CA2786289A1 - Methods and compositions of targeted drug development - Google Patents
Methods and compositions of targeted drug development Download PDFInfo
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- CA2786289A1 CA2786289A1 CA2786289A CA2786289A CA2786289A1 CA 2786289 A1 CA2786289 A1 CA 2786289A1 CA 2786289 A CA2786289 A CA 2786289A CA 2786289 A CA2786289 A CA 2786289A CA 2786289 A1 CA2786289 A1 CA 2786289A1
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Classifications
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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- C07D403/12—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 chain containing hetero atoms as chain links
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- C07D405/02—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 two hetero rings
- C07D405/06—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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B15/00—ICT specially adapted for analysing two-dimensional or three-dimensional molecular structures, e.g. structural or functional relations or structure alignment
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- G—PHYSICS
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| EP2891649B1 (en) * | 2010-02-17 | 2018-04-11 | Cornell University | Prolylhydroxylase inhibitors and methods of use |
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| JP2013526576A (ja) * | 2010-05-18 | 2013-06-24 | アメリカ合衆国 | ヒト12−リポキシゲナーゼ阻害剤 |
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| WO2012012653A1 (en) * | 2010-07-21 | 2012-01-26 | Errico Joseph P | Combination therapy with mdm2 and efgr inhibitors |
| KR20140028078A (ko) | 2011-05-23 | 2014-03-07 | 온코 바이오메디컬 테크놀로지 (수조우) 코., 엘디디. | 씨디씨42 억제제 및 이의 용도 |
| CA2839703A1 (en) | 2011-06-24 | 2012-12-27 | Amgen Inc. | Trpm8 antagonists and their use in treatments |
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| EP2850514A4 (en) * | 2012-05-18 | 2016-03-02 | Univ Georgetown | METHOD AND SYSTEMS FOR FACILITATING AND SEARCHING A DATABASE OF INFORMATION ON MEDICINAL PRODUCTS |
| US20150133450A1 (en) * | 2012-06-20 | 2015-05-14 | Eutropics Pharmaceuticals, Inc. | Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives |
| US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
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| CN105377837B (zh) | 2013-05-14 | 2017-08-04 | 活跃生物技术有限公司 | 用作s100‑抑制剂的n‑(杂芳基)磺酰胺衍生物 |
| US10732182B2 (en) | 2013-08-01 | 2020-08-04 | Eutropics Pharmaceuticals, Inc. | Method for predicting cancer sensitivity |
| KR20160128288A (ko) * | 2013-10-07 | 2016-11-07 | 리서치 파운데이션 오브 더 시티 유니버시티 오브 뉴욕 | 수계 약리작용단을 이용하는 방법 |
| US10640803B2 (en) | 2013-10-30 | 2020-05-05 | Eutropics Pharmaceuticals, Inc. | Methods for determining chemosensitivity and chemotoxicity |
| CN104016908B (zh) * | 2014-04-03 | 2016-04-20 | 定陶县友帮化工有限公司 | 一种2-氨基-3,5-二氯吡啶的合成方法 |
| CN104402831B (zh) * | 2014-10-24 | 2016-08-17 | 郑州大学 | 含酰脲结构单元的-5-氰基嘧啶衍生物及其制备方法和用途 |
| CN104744439A (zh) * | 2015-02-10 | 2015-07-01 | 南开大学 | 8-羟基喹啉类ntr1小分子拮抗剂及应用 |
| HUP1500098A2 (hu) * | 2015-03-09 | 2016-09-28 | Avidin Kft | 8-hidroxikinolin származékok új enantiomerjei és szintézisük |
| CA3001817A1 (en) * | 2015-10-12 | 2017-04-20 | Health Research, Inc. | Methods for inducing apoptosis in cancer cells |
| EP3388419A1 (en) * | 2017-04-12 | 2018-10-17 | Leadiant Biosciences SA | Gli1 inhibitors and uses thereof |
| WO2019043635A1 (en) | 2017-09-01 | 2019-03-07 | Richter Gedeon Nyrt. | COMPOUNDS INHIBITING THE ACTIVITY OF D-AMINO ACID OXIDASE |
| JP7636322B2 (ja) * | 2018-11-15 | 2025-02-26 | アンスティテュ・ギュスターヴ・ルシー | 癌を処置するためのマドラシン誘導体化合物、組成物およびこれらの使用 |
| TW202218665A (zh) | 2020-09-21 | 2022-05-16 | 德國阿爾伯特路德維希弗萊堡大學 | 用於治療或預防造血細胞移植後血液科贅瘤(neoplasm)復發之mdm2抑制劑 |
| CN112250637A (zh) * | 2020-10-30 | 2021-01-22 | 中山大学 | 虚拟筛选的化合物在制备抗肿瘤药物中的应用及其药物 |
| CN114195691B (zh) * | 2021-12-16 | 2023-10-20 | 贵州大学 | 一种含酰胺的阿魏酸衍生物及其制备方法和应用 |
| WO2024073624A2 (en) * | 2022-09-28 | 2024-04-04 | The Research Foundation For The State University Of New York | Antiproliferative betti bases and prodrugs thereof |
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| CN120463779B (zh) * | 2025-07-10 | 2025-09-19 | 南京农业大学三亚研究院 | 真菌效应子药靶Nep1及基于该药靶的高通量药物分子筛选和应用 |
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| BRPI0611863B1 (pt) * | 2005-06-22 | 2021-11-23 | Plexxikon, Inc | Composto, bem como composição e kit compreendendo o mesmo, composto intermediário na preparação do mesmo, método para tratamento e uso do mesmo |
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| BRPI0709749A2 (pt) | 2006-04-05 | 2011-07-26 | Novartis Ag | combinaÇÕes de agentes terapÊuticos para tratamento de cÂncer |
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| CN102574805A (zh) | 2009-08-20 | 2012-07-11 | 维福(国际)股份公司 | 新型喹啉铁调素拮抗剂 |
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| CA2786277A1 (en) | 2011-07-14 |
| US20110301193A1 (en) | 2011-12-08 |
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| US9073858B2 (en) | 2015-07-07 |
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| KR20130027080A (ko) | 2013-03-14 |
| WO2011085129A3 (en) | 2011-09-01 |
| US20140179681A1 (en) | 2014-06-26 |
| SG182343A1 (en) | 2012-08-30 |
| WO2011085126A2 (en) | 2011-07-14 |
| US8618302B2 (en) | 2013-12-31 |
| EP2521551A2 (en) | 2012-11-14 |
| AU2011204368A1 (en) | 2012-07-19 |
| US20140163069A1 (en) | 2014-06-12 |
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