(c([nH]2)c3)ccc3F)c2Cl)[C@H]1OC(C)=O)=O)NC([C@H](C)N(C)C(OC(C)(C)C)=O)=O)OC VHNDAEBVQSXEQD-YRXYFLHQSA-N 0.000 description 1
- ZWGVITSIVJJNLB-JITSLDRASA-N CC(C(C(N(CC1)[C@H](Cc(c(ccc(F)c2)c2[nH]2)c2Cl)[C@H]1O)=O)NC(OC(C)(C)C)=O)OC Chemical compound CC(C(C(N(CC1)[C@H](Cc(c(ccc(F)c2)c2[nH]2)c2Cl)[C@H]1O)=O)NC(OC(C)(C)C)=O)OC ZWGVITSIVJJNLB-JITSLDRASA-N 0.000 description 1
- IYSQDNQWWNYPEZ-CABCVRRESA-N CC(C)(C)OC(N(CC1)[C@H](Cc(c(c([nH]2)c3)ccc3F)c2Cl)[C@H]1O)=O Chemical compound CC(C)(C)OC(N(CC1)[C@H](Cc(c(c([nH]2)c3)ccc3F)c2Cl)[C@H]1O)=O IYSQDNQWWNYPEZ-CABCVRRESA-N 0.000 description 1
- CSXNJPHCILPDOJ-TZHYSIJRSA-N CC(C)(C)OC(N(CC1)[C@H](Cc(c2ccccc2[nH]2)c2Br)C1OC(C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)[C@H](Cc(c2ccccc2[nH]2)c2Br)C1OC(C)=O)=O CSXNJPHCILPDOJ-TZHYSIJRSA-N 0.000 description 1
- RNDKWDBMRLWZAH-MSOLQXFVSA-N CC(C)(C)OC(N(CC1)[C@H](Cc2c[nH]c3cc(F)ccc23)[C@H]1OC(C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)[C@H](Cc2c[nH]c3cc(F)ccc23)[C@H]1OC(C)=O)=O RNDKWDBMRLWZAH-MSOLQXFVSA-N 0.000 description 1
- DUOPJIYJPLNLAJ-XCWJXAQQSA-N CC(C)(C)OC(N(CC1)[C@H](Cc2c[nH]c3ccccc23)C1/C=[O]/C(C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)[C@H](Cc2c[nH]c3ccccc23)C1/C=[O]/C(C)=O)=O DUOPJIYJPLNLAJ-XCWJXAQQSA-N 0.000 description 1
- PROGGNKQEKINHY-UHFFFAOYSA-N CC(C)(C)OC(NC(C1CCCCC1)C(N)=O)=O Chemical compound CC(C)(C)OC(NC(C1CCCCC1)C(N)=O)=O PROGGNKQEKINHY-UHFFFAOYSA-N 0.000 description 1
- QDRDGFLGLNXDSI-UHFFFAOYSA-N CC(C)C(C)(C=C)F Chemical compound CC(C)C(C)(C=C)F QDRDGFLGLNXDSI-UHFFFAOYSA-N 0.000 description 1
- PAIUHFOZOQRCOX-OSBQEZSISA-N CC(O[C@H](CC1)[C@@H](Cc(c2ccccc2[nH]2)c2Br)N1C(C(C1CCCCC1)N)=O)=O Chemical compound CC(O[C@H](CC1)[C@@H](Cc(c2ccccc2[nH]2)c2Br)N1C(C(C1CCCCC1)N)=O)=O PAIUHFOZOQRCOX-OSBQEZSISA-N 0.000 description 1
- DFZUWITUMOYLNP-UHFFFAOYSA-N CCc1cccnc1NC Chemical compound CCc1cccnc1NC DFZUWITUMOYLNP-UHFFFAOYSA-N 0.000 description 1
- YOJAHJGBFDPSDI-UHFFFAOYSA-N COC(c(cc1)ccc1[N+]([O-])=O)=O Chemical compound COC(c(cc1)ccc1[N+]([O-])=O)=O YOJAHJGBFDPSDI-UHFFFAOYSA-N 0.000 description 1
- CHHCOUQKDTZTQU-ZBHICJROSA-N C[C@@H]1C(NC=C)NC1 Chemical compound C[C@@H]1C(NC=C)NC1 CHHCOUQKDTZTQU-ZBHICJROSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- 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
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2323708P | 2008-01-24 | 2008-01-24 | |
| US61/023,237 | 2008-01-24 | ||
| PCT/US2009/031093 WO2009094287A1 (en) | 2008-01-24 | 2009-01-15 | Iap inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101951766A true CN101951766A (zh) | 2011-01-19 |
Family
ID=40901405
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980106206XA Pending CN101951766A (zh) | 2008-01-24 | 2009-01-15 | 凋亡抑制蛋白抑制剂 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20110288116A1 (enExample) |
| EP (1) | EP2242362A4 (enExample) |
| JP (1) | JP2011520770A (enExample) |
| KR (1) | KR20100119768A (enExample) |
| CN (1) | CN101951766A (enExample) |
| AU (1) | AU2009206588A1 (enExample) |
| BR (1) | BRPI0906785A2 (enExample) |
| CA (1) | CA2712604A1 (enExample) |
| IL (1) | IL207066A0 (enExample) |
| MX (1) | MX2010007948A (enExample) |
| WO (1) | WO2009094287A1 (enExample) |
| ZA (1) | ZA201005618B (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104870441A (zh) * | 2012-10-19 | 2015-08-26 | 阿斯特克斯治疗有限公司 | 双环杂环化合物及其治疗用途 |
