JP4272375B2 - ポリ(adp−リボース)ポリメラーゼの三環系阻害剤 - Google Patents
ポリ(adp−リボース)ポリメラーゼの三環系阻害剤 Download PDFInfo
- Publication number
- JP4272375B2 JP4272375B2 JP2001519702A JP2001519702A JP4272375B2 JP 4272375 B2 JP4272375 B2 JP 4272375B2 JP 2001519702 A JP2001519702 A JP 2001519702A JP 2001519702 A JP2001519702 A JP 2001519702A JP 4272375 B2 JP4272375 B2 JP 4272375B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- aryl
- heteroaryl
- heterocycloalkyl
- 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.)
- Expired - Lifetime
Links
- 0 *C(*)(*c1ccccc1*)C(*)(*)*I Chemical compound *C(*)(*c1ccccc1*)C(*)(*)*I 0.000 description 17
- KQOZQYFFMKFALA-UHFFFAOYSA-N CC(CNCc(cc1)ccc1C1=CCC(C)c2cccc3c2N1CCNC3=O)c1ccccc1 Chemical compound CC(CNCc(cc1)ccc1C1=CCC(C)c2cccc3c2N1CCNC3=O)c1ccccc1 KQOZQYFFMKFALA-UHFFFAOYSA-N 0.000 description 1
- XVFLDOZQTOHKLK-UHFFFAOYSA-N CCOC(c(cc1)ccc1-c1nc2cc(F)cc3c2[n]1CCNC3=O)OCC Chemical compound CCOC(c(cc1)ccc1-c1nc2cc(F)cc3c2[n]1CCNC3=O)OCC XVFLDOZQTOHKLK-UHFFFAOYSA-N 0.000 description 1
- GZVKGNVNVNJLAL-UHFFFAOYSA-N C[n]1nnc(-c(cc2)ccc2-c2nc3cccc4c3[n]2CCNC4=O)n1 Chemical compound C[n]1nnc(-c(cc2)ccc2-c2nc3cccc4c3[n]2CCNC4=O)n1 GZVKGNVNVNJLAL-UHFFFAOYSA-N 0.000 description 1
- FAZBAXPJGHTPQU-UHFFFAOYSA-N Cc(cc1)ccc1-c1nc(-c2nc3cccc4c3[n]2CCNC4=O)c[s]1 Chemical compound Cc(cc1)ccc1-c1nc(-c2nc3cccc4c3[n]2CCNC4=O)c[s]1 FAZBAXPJGHTPQU-UHFFFAOYSA-N 0.000 description 1
- ONMYBMWHNZHDJY-UHFFFAOYSA-N Cc1cccc2c1C1=NC1CCNC2=O Chemical compound Cc1cccc2c1C1=NC1CCNC2=O ONMYBMWHNZHDJY-UHFFFAOYSA-N 0.000 description 1
- VZLHOBQCHKAIOM-UHFFFAOYSA-N Cc1cccc2c1NCCC2=O Chemical compound Cc1cccc2c1NCCC2=O VZLHOBQCHKAIOM-UHFFFAOYSA-N 0.000 description 1
- RNVCVTLRINQCPJ-UHFFFAOYSA-N Cc1ccccc1N Chemical compound Cc1ccccc1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 1
- BYVZANXKKWSBJC-UHFFFAOYSA-N N#Cc(c1ccc2)c(-c(cc3)ccc3F)[n](CCN3)c1c2C3=O Chemical compound N#Cc(c1ccc2)c(-c(cc3)ccc3F)[n](CCN3)c1c2C3=O BYVZANXKKWSBJC-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N Nc(cccc1)c1N Chemical compound Nc(cccc1)c1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- DMUFLRSMPXULHE-UHFFFAOYSA-N Nc1cccc(C(NCCC2)=O)c1C2=N Chemical compound Nc1cccc(C(NCCC2)=O)c1C2=N DMUFLRSMPXULHE-UHFFFAOYSA-N 0.000 description 1
- XVHVPDMTBPMQAQ-UHFFFAOYSA-N Nc1cccc2c1NCCNC2=O Chemical compound Nc1cccc2c1NCCNC2=O XVHVPDMTBPMQAQ-UHFFFAOYSA-N 0.000 description 1
- OENJDOPFMDOTBV-GFCCVEGCSA-N O=C1NCCC[C@H]2C(c(cccc3)c3Cl)=Nc3cccc1c23 Chemical compound O=C1NCCC[C@H]2C(c(cccc3)c3Cl)=Nc3cccc1c23 OENJDOPFMDOTBV-GFCCVEGCSA-N 0.000 description 1
