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)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Rheumatology (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 |
| EP1183259A2 (de) * | 1999-09-28 | 2002-03-06 | Basf Aktiengesellschaft | Azepinoindol-derivate, deren herstellung und anwendung |
| DE19946289A1 (de) * | 1999-09-28 | 2001-03-29 | Basf Ag | Benzodiazepin-Derivate, deren Herstellung und Anwendung |
| 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 |
| WO2003103666A2 (en) * | 2002-06-07 | 2003-12-18 | Altana Pharma Ag | Novel 4,5-dihydro-imidazo[4,5,1-ij]quinolin-6-ones |
| JP3990718B2 (ja) | 2003-01-09 | 2007-10-17 | ファイザー・インク | キナーゼ阻害剤としてのジアゼピノインドール誘導体 |
| GB0305681D0 (en) | 2003-03-12 | 2003-04-16 | Kudos Pharm Ltd | Phthalazinone derivatives |
| US7449464B2 (en) | 2003-03-12 | 2008-11-11 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
| US7531530B2 (en) * | 2003-07-25 | 2009-05-12 | Cancer Research Technology Limited | Therapeutic compounds |
| 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 |
| PL2305221T3 (pl) * | 2003-12-01 | 2015-11-30 | Kudos Pharm Ltd | Inhibitory naprawy uszkodzeń DNA w leczeniu raka |
| GB0419072D0 (en) | 2004-08-26 | 2004-09-29 | Kudos Pharm Ltd | Phthalazinone derivatives |
| PT1794163E (pt) * | 2004-09-22 | 2010-03-01 | Pfizer | Método para a preparação de inibidores de poli(adpribose)- polimerases |
| US7820668B2 (en) * | 2005-01-19 | 2010-10-26 | Eisai Inc. | Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP |
| AR053902A1 (es) | 2005-06-14 | 2007-05-23 | Schering Corp | Inhibidores de aspartil proteasa heterociclicos macrociclicos |
| WO2006137510A1 (ja) | 2005-06-24 | 2006-12-28 | Ono Pharmaceutical Co., Ltd. | 脳血管障害時における出血低減剤 |
| ZA200800907B (en) * | 2005-07-18 | 2010-04-28 | Bipar Sciences Inc | Treatment of cancer |
| US20070032469A1 (en) * | 2005-08-05 | 2007-02-08 | Astrazeneca Ab | Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators |
| GB0521373D0 (en) | 2005-10-20 | 2005-11-30 | Kudos Pharm Ltd | Pthalazinone derivatives |
| JP2010504079A (ja) * | 2006-06-12 | 2010-02-12 | バイパー サイエンシズ,インコーポレイティド | Parp阻害剤を用いる疾病の治療方法 |
| US20100279327A1 (en) * | 2006-06-12 | 2010-11-04 | Bipar Sciences, Inc. | Method of treating diseases with parp inhibitors |
| US20080262062A1 (en) * | 2006-11-20 | 2008-10-23 | Bipar Sciences, Inc. | Method of treating diseases with parp inhibitors |
| CN101534836B (zh) * | 2006-09-05 | 2011-09-28 | 彼帕科学公司 | Parp抑制剂在制备治疗肥胖症的药物中的用途 |
| WO2008030883A2 (en) * | 2006-09-05 | 2008-03-13 | Bipar Sciences, Inc. | Treatment of cancer |
| 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. |
| EP2217244A4 (en) * | 2007-11-12 | 2011-08-31 | Bipar Sciences Inc | TREATMENT OF NUTRITIONAL CANCER AND EGG CANCER WITH A PARP INHIBITOR ALONE OR IN COMBINATION WITH ANTITUMOROUS MEDICINES |
| US7732491B2 (en) * | 2007-11-12 | 2010-06-08 | Bipar Sciences, Inc. | Treatment of breast cancer with a PARP inhibitor alone or in combination with anti-tumor agents |
| RU2010128107A (ru) * | 2007-12-07 | 2012-01-20 | Байпар Сайенсиз, Инк. (Us) | Лечение рака ингибиторами топоизомеразы в комбинации с ингибиторами parp |