| WO2019091492A1 (zh) * | 2017-11-13 | 2019-05-16 | 南京明德新药研发股份有限公司 | 用作iap抑制剂的smac模拟物及其用途 |
| WO2020177765A1 (zh) * | 2019-03-07 | 2020-09-10 | 正大天晴药业集团股份有限公司 | Iap抑制剂与免疫检查点抑制剂的组合 |
| WO2020228642A1 (zh) * | 2019-05-10 | 2020-11-19 | 正大天晴药业集团股份有限公司 | 一种用作iap抑制剂的smac模拟物的结晶及其制备方法 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8283372B2 (en) | 2009-07-02 | 2012-10-09 | Tetralogic Pharmaceuticals Corp. | 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic |
| WO2011075615A1 (en) | 2009-12-18 | 2011-06-23 | Idenix Pharmaceuticals, Inc. | 5,5-fused arylene or heteroarylene hepatitis c virus inhibitors |
| UY33236A (es) | 2010-02-25 | 2011-09-30 | Novartis Ag | Inhibidores dimericos de las iap |
| UY33794A (es) | 2010-12-13 | 2012-07-31 | Novartis Ag | Inhibidores diméricos de las iap |
| GB201106817D0 (en) | 2011-04-21 | 2011-06-01 | Astex Therapeutics Ltd | New compound |
| US20150190470A1 (en) * | 2012-08-01 | 2015-07-09 | Tetralogic Pharmaceuticals Corporation | Combination therapy |
| GB201218864D0 (en) | 2012-10-19 | 2012-12-05 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
| US9980973B2 (en) | 2012-10-19 | 2018-05-29 | Astex Therapeutics Limited | Bicyclic heterocycle compounds and their uses in therapy |
| GB201218850D0 (en) | 2012-10-19 | 2012-12-05 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
| LT3083616T (lt) | 2013-12-20 | 2021-09-10 | Astex Therapeutics Limited | Bicikinių heterociklų junginiai ir jų panaudojimas terapijoje |
| CA2974651A1 (en) | 2014-01-24 | 2015-07-30 | Children's Hospital Of Eastern Ontario Research Institute Inc. | Smc combination therapy for the treatment of cancer |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005069888A2 (en) * | 2004-01-16 | 2005-08-04 | The Regents Of The University Of Michigan | Smac peptidomimetics and the uses thereof |
| US20070203749A1 (en) * | 2005-08-09 | 2007-08-30 | Sri Chunduru | Business methods for compounds for treatment of proliferative disorders |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2253614B1 (en) * | 2004-04-07 | 2012-09-19 | Novartis AG | Inhibitors of IAP |
| WO2006010118A2 (en) * | 2004-07-09 | 2006-01-26 | The Regents Of The University Of Michigan | Conformationally constrained smac mimetics and the uses thereof |
| BRPI0607988A2 (pt) * | 2005-02-25 | 2009-10-27 | Tetralogic Pharmaceuticals | composto, composição farmacêutica, e método para induzir apoptose em uma célula |
-
2009
- 2009-01-15 CA CA2712604A patent/CA2712604A1/en not_active Abandoned
- 2009-01-15 KR KR1020107018102A patent/KR20100119768A/ko not_active Withdrawn
- 2009-01-15 WO PCT/US2009/031093 patent/WO2009094287A1/en not_active Ceased
- 2009-01-15 CN CN200980106206XA patent/CN101951766A/zh active Pending
- 2009-01-15 BR BRPI0906785-0A patent/BRPI0906785A2/pt not_active IP Right Cessation
- 2009-01-15 AU AU2009206588A patent/AU2009206588A1/en not_active Abandoned
- 2009-01-15 EP EP09703244A patent/EP2242362A4/en not_active Withdrawn
- 2009-01-15 JP JP2010544375A patent/JP2011520770A/ja not_active Abandoned
- 2009-01-15 MX MX2010007948A patent/MX2010007948A/es not_active Application Discontinuation
- 2009-01-15 US US12/863,375 patent/US20110288116A1/en not_active Abandoned
-
2010
- 2010-07-18 IL IL207066A patent/IL207066A0/en unknown
