CN105492429A - Sumo活化酶的杂芳基抑制剂 - Google Patents
Sumo活化酶的杂芳基抑制剂 Download PDFInfo
- Publication number
- CN105492429A CN105492429A CN201480046426.9A CN201480046426A CN105492429A CN 105492429 A CN105492429 A CN 105492429A CN 201480046426 A CN201480046426 A CN 201480046426A CN 105492429 A CN105492429 A CN 105492429A
- Authority
- CN
- China
- Prior art keywords
- amino
- carbonyl
- methyl ester
- sulfamic acid
- pyrimidin
- 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 CC(*)(CC(COS(N)(=O)=O)C1)C1N(*)c1ncnc(*)c1C(C(C(*)=C(*)N*(C1)(C2C1(*)*2[Re])[Re])=*)=O Chemical compound CC(*)(CC(COS(N)(=O)=O)C1)C1N(*)c1ncnc(*)c1C(C(C(*)=C(*)N*(C1)(C2C1(*)*2[Re])[Re])=*)=O 0.000 description 13
- UYNOXTHSDFPJQC-UHFFFAOYSA-N C=NNCc1cccc(Cl)c1 Chemical compound C=NNCc1cccc(Cl)c1 UYNOXTHSDFPJQC-UHFFFAOYSA-N 0.000 description 2
- JZQLJHIDFDVMDY-UHFFFAOYSA-N C/[I]=C(\CCN)/CO Chemical compound C/[I]=C(\CCN)/CO JZQLJHIDFDVMDY-UHFFFAOYSA-N 0.000 description 1
- FUPCHIJVCBGZEK-JWWFHCCTSA-N CC(Cc1cncnc1N[C@@H](C[C@@H]1OC(C)(C)O)CC1(C1)C1=O)[OH3+2] Chemical compound CC(Cc1cncnc1N[C@@H](C[C@@H]1OC(C)(C)O)CC1(C1)C1=O)[OH3+2] FUPCHIJVCBGZEK-JWWFHCCTSA-N 0.000 description 1
- MWOVFCCILWBHLM-UHFFFAOYSA-N CC1(C)OB(C=C)OC1 Chemical compound CC1(C)OB(C=C)OC1 MWOVFCCILWBHLM-UHFFFAOYSA-N 0.000 description 1
- FLXMCYGUCUWNSA-QPJJXVBHSA-N CCC(C)/C=C(/N=C\N)\Cl Chemical compound CCC(C)/C=C(/N=C\N)\Cl FLXMCYGUCUWNSA-QPJJXVBHSA-N 0.000 description 1
- CZJHCMBIBAZWCE-JAMMHHFISA-N C[C@@H](CCC=N1)C(C)C=C1Cl Chemical compound C[C@@H](CCC=N1)C(C)C=C1Cl CZJHCMBIBAZWCE-JAMMHHFISA-N 0.000 description 1
- XJPZKYIHCLDXST-UHFFFAOYSA-N Clc1ncnc(Cl)c1 Chemical compound Clc1ncnc(Cl)c1 XJPZKYIHCLDXST-UHFFFAOYSA-N 0.000 description 1
- MXOIIXRYAPGBEN-CKRUTQJISA-N NS(CC[C@@H](C[C@H](C1)Nc2ncnc(Cl)c2C(c2n[n](Cc3cccc(Cl)c3)cc2)=O)[C@H]1O)(=O)=[U] Chemical compound NS(CC[C@@H](C[C@H](C1)Nc2ncnc(Cl)c2C(c2n[n](Cc3cccc(Cl)c3)cc2)=O)[C@H]1O)(=O)=[U] MXOIIXRYAPGBEN-CKRUTQJISA-N 0.000 description 1
- ROQIWOPSUUICIF-UHFFFAOYSA-N O=Cc1n[n](Cc2cccc(Cl)c2)cc1 Chemical compound O=Cc1n[n](Cc2cccc(Cl)c2)cc1 ROQIWOPSUUICIF-UHFFFAOYSA-N 0.000 description 1
- AESIVDWDYMOZGZ-UHFFFAOYSA-N OC1(COC1)C#CCBr Chemical compound OC1(COC1)C#CCBr AESIVDWDYMOZGZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- 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
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361842097P | 2013-07-02 | 2013-07-02 | |
| US61/842,097 | 2013-07-02 | ||
| PCT/US2014/045129 WO2015002994A2 (en) | 2013-07-02 | 2014-07-01 | Heteroaryl compounds useful as inhibitors of sumo activating enzyme |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105492429A true CN105492429A (zh) | 2016-04-13 |
Family
ID=52144279
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480046426.9A Pending CN105492429A (zh) | 2013-07-02 | 2014-07-01 | Sumo活化酶的杂芳基抑制剂 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9695154B2 (enExample) |
| EP (1) | EP3016934B1 (enExample) |