- RUYWJWDAXBXNSP-UHFFFAOYSA-N O=C1NCCNc2c1cccc2C#Cc(cc1)ccc1F Chemical compound O=C1NCCNc2c1cccc2C#Cc(cc1)ccc1F RUYWJWDAXBXNSP-UHFFFAOYSA-N 0.000 description 1
- XLFLIGQYRJBFHN-UHFFFAOYSA-N O=C1NCC[n]2c(-c(cc3)ccc3F)nc3cccc1c23 Chemical compound O=C1NCC[n]2c(-c(cc3)ccc3F)nc3cccc1c23 XLFLIGQYRJBFHN-UHFFFAOYSA-N 0.000 description 1
- XQAREQUPLFEKQN-UHFFFAOYSA-N O=C1NCC[n]2c(-c3ccc(CN4CC=CC4)cc3)nc3cccc1c23 Chemical compound O=C1NCC[n]2c(-c3ccc(CN4CC=CC4)cc3)nc3cccc1c23 XQAREQUPLFEKQN-UHFFFAOYSA-N 0.000 description 1
- SYMKFNGFZFMMLA-UHFFFAOYSA-N O=C1NCC[n]2c(-c3ccc(CNCc4ccccc4)cc3)nc3c2C1CC=C3 Chemical compound O=C1NCC[n]2c(-c3ccc(CNCc4ccccc4)cc3)nc3c2C1CC=C3 SYMKFNGFZFMMLA-UHFFFAOYSA-N 0.000 description 1
- FNVQPRGROKARAM-UHFFFAOYSA-N O=C1NCC[n]2c(-c3cccc(C4OCCCO4)c3)nc3cccc1c23 Chemical compound O=C1NCC[n]2c(-c3cccc(C4OCCCO4)c3)nc3cccc1c23 FNVQPRGROKARAM-UHFFFAOYSA-N 0.000 description 1
- UOCXKKNEJXCYOK-DAFODLJHSA-N O=CC(c1ccc2)=CC(/C=C/CCN3)c1c2C3=O Chemical compound O=CC(c1ccc2)=CC(/C=C/CCN3)c1c2C3=O UOCXKKNEJXCYOK-DAFODLJHSA-N 0.000 description 1
- NHTZRCULIGOJQB-UHFFFAOYSA-N OC1CN(Cc(cc2)ccc2-c2nc3cccc4c3[n]2CCNC4=O)CC1 Chemical compound OC1CN(Cc(cc2)ccc2-c2nc3cccc4c3[n]2CCNC4=O)CC1 NHTZRCULIGOJQB-UHFFFAOYSA-N 0.000 description 1
- RVAAOSVBOZQMOT-RJRFIUFISA-N OCC/C=C\c(c1ccc2)c(-c(cc3)ccc3F)[n](CCN3)c1c2C3=O Chemical compound OCC/C=C\c(c1ccc2)c(-c(cc3)ccc3F)[n](CCN3)c1c2C3=O RVAAOSVBOZQMOT-RJRFIUFISA-N 0.000 description 1
- RJPNRHSETMASQP-UHFFFAOYSA-N OCCNCc1ccc(C2(C(c3ccc4)=C2)N(CCN2)c3c4C2=O)cc1 Chemical compound OCCNCc1ccc(C2(C(c3ccc4)=C2)N(CCN2)c3c4C2=O)cc1 RJPNRHSETMASQP-UHFFFAOYSA-N 0.000 description 1
- AGSNQEIGQYAVST-KRWDZBQOSA-N OC[C@H]1N(Cc(cc2)ccc2-c2nc3cccc4c3[n]2CCNC4=O)CCC1 Chemical compound OC[C@H]1N(Cc(cc2)ccc2-c2nc3cccc4c3[n]2CCNC4=O)CCC1 AGSNQEIGQYAVST-KRWDZBQOSA-N 0.000 description 1
- FVLNAXKAAQUKBA-UHFFFAOYSA-N OCc(cc1)ccc1-c1nc2cc(F)cc3c2[n]1CCNC3=O Chemical compound OCc(cc1)ccc1-c1nc2cc(F)cc3c2[n]1CCNC3=O FVLNAXKAAQUKBA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D487/06—Peri-condensed systems
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15214299P | 1999-08-31 | 1999-08-31 | |
| US60/152,142 | 1999-08-31 | ||
| PCT/US2000/023882 WO2001016136A2 (en) | 1999-08-31 | 2000-08-31 | Tricyclic inhibitors of poly(adp-ribose) polymerases |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003513015A JP2003513015A (ja) | 2003-04-08 |
| JP2003513015A5 JP2003513015A5 (https=) | 2006-09-21 |
| JP4272375B2 true JP4272375B2 (ja) | 2009-06-03 |
Family
ID=22541675