- 2010-08-05 ZA ZA2010/05618A patent/ZA201005618B/en unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005069888A2 (en) * | 2004-01-16 | 2005-08-04 | The Regents Of The University Of Michigan | Smac peptidomimetics and the uses thereof |
| US20070203749A1 (en) * | 2005-08-09 | 2007-08-30 | Sri Chunduru | Business methods for compounds for treatment of proliferative disorders |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104870441A (zh) * | 2012-10-19 | 2015-08-26 | 阿斯特克斯治疗有限公司 | 双环杂环化合物及其治疗用途 |
| CN104870441B (zh) * | 2012-10-19 | 2017-09-29 | 阿斯特克斯治疗有限公司 | 双环杂环化合物及其治疗用途 |
| US11358950B2 (en) | 2017-11-13 | 2022-06-14 | Chia Tai Tiangqing Pharmaceutical Group Co., Ltd. | SMAC mimetics used as IAP inhibitors and use thereof |
| CN111247161A (zh) * | 2017-11-13 | 2020-06-05 | 正大天晴药业集团股份有限公司 | 用作iap抑制剂的smac模拟物及其用途 |
| KR20200081456A (ko) * | 2017-11-13 | 2020-07-07 | 치아타이 티안큉 파마수티컬 그룹 주식회사 | Iap 억제제로서 유용한 smac 모방물 및 그 용도 |
| WO2019091492A1 (zh) * | 2017-11-13 | 2019-05-16 | 南京明德新药研发股份有限公司 | 用作iap抑制剂的smac模拟物及其用途 |
| AU2018364218B2 (en) * | 2017-11-13 | 2023-03-02 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | SMAC mimetics used as IAP inhibitors and use thereof |
| KR102707188B1 (ko) | 2017-11-13 | 2024-09-13 | 치아타이 티안큉 파마수티컬 그룹 주식회사 | Iap 억제제로서 유용한 smac 모방물 및 그 용도 |
| WO2020177765A1 (zh) * | 2019-03-07 | 2020-09-10 | 正大天晴药业集团股份有限公司 | Iap抑制剂与免疫检查点抑制剂的组合 |
| CN113677339A (zh) * | 2019-03-07 | 2021-11-19 | 正大天晴药业集团股份有限公司 | Iap抑制剂与免疫检查点抑制剂的组合 |
| CN113677339B (zh) * | 2019-03-07 | 2023-08-01 | 正大天晴药业集团股份有限公司 | Iap抑制剂与免疫检查点抑制剂的组合 |
| WO2020228642A1 (zh) * | 2019-05-10 | 2020-11-19 | 正大天晴药业集团股份有限公司 | 一种用作iap抑制剂的smac模拟物的结晶及其制备方法 |
| CN113748119A (zh) * | 2019-05-10 | 2021-12-03 | 正大天晴药业集团股份有限公司 | 一种用作iap抑制剂的smac模拟物的结晶及其制备方法 |
| CN113748119B (zh) * | 2019-05-10 | 2024-04-02 | 正大天晴药业集团股份有限公司 | 一种用作iap抑制剂的smac模拟物的结晶及其制备方法 |
| AU2020274768B2 (en) * | 2019-05-10 | 2025-06-26 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Crystalline form of smac mimic used as iap inhibitor and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| MX2010007948A (es) | 2010-10-04 |
| IL207066A0 (en) | 2010-12-30 |
| US20110288116A1 (en) | 2011-11-24 |
| CA2712604A1 (en) | 2009-07-30 |
| WO2009094287A1 (en) | 2009-07-30 |
| BRPI0906785A2 (pt) | 2015-07-14 |
| ZA201005618B (en) | 2011-04-28 |
| KR20100119768A (ko) | 2010-11-10 |
| JP2011520770A (ja) | 2011-07-21 |
| AU2009206588A1 (en) | 2009-07-30 |
| EP2242362A1 (en) | 2010-10-27 |
| EP2242362A4 (en) | 2012-04-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101951766A (zh) | 凋亡抑制蛋白抑制剂 | |
| AU2007276760B2 (en) | Dimeric IAP antagonists | |
| JP5452223B2 (ja) | Ｉａｐ阻害剤 | |
| JP5642777B2 (ja) | Ｉａｐ阻害剤 | |
| JP2012503004A (ja) | Ｉａｐ阻害剤 | |
| HK1204623A1 (en) | New phosphate compounds, a process for their preparation and pharmaceutical compositions containing them | |
| US9809574B2 (en) | Isoindoline or isoquinoline compounds, a process for their preparation and pharmaceutical compositions containing them | |
| CN101535300A (zh) | Iap bir域结合化合物 | |
| CN104854101A (zh) | Alk激酶抑制剂 | |
| CN105408321A (zh) | 新的吲哚和吡咯衍生物、它们的制备方法和含有它们的药物组合物 | |
| JP5631387B2 (ja) | Ｉａｐ阻害剤 | |
| CN114516873A (zh) | 一种螺环类化合物、包含其药物组合物及其应用 | |
| WO2011068926A1 (en) | Iap inhibitors | |
| CN119019362A (zh) | 杂芳环类化合物、其药物组合物及其应用 | |
| AU2012202098A1 (en) | Dimeric IAP antagonists |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20110119 |