| JP (1) | JP6378759B2 (enExample) |
| CN (1) | CN105492429A (enExample) |
| BR (1) | BR112015032902A8 (enExample) |
| CA (1) | CA2916468C (enExample) |
| EA (1) | EA032577B1 (enExample) |
| WO (1) | WO2015002994A2 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105670066A (zh) * | 2016-04-22 | 2016-06-15 | 宁波硫华聚合物有限公司 | 橡胶促进剂活性剂氧化镁母胶粒及其制备方法 |
| CN107586315A (zh) * | 2016-07-08 | 2018-01-16 | 成都海创药业有限公司 | 一种嵌合分子 |
| WO2024067676A1 (zh) * | 2022-09-30 | 2024-04-04 | 微境生物医药科技(上海)有限公司 | 作为sumo活化酶抑制剂的化合物 |
| WO2024099438A1 (zh) * | 2022-11-11 | 2024-05-16 | 微境生物医药科技(上海)有限公司 | 作为sumo活化酶抑制剂的化合物 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8008307B2 (en) | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| US9290500B2 (en) | 2012-02-17 | 2016-03-22 | Millennium Pharmaceuticals, Inc. | Pyrazolopyrimidinyl inhibitors of ubiquitin-activating enzyme |
| WO2014022744A1 (en) | 2012-08-03 | 2014-02-06 | Millennium Pharmaceuticals, Inc. | INDOLE-SUBSTITUTED PYRROLOPYRIMIDINYL INHIBITORS OF Uba6 |
| US9695154B2 (en) | 2013-07-02 | 2017-07-04 | Millennium Pharmaceuticals, Inc. | Heteroaryl inhibitors of sumo activating enzyme |
| PT3164130T (pt) * | 2014-07-01 | 2019-11-18 | Millennium Pharm Inc | Compostos de heteroaril úteis como inibidores de enzima ativadora de sumo |
| WO2017183927A1 (ko) * | 2016-04-20 | 2017-10-26 | 한국화학연구원 | 신규한 헤테로고리 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물 |
| US10875834B2 (en) | 2016-07-22 | 2020-12-29 | Virginia Commonwealth University | Prodrug and protected forms of 5-hydroxymethylfurfuranal (5-HMF) and its derivatives |
| EP3820475A4 (en) | 2018-07-09 | 2022-04-13 | Takeda Pharmaceutical Company Limited | Administration of sumo-activating enzyme inhibitor and anti-cd20 antibodies |
| JP7394831B2 (ja) * | 2018-07-27 | 2023-12-08 | アーカス バイオサイエンシズ インコーポレイティド | ピリドンａ２ｒアンタゴニスト |
| WO2020028525A1 (en) * | 2018-07-31 | 2020-02-06 | City Of Hope | Sumo inhibitor compounds and uses thereof |
| KR20210131316A (ko) | 2019-02-27 | 2021-11-02 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | Sumo-활성화 효소 저해제 및 관문 저해제의 투여 |
| WO2022159980A1 (en) * | 2021-01-25 | 2022-07-28 | Athos Therapeutics, Inc. | Pharmaceutical compounds and methods of making and using the same |
| WO2023073645A1 (en) | 2021-10-29 | 2023-05-04 | Takeda Pharmaceutical Company Limited | Therapy comprising anti-cd19 antibody and sumo-activating enzyme inhibitor |
| WO2024097736A1 (en) * | 2022-11-02 | 2024-05-10 | Arcus Biosciences, Inc. | Processes for preparing azolopyrimidine compounds |
| CN116640068A (zh) * | 2023-05-26 | 2023-08-25 | 康化（上海）新药研发有限公司 | 一种（3-环丙基-2-炔-1-基）甘氨酸苄酯的合成方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101516850A (zh) * | 2006-08-08 | 2009-08-26 | 米伦纽姆医药公司 | 适用作e1活化酶抑制剂的杂芳基化合物 |
| US20120258927A1 (en) * | 2006-02-02 | 2012-10-11 | Millenium Pharmaceuticals, Inc. | Inhibitors of e1 activating enzymes |
