
中文名称:(2R)-2,4-二甲基-1-哌嗪羧酸 4-[(3-氯-2-氟苯基)氨基]-7-甲氧基-6-喹唑啉基酯
CAS号:1626387-80-1
分子式: C22H23ClFN5O3 分子量: 459.90
产品形式: free base
研发状态: Completed
研发用途: EGFR Mutation Positive Advanced Non Small Cell Lung Cancer
研究机构: AstraZeneca
研发日期: November 5 2014
研发阶段: Phase 1
Zorifertinib (AZD3759) is a potent, oral active, CNS-penetrant EGFR inhibitor with IC50 of 0.3 nM, 0.2 nM, and 0.2 nM for EGFR (WT), EGFR (L858R), and EGFR (exon 19Del), respectively. Phase 1.
中文名称:西罗莫司脂化物
CAS号:162635-04-3
分子式: C56H87NO16 分子量: 1030.29
产品形式: free base
研发状态: Recruiting
研发用途: High Grade Glioma; Glioma; Glioma Malignant; Glioblastoma
研究机构: Nader Sanai; Barrow Neurological Institute; Ivy Brain Tumor Center; St. Joseph''s Hospital and Medical Center Phoenix
研发日期: May 15 2023
研发阶段: Early Phase 1
Temsirolimus (CCI-779, NSC 683864) is a specific mTOR inhibitor with IC50 of 1.76 μM in a cell-free assay. Temsirolimus induces autophagy and apoptosis.
中文名称:罗氟司特
CAS号:162401-32-3
分子式: C17H14Cl2F2N2O3 分子量: 403.21
产品形式: free base
研发状态: Completed
研发用途: Psoriasis
研究机构: Cairo University
研发日期: January 9 2023
研发阶段: Phase 2 : Phase 3
Roflumilast (APTA 2217, B9302-107, BY 217, BYK 20869) is a selective inhibitor of PDE4 with IC50 of 0.2-4.3 nM in a cell-free assay.
中文名称:盐酸芬戈莫德
CAS号:162359-56-0
分子式: C19H33NO2.HCl 分子量: 343.90
产品形式: Hydrochloride
研发状态: Completed
研发用途: Multiple Sclerosis
研究机构: Novartis Pharmaceuticals; Novartis
研发日期: May 18 2020
研发阶段: --
Fingolimod (FTY720, Fingolimod Hydrochloride) HCl is a S1P antagonist with IC50 of 0.033 nM in K562, and NK cells.
中文名称: 芬戈莫德
CAS号:162359-55-9
分子式: C19H33NO2 分子量: 307.47
产品形式: Free Base
研发状态: Completed
研发用途: Multiple Sclerosis
研究机构: Novartis Pharmaceuticals; Novartis
研发日期: May 18 2020
研发阶段: --
Fingolimod (FTY-720A, FTY-720) is a sphingosine 1-phosphate receptor modulator used for the treatment of relapsing-remitting multiple sclerosis.
CAS号:1623416-31-8
分子式: C21H17N3O2 分子量: 343.38
产品形式: Free Base
研发状态: Terminated
研发用途: Lymphoma
研究机构: Agios Pharmaceuticals Inc.
研发日期: May 24 2019
研发阶段: Phase 1
AG-636 is an orally available inhibitor of dihydroorotate dehydrogenase (DHODH) with potential antineoplastic activity.
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