
中文名称:伊达萨努特林(RG-7388)
CAS号:1229705-06-9
分子式: C31H29Cl2F2N3O4 分子量: 616.48
产品形式: free base
研发状态: Withdrawn
研发用途: Rhabdoid Tumor; Atypical Teratoid/Rhabdoid Tumor; Atypical Teratoid/Rhabdoid Tumor of CNS; CNS Tumor
研究机构: St. Jude Children''s Research Hospital
研发日期: Mar-24
研发阶段: Phase 1
Idasanutlin (RG-7388) is a potent and selective p53-MDM2 inhibitor with IC50 of 6 nM showing improved in vitro binding as well as cellular potency/selectivity.
中文名称:盐酸多塞平
CAS号:1229-29-4
分子式: C19H21NO.HCl 分子量: 315.84
产品形式: hydrochloride
研发状态: Completed
研发用途: Head and Neck Cancer; Mucositis; Oral Complications of Radiation Therapy; Pain
研究机构: Alliance for Clinical Trials in Oncology; National Cancer Institute (NCI)
研发日期: Dec-10
研发阶段: Phase 3
Doxepin is a tricyclic antidepressant formulated as a mixture of E-(trans) and Z-(cis) stereoisomers. It inhibits CYP2D6 activity in vivo.
中文名称:盐酸巴多昔芬
CAS号:1229236-86-5
分子式: C23H25ClFN7O 分子量: 469.94
产品形式: free base
研发状态: Completed
研发用途: Myeloproliferative Neoplasms of; Polycythemia Vera; Essential Thrombocythemia; Myelofibrosis
研究机构: Eli Lilly and Company
研发日期: June 11 2012
研发阶段: Phase 1
Gandotinib (LY2784544) is a potent JAK2 inhibitor with IC50 of 3 nM, effective in JAK2V617F, 8- and 20-fold selective versus JAK1 and JAK3. Phase 2.
中文名称:伊多塞班对甲苯磺酸盐一水合物
CAS号:1229194-11-9
分子式: C24H30ClN7O4S.C7H8O3S.H2O 分子量: 738.27
产品形式: Tosylate hydrate
研发状态: Recruiting
研发用途: Drug-drug Interaction
研究机构: Radboud University Medical Center; Astellas Pharma Inc
研发日期: July 1 2024
研发阶段: --
Edoxaban (DU-176b) is a selective factor Xa inhibitor with Ki of 0.561 nM, >10 000-fold selectivity over thrombin and FIXa, and is also an orally bioavailable anticoagulant drug.
中文名称:盐酸齐拉西酮
CAS号:122883-93-6
分子式: C21H21ClN4OS.HCl 分子量: 449.40
产品形式: Hydrochloride
研发状态: Completed
研发用途: Schizophrenia; Bipolar Disorder
研究机构: Medco Health Solutions Inc.; SureGene LLC
研发日期: Dec-10
研发阶段: --
Ziprasidone HCl (CP-88059) is a novel and potent dopamine and serotonin (5-HT) receptor antagonist, used in the treatment of schizophrenia and bipolar disorder.
中文名称:7-[6-(2-羟基丙-2-基)吡啶-3-基]-1-(反式-4-甲氧基环己基)-3,4-二氢吡嗪并[2,3-B]吡嗪-2(1H)-酮
CAS号:1228013-30-6
分子式: C21H27N5O3 分子量: 397.47
产品形式: free base
研发状态: Terminated
研发用途: Lymphoma Large B-Cell Diffuse
研究机构: Celgene
研发日期: December 18 2013
研发阶段: Phase 1
Onatasertib (CC 223) is a potent, selective, and orally bioavailable mTOR inhibitor with IC50 of 16 nM, >200-fold selectivity over the related PI3K-α. Phase 1/2.
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