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001519702A Expired - Lifetime JP4272375B2 (ja) | 1999-08-31 | 2000-08-31 | ポリ(adp−リボース)ポリメラーゼの三環系阻害剤 |
Country Status (48)
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6291425B1 (en) | 1999-09-01 | 2001-09-18 | Guilford Pharmaceuticals Inc. | Compounds, methods and pharmaceutical compositions for treating cellular damage, such as neural or cardiovascular tissue damage |
| DE19946289A1 (de) * | 1999-09-28 | 2001-03-29 | Basf Ag | Benzodiazepin-Derivate, deren Herstellung und Anwendung |
| KR20010087401A (ko) * | 1999-09-28 | 2001-09-15 | 스타르크, 카르크 | 아제피노인돌 유도체, 그의 제법 및 용도 |
| DE10021468A1 (de) * | 2000-05-04 | 2001-11-08 | Basf Ag | Verwendung von PARP-Inhibitoren in kosmetischen Zubereitungen |
| US7151102B2 (en) | 2000-10-30 | 2006-12-19 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
| FR2816942B1 (fr) * | 2000-11-23 | 2003-05-09 | Sanofi Synthelabo | Derives de benzimidazole, leur preparation et leur application en therapeutique |
| WO2003051879A1 (en) * | 2001-12-14 | 2003-06-26 | Altana Pharma Ag | Known and novel 4,5-dihydro-imidazo[4,5,1-ij]quinolin-6-ones useful as poly(adp-ribose)polymerase inhibitors |
| US7026311B2 (en) | 2002-01-10 | 2006-04-11 | Abbott Gmbh & Co., Kg | Dibenzodiazepine derivatives, their preparation and use |
| DE60335359D1 (de) | 2002-04-30 | 2011-01-27 | Kudos Pharm Ltd | Phthalazinonderivate |
| AU2003236686A1 (en) * | 2002-06-07 | 2003-12-22 | Altana Pharma Ag | 4,5-dihydro-imidazo(4,5,1-j) quinolin-6-ones as parp inhibitors |
| CA2512683C (en) | 2003-01-09 | 2010-03-16 | Pfizer Inc. | Tricyclic compounds protein kinase inhibitors for enhancing the efficacy of anti-neoplastic agents and radiation therapy |
| US7449464B2 (en) | 2003-03-12 | 2008-11-11 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
| GB0305681D0 (en) | 2003-03-12 | 2003-04-16 | Kudos Pharm Ltd | Phthalazinone derivatives |
| SI1660095T1 (sl) | 2003-07-25 | 2010-05-31 | Cancer Rec Tech Ltd | Triciklični parp inhibitorji |
| GB0317466D0 (en) * | 2003-07-25 | 2003-08-27 | Univ Sheffield | Use |
| WO2005035534A1 (ja) * | 2003-10-08 | 2005-04-21 | Ono Pharmaceutical Co., Ltd. | 複素ビシクロ環および複素トリシクロ環化合物およびその医薬 |
| KR20060123403A (ko) | 2003-12-01 | 2006-12-01 | 쿠도스 파마슈티칼스 리미티드 | 암 치료를 위한 dna 손상 수복 억제제 |
| GB0419072D0 (en) | 2004-08-26 | 2004-09-29 | Kudos Pharm Ltd | Phthalazinone derivatives |
| DK1794163T3 (da) * | 2004-09-22 | 2010-04-12 | Pfizer | Fremgangsmåde til fremstilling af poly(ADP-ribose)polymeraseinhibitorer |
| WO2006078711A2 (en) * | 2005-01-19 | 2006-07-27 | Mgi Gp, Inc. | Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting parp |