| US20130150388A1 (en) * | 2011-08-24 | 2013-06-13 | Millennium Pharmaceuticals, Inc. | Inhibitors of nedd8-activating enzyme |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5194446A (en) | 1989-06-12 | 1993-03-16 | A. H. Robins Company, Incorporated | Compounds having one or more aminosulfaonyloxy radicals useful as pharmaceuticals |
| AU6500696A (en) | 1995-07-28 | 1997-02-26 | Cubist Pharmaceuticals, Inc. | Aminoacyl adenylate mimics as novel antimicrobial and antiparasitic agents |
| JP2005524662A (ja) | 2002-02-28 | 2005-08-18 | ビオタ インコーポレーティッド | ヌクレオシド５’−一リン酸模倣物およびこれらのプロドラッグ |
| US7291603B2 (en) | 2002-07-24 | 2007-11-06 | Ptc Therapeutics, Inc. | Nucleoside compounds and their use for treating cancer and diseases associated with somatic mutations |
| CA2493816A1 (en) | 2002-07-24 | 2004-01-29 | Ptc Therapeutics, Inc. | Use of nucleoside compounds for nonsense suppression and the treatment of genetic diseases |
| ATE364608T1 (de) | 2002-09-04 | 2007-07-15 | Schering Corp | Pyrazolopyrimidine als hemmstoffe cyclin- abhängiger kinasen |
| NZ539161A (en) | 2002-09-04 | 2006-05-26 | Schering Corp | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7563798B2 (en) | 2002-09-04 | 2009-07-21 | Schering Corporation | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| US7196092B2 (en) | 2002-09-04 | 2007-03-27 | Schering Corporation | N-heteroaryl pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| WO2004043955A1 (en) | 2002-11-13 | 2004-05-27 | Rigel Pharmaceuticals, Inc. | Rhodanine derivatives and pharmaceutical compositions containing them |
| US20070179161A1 (en) | 2003-03-31 | 2007-08-02 | Vernalis (Cambridge) Limited. | Pyrazolopyrimidine compounds and their use in medicine |
| JP2005008581A (ja) | 2003-06-20 | 2005-01-13 | Kissei Pharmaceut Co Ltd | 新規なピラゾロ［１，５−ａ］ピリミジン誘導体、それを含有する医薬組成物およびそれらの用途 |
| EP1680431A1 (en) | 2003-10-17 | 2006-07-19 | Rigel Pharmaceuticals, Inc. | Benzothiazole and thiazole'5,5-b!pyridine compositions and their use as ubiquitin ligase inhibitors |
| US20070105890A1 (en) | 2003-11-26 | 2007-05-10 | Dainippon Sumitomo Pharma Co., Ltd | Novel condensed imidazole derivative |
| US20050282818A1 (en) | 2004-06-22 | 2005-12-22 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase inhibitors |
| CA2596424C (en) | 2005-02-04 | 2016-03-29 | Millennium Pharmaceuticals, Inc. | Inhibitors of e1 activating enzymes |
| WO2007044426A2 (en) | 2005-10-06 | 2007-04-19 | Schering Corporation | Pyrazolopyrimidines as protein kinase inhibitors |
| US8008307B2 (en) | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| TW201716375A (zh) | 2007-06-12 | 2017-05-16 | Achaogen Inc | 抗菌劑 |
| US9216983B2 (en) | 2007-12-21 | 2015-12-22 | Board Of Regents, University Of Texas System | Dihydroorotate dehydrogenase inhibitors with selective anti-malarial activity |
| US8541434B2 (en) | 2008-08-20 | 2013-09-24 | Merck Sharp & Dohme Corp. | Ethynyl-substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