| UY31603A1 (es) | 2008-01-23 | 2009-08-31 | Derivados de ftalazinona | |
| MX2010008572A (es) * | 2008-02-04 | 2010-11-30 | Bipar Sciences Inc | Metodos de diagnostico y tratamiento de enfermedades mediadas por poli(adp-ribosa) polimerasa. |
| GB0804755D0 (en) * | 2008-03-14 | 2008-04-16 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| CA2737400C (en) | 2008-10-07 | 2016-11-22 | Astrazeneca Uk Limited | Pharmaceutical formulation 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 |
| WO2014037313A1 (de) * | 2012-09-05 | 2014-03-13 | 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 |
| AU2016296905B2 (en) | 2015-07-23 | 2018-07-05 | Centre National De La Recherche Scientifique | Use of a combination of Dbait molecule and parp inhibitors to treat cancer |
| GB201519573D0 (en) | 2015-11-05 | 2015-12-23 | King S College London | Combination |
| WO2018022851A1 (en) | 2016-07-28 | 2018-02-01 | Mitobridge, Inc. | Methods of treating acute kidney injury |
| RU2019114863A (ru) | 2016-11-02 | 2020-12-03 | Иммуноджен, Инк. | Комбинированное лечение конъюгатами антитело-лекарственное средство и ингибиторами parp |
| 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 |
| CA3092779A1 (en) | 2018-03-13 | 2019-09-19 | Onxeo | A dbait molecule against acquired resistance in the treatment of cancer |
| US11535633B2 (en) | 2018-06-28 | 2022-12-27 | Jiangsu Hengrui Medicine Co., Ltd. | Fused tricyclic heterocycle compounds and therapeutic uses thereof |
| AU2019326633B2 (en) * | 2018-08-24 | 2022-09-08 | Adlai Nortye Biopharma Co., Ltd. | High activity sting protein agonist |
| US20220056044A1 (en) * | 2018-12-14 | 2022-02-24 | Jiangsu Hengrui Medicine Co., Ltd. | Tricyclic compounds as sting agonists, and preparation methods and medicinal uses thereof |
| CN113365998B (zh) * | 2019-02-02 | 2023-04-14 | 正大天晴药业集团股份有限公司 | 用于parp抑制剂的吲哚并七元酰肟类似物 |
| 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 |
| MX2022000449A (es) | 2019-07-10 | 2022-04-25 | Cybrexa 2 Inc | Conjugados peptídicos de citotoxinas como terapéuticos. |
| US11555019B2 (en) | 2019-07-10 | 2023-01-17 | Cybrexa 3, Inc. | Peptide conjugates of microtubule-targeting agents as therapeutics |
| GB201913030D0 (en) | 2019-09-10 | 2019-10-23 | Francis Crick Institute Ltd | Treatment of hr deficient cancer |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| US20230234938A1 (en) | 2020-04-28 | 2023-07-27 | Rhizen Pharmaceuticals Ag | Novel compounds useful as poly(adp-ribose) polymerase (parp) inhibitors |
| WO2022090938A1 (en) | 2020-10-31 | 2022-05-05 | Rhizen Pharmaceuticals Ag | Phthalazinone derivatives useful as parp inhibitors |
| CN116940691A (zh) | 2021-01-08 | 2023-10-24 | 赛博克萨2公司 | 用于制备缀合物连接部分的方法 |
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| US20250154115A1 (en) * | 2022-02-11 | 2025-05-15 | The University Of North Carolina At Chapel Hill | Arylbenzoisoxazole compounds as ip6k and ipmk inhibitors and methods of use thereof |
| CN121398822A (zh) | 2023-06-21 | 2026-01-23 | 四方生物科学有限公司 | 用于在治疗hr功能正常的癌症的方法中的用途的包含脱氧胞苷衍生物和parp抑制剂的组合 |
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