| CA2609562A1 (en) | 2005-06-14 | 2006-12-28 | Schering Corporation | Macrocyclic heterocyclic aspartyl protease inhibitors |
| US20090226412A1 (en) | 2005-06-24 | 2009-09-10 | Ono Pharmaceutical Co., Ltd., | Agent for reduction of bleeding in cerebrovascular disorder |
| CA2615374A1 (en) * | 2005-07-18 | 2007-01-25 | Ernest Kun Kun | Treatment of cancer |
| KR20080035576A (ko) * | 2005-08-05 | 2008-04-23 | 아스트라제네카 아베 | 트리사이클릭 벤즈이미다졸 및 대사체 글루타메이트 수용체조절제로서 이들의 용도 |
| GB0521373D0 (en) | 2005-10-20 | 2005-11-30 | Kudos Pharm Ltd | Pthalazinone derivatives |
| US20080262062A1 (en) * | 2006-11-20 | 2008-10-23 | Bipar Sciences, Inc. | Method of treating diseases with parp inhibitors |
| WO2008147418A1 (en) * | 2006-06-12 | 2008-12-04 | Bipar Sciences, Inc. | Method of treating diseases with parp inhibitors |
| US20100279327A1 (en) * | 2006-06-12 | 2010-11-04 | Bipar Sciences, Inc. | Method of treating diseases with parp inhibitors |
| CA2662337A1 (en) * | 2006-09-05 | 2008-03-13 | Bipar Sciences, Inc. | Inhibition of fatty acid synthesis by parp inhibitors and methods of treatment thereof |
| JP2010502730A (ja) * | 2006-09-05 | 2010-01-28 | バイパー サイエンシズ,インコーポレイティド | 癌の治療法 |
| UY30639A1 (es) | 2006-10-17 | 2008-05-31 | Kudos Pharm Ltd | Derivados sustituidos de 2h-ftalazin-1-ona, sus formas cristalinas, proceso de preparacion y aplicaciones |
| AU2008258599B2 (en) | 2007-06-05 | 2013-06-13 | Nsab, Filial Af Neurosearch Sweden Ab, Sverige | Disubstituted phenylpyrrolidines as modulators of cortical catecholaminergic neurotransmission |
| WO2008154129A1 (en) * | 2007-06-08 | 2008-12-18 | Bausch & Lomb Incorporated | Pharmaceutical compositions and method for treating, reducing, ameliorating, alleviating, or preventing dry eye |
| MX2010002749A (es) | 2007-09-14 | 2010-06-25 | Astrazeneca Ab | Derivados de ftalazinona. |
| CN103169973A (zh) * | 2007-11-12 | 2013-06-26 | 彼帕科学公司 | 使用4-碘-3-硝基苯甲酰胺化合物与抗肿瘤剂组合治疗乳腺癌 |
| KR20100102607A (ko) * | 2007-11-12 | 2010-09-24 | 바이파 사이언스 인코포레이티드 | Parp 억제제를 단독으로 사용하거나 항종양제와 병용하여 자궁암 및 난소암을 치료하는 방법 |
| CA2708157A1 (en) * | 2007-12-07 | 2009-06-11 | Bipar Sciences, Inc. | Treatment of cancer with combinations of topoisomerase inhibitors and parp inhibitors |
| AR070221A1 (es) | 2008-01-23 | 2010-03-25 | Astrazeneca Ab | Derivados de ftalazinona inhibidores de polimerasas, composiciones farmaceuticas que los contienen y usos de los mismos para prevenir y/o tratar tumores cancerigenos,lesiones isquemicas y otras enfermedades asociadas. |
| CA2713156A1 (en) * | 2008-02-04 | 2009-08-13 | Bipar Sciences, Inc. | Methods of diagnosing and treating parp-mediated diseases |