| WO2010022121A1 (en) | 2008-08-20 | 2010-02-25 | Schering Corporation | Substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
| US8470834B2 (en) | 2008-08-20 | 2013-06-25 | Merck Sharp & Dohme Corp. | AZO-substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
| JP5619743B2 (ja) | 2008-08-20 | 2014-11-05 | メルク・シャープ・アンド・ドーム・コーポレーションＭｅｒｃｋ Ｓｈａｒｐ ＆ Ｄｏｈｍｅ Ｃｏｒｐ． | エテニル置換ピリジンおよびピリミジン誘導体およびウイルス感染の治療におけるそれらの使用 |
| AU2009298802A1 (en) | 2008-09-23 | 2010-04-08 | Alnylam Pharmaceuticals, Inc. | Chemical modifications of monomers and oligonucleotides with cycloaddition |
| WO2010086040A1 (en) | 2009-01-29 | 2010-08-05 | Biomarin Iga, Ltd. | Pyrazolo-pyrimidines for treatment of duchenne muscular dystrophy |
| WO2010088518A2 (en) | 2009-01-31 | 2010-08-05 | Kalypsys, Inc. | Heterocyclic modulators of gpr119 for treatment of disease |
| KR20120024715A (ko) | 2009-05-14 | 2012-03-14 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | （（1ｓ，2ｓ，4ｒ）?4?｛4?〔（1ｓ)?2，3?디하이드로?1ｈ?인덴?1?일아미노〕?7ｈ?피롤로〔2，3?ｄ〕피리미딘?7?일｝?2?하이드록시사이클로펜틸)메틸 설파메이트의 하이드로클로라이드 염 |
| EP3205647B1 (en) | 2009-08-17 | 2020-05-13 | Memorial Sloan-Kettering Cancer Center | 2-(pyrimidin-5-yl)-thiopyrimidine derivatives as hsp70 and hsc70 modulators for the treatment of proliferative disorders |
| US9198972B2 (en) | 2010-01-28 | 2015-12-01 | Alnylam Pharmaceuticals, Inc. | Monomers and oligonucleotides comprising cycloaddition adduct(s) |
| EP2536410B1 (en) | 2010-02-18 | 2015-09-23 | Merck Sharp & Dohme Corp. | Substituted pyrimidine derivatives and their use in treating viral infections |
| WO2011109059A1 (en) | 2010-03-01 | 2011-09-09 | Gtx, Inc. | Compounds for treatment of cancer |
| ES2823350T3 (es) | 2010-07-29 | 2021-05-06 | Rigel Pharmaceuticals Inc | Compuestos heterocíclicos que activan AMPK y métodos de uso de los mismos |
| US20120077814A1 (en) | 2010-09-10 | 2012-03-29 | Zhong Wang | Sulfonamide, sulfamate, and sulfamothioate derivatives |
| JP2015502137A (ja) * | 2011-10-07 | 2015-01-22 | ミレニアム ファーマシューティカルズ， インコーポレイテッドＭｉｌｌｅｎｎｉｕｍ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． | Ｅ１酵素変異体およびその用途 |
| EP2773207B1 (en) | 2011-10-31 | 2018-03-07 | Merck Sharp & Dohme Corp. | Aminopyrimidinones as interleukin receptor-associated kinase inhibitors |
| US9290500B2 (en) | 2012-02-17 | 2016-03-22 | Millennium Pharmaceuticals, Inc. | Pyrazolopyrimidinyl inhibitors of ubiquitin-activating enzyme |
| WO2013151975A1 (en) | 2012-04-02 | 2013-10-10 | Northeastern University | Compositions and methods for the inhibition of methyltransferases |
| US9695154B2 (en) | 2013-07-02 | 2017-07-04 | Millennium Pharmaceuticals, Inc. | Heteroaryl inhibitors of sumo activating enzyme |
| WO2015048547A2 (en) | 2013-09-26 | 2015-04-02 | Rigel Pharmaceuticals, Inc. | Methods for using and biomarkers for ampk-activating compounds |
| EP3060550B1 (en) | 2013-10-21 | 2019-05-15 | Merck Patent GmbH | Heteroaryl compounds as btk inhibitors and uses thereof |
