
CAS号:2070015-26-6
分子式: C31H31N5O2S2.HCl 分子量: 606.20
产品形式: hydrochloride
研发状态: Completed
研发用途: Diabetes Mellitus Type 2
研究机构: Sirtris a GSK Company; GlaxoSmithKline
研发日期: June 3 2011
研发阶段: Phase 1
SRT3025 is an orally available small molecule activator of the SIRT1 enzyme.
中文名称:硫酸长春新碱
CAS号:2068-78-2
分子式: C46H58N4O14S 分子量: 923.04
产品形式: free base
研发状态: Recruiting
研发用途: Pediatric Cancer
研究机构: Moi University; Princess Maxima Center for Pediatric Oncology; Amsterdam UMC location VUmc
研发日期: April 20 2023
研发阶段: Phase 4
Vincristine sulfate (NSC-67574, Leurocristine, Oncovin, 22-Oxovincaleukoblastine) is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 μM in a cell-free assay. Vincristine sulfate induces apoptosis.
中文名称:2-醛基-4-甲氧基苯硼酸
CAS号:206873-63-4
分子式: C38H38N4O6 分子量: 646.73
产品形式: free base
研发状态: Completed
研发用途: Epilepsies Partial
研究机构: National Institute of Neurological Disorders and Stroke (NINDS); National Institutes of Health Clinical Center (CC)
研发日期: July 31 2012
研发阶段: --
Tariquidar (XR9576) is a potent and selective noncompetitive inhibitor of P-glycoprotein with Kd of 5.1 nM in CHrB30 cell line, reverses drug resistance in MDR cell Lines. Phase 3.
中文名称:地瑞拉韦
CAS号:206361-99-1
分子式: C27H37N3O7S 分子量: 547.66
产品形式: free base
研发状态: Not yet recruiting
研发用途: HIV Infections
研究机构: PENTA Foundation; AMS-PHPT Research Collaboration; Institut National de la Santé Et de la Recherche Médicale France; Centre Mère et Enfant de la Fondation Chantal Biya; Centre Hospitalier National d''Enfants Albert Royer; University of Zimbabwe Clinical Research Centre (UZCRC); Baylor College of Medicine
研发日期: Jun-24
研发阶段: Phase 1 : Phase 2
Darunavir (TMC114,DRV) is a nonpeptidic HIV protease inhibitor, used to treat HIV infection.
CAS号:2057509-72-3
分子式: C22H28ClN5O2 分子量: 429.94
产品形式: free base
研发状态: Completed
研发用途: Relapsed/Refractory Peripheral T-cell Lymphoma; Relapsed/Refractory Classical Hodgkins Lymphoma
研究机构: AstraZeneca
研发日期: December 15 2021
研发阶段: Phase 2
AZD4573 is a potent inhibitor of CDK9 (IC50 of <0.004 μM) with fast-off binding kinetics (t1/2 = 16 min) and high selectivity versus other kinases, including other CDK family kinases.
CAS号:2055597-12-9
分子式: C22H25ClFN7O2 分子量: 473.93
产品形式: Free base
研发状态: Active not recruiting
研发用途: Advanced or Metastatic Solid Tumors
研究机构: Erasca Inc.
研发日期: May 7 2021
研发阶段: Phase 1 : Phase 2
ASN007(ERAS 007, ERK-IN-3) is a potent and orally active inhibitor of ERK. ERK-IN-3 inhibits ERK1/2 with 2 nM IC50 values. ERK-IN-3 can be used for the research of cancers driven by RAS mutations.
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