| GB0804755D0 (en) * | 2008-03-14 | 2008-04-16 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| ES2598178T5 (es) | 2008-10-07 | 2023-12-26 | Kudos Pharm Ltd | Formulación farmacéutica 514 |
| WO2011058367A2 (en) | 2009-11-13 | 2011-05-19 | Astrazeneca Ab | Diagnostic test for predicting responsiveness to treatment with poly(adp-ribose) polymerase (parp) inhibitor |
| EP2892344A1 (de) * | 2012-09-05 | 2015-07-15 | Bayer CropScience AG | Verwendung substituierter benzodiazepinone und benzazepinone oder deren salze als wirkstoffe gegen abiotischen pflanzenstress |
| CA2935857C (en) * | 2014-01-05 | 2020-12-15 | Washington University | Radiolabeled tracers for poly (adp-ribose) polymerase-1 (parp-1), methods and uses therefor |
| JP6457696B2 (ja) | 2015-07-23 | 2019-01-23 | アンスティテュ・キュリInstitut Curie | 癌を処置するためのDbait分子とPARPインヒビターとの組合せの使用 |
| GB201519573D0 (en) | 2015-11-05 | 2015-12-23 | King S College London | Combination |
| US10874641B2 (en) | 2016-07-28 | 2020-12-29 | Mitobridge, Inc. | Methods of treating acute kidney injury |
| AU2017355402A1 (en) | 2016-11-02 | 2019-05-30 | Health Research, Inc. | Combination treatment with antibody-drug conjugates and PARP inhibitors |
| WO2018162439A1 (en) | 2017-03-08 | 2018-09-13 | Onxeo | New predictive biomarker for the sensitivity to a treatment of cancer with a dbait molecule |
| WO2018197461A1 (en) | 2017-04-28 | 2018-11-01 | Akribes Biomedical Gmbh | A parp inhibitor in combination with a glucocorticoid and/or ascorbic acid and/or a protein growth factor for the treatment of impaired wound healing |
| KR20200121800A (ko) | 2018-01-05 | 2020-10-26 | 싸이브렉사 1, 인크. | 산성 또는 저산소성 질환에 걸린 조직에 관련된 질환의 치료를 위한 화합물, 조성물 및 방법 |
| KR20200130856A (ko) | 2018-03-13 | 2020-11-20 | 옹쎄오 | 암 치료에서 획득한 내성에 대한 디베이트 분자 |
| JP2021530442A (ja) * | 2018-06-28 | 2021-11-11 | ジエンス ヘンルイ メデイシンカンパニー リミテッドJiangsu Hengrui Medicine Co., Ltd. | 縮合三環系複素環化合物およびその治療上の使用 |
| JP7584802B2 (ja) * | 2018-08-24 | 2024-11-18 | アドライ・ノーティ・バイオファーマ・カンパニー・リミテッド | 高活性stingタンパク質アゴニスト |
| WO2020124059A1 (en) * | 2018-12-14 | 2020-06-18 | Eternity Bioscience Inc. | Tricyclic compounds as sting agonists, and preparation methods and medicinal uses thereof |
| SG11202108399PA (en) * | 2019-02-02 | 2021-09-29 | Chia Tai Tianqing Pharmaceutical Group Co Ltd | Indolo heptamyl oxime analogue as parp inhibitor |
| CN111909157B (zh) * | 2019-05-07 | 2023-02-03 | 南京药石科技股份有限公司 | Ezh2抑制剂及其用途 |
| TW202116356A (zh) | 2019-07-10 | 2021-05-01 | 美商斯布雷克薩三號公司 | 作為治療劑之微管靶向藥劑之肽結合物 |
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