| WO2015110999A1 (en) | 2014-01-24 | 2015-07-30 | Piramal Enterprises Limited | Ezh2 inhibitors and uses thereof |
-
2014
- 2014-07-01 US US14/901,809 patent/US9695154B2/en active Active
- 2014-07-01 EA EA201690129A patent/EA032577B1/ru not_active IP Right Cessation
- 2014-07-01 WO PCT/US2014/045129 patent/WO2015002994A2/en not_active Ceased
- 2014-07-01 JP JP2016524326A patent/JP6378759B2/ja not_active Expired - Fee Related
- 2014-07-01 CA CA2916468A patent/CA2916468C/en not_active Expired - Fee Related
- 2014-07-01 CN CN201480046426.9A patent/CN105492429A/zh active Pending
- 2014-07-01 BR BR112015032902A patent/BR112015032902A8/pt not_active Application Discontinuation
- 2014-07-01 EP EP14819587.8A patent/EP3016934B1/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20120258927A1 (en) * | 2006-02-02 | 2012-10-11 | Millenium Pharmaceuticals, Inc. | Inhibitors of e1 activating enzymes |
| CN101516850A (zh) * | 2006-08-08 | 2009-08-26 | 米伦纽姆医药公司 | 适用作e1活化酶抑制剂的杂芳基化合物 |
| US20130150388A1 (en) * | 2011-08-24 | 2013-06-13 | Millennium Pharmaceuticals, Inc. | Inhibitors of nedd8-activating enzyme |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105670066A (zh) * | 2016-04-22 | 2016-06-15 | 宁波硫华聚合物有限公司 | 橡胶促进剂活性剂氧化镁母胶粒及其制备方法 |
| CN107586315A (zh) * | 2016-07-08 | 2018-01-16 | 成都海创药业有限公司 | 一种嵌合分子 |
| CN107586315B (zh) * | 2016-07-08 | 2020-03-31 | 成都海创药业有限公司 | 一种嵌合分子 |
| WO2024067676A1 (zh) * | 2022-09-30 | 2024-04-04 | 微境生物医药科技(上海)有限公司 | 作为sumo活化酶抑制剂的化合物 |
| WO2024099438A1 (zh) * | 2022-11-11 | 2024-05-16 | 微境生物医药科技(上海)有限公司 | 作为sumo活化酶抑制剂的化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EA201690129A1 (ru) | 2016-06-30 |
| JP6378759B2 (ja) | 2018-08-22 |
| EP3016934A2 (en) | 2016-05-11 |
| CA2916468A1 (en) | 2015-01-08 |
| EP3016934B1 (en) | 2018-01-10 |
| EA032577B1 (ru) | 2019-06-28 |
| US9695154B2 (en) | 2017-07-04 |
| JP2016523925A (ja) | 2016-08-12 |
| EP3016934A4 (en) | 2016-12-14 |
| WO2015002994A2 (en) | 2015-01-08 |
| US20160355504A1 (en) | 2016-12-08 |
| BR112015032902A8 (pt) | 2019-12-24 |
| CA2916468C (en) | 2019-07-23 |
| WO2015002994A3 (en) | 2015-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20230293522A1 (en) | Heteroaryl compounds useful as inhibitors of sumo activating enzyme | |
| CN105492429A (zh) | Sumo活化酶的杂芳基抑制剂 | |
| JP7550870B2 (ja) | Ｙａｐ／ｔａｚ－ｔｅａｄタンパク質－タンパク質相互作用阻害剤としてのビアリール誘導体 | |
| CN112105385A (zh) | Irak降解剂和其用途 | |
| JP2019081786A (ja) | Ｔｒｋａキナーゼ阻害剤としてのｎ−ピロリジニル、ｎ’−ピラゾリル尿素、チオ尿素、グアニジン、およびシアノグアニジン化合物 | |
| EP2976341B1 (en) | Acyclic cyanoethylpyrazolo pyridones as janus kinase inhibitors | |
| TW201249842A (en) | Dispiropyrrolidine derivatives | |
| CN112135818A (zh) | 4-羟基哌啶衍生物及其作为泛素特异性蛋白酶19(usp19)的抑制剂的用途 | |
| WO2007020936A1 (ja) | 抗真菌作用二環性複素環化合物 | |
| TW202448473A (zh) | 包含ｓｏｓ１抑制劑及抗癌藥物的用於治療癌症之藥學組成物 | |
| JP2025518041A (ja) | ヘテロ環のｐａｄ４阻害剤 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| AD01 | Patent right deemed abandoned |
Effective date of abandoning: 20200211 |
|
| AD01 | Patent right deemed abandoned |