
中文名称:白消安
CAS号:55-98-1
分子式: C6H14O6S2 分子量: 246.30
产品形式: free base
研发状态: Not yet recruiting
研发用途: Acute Leukemia; Mielodysplasic Syndrome; Myeloproliferative Neoplasm
研究机构: Institut Paoli-Calmettes
研发日期: Nov-20
研发阶段: Phase 2
Busulfan (NSC-750) is a cell cycle non-specific alkylating antineoplastic agent. Busulfan induces apoptosis.
中文名称:17,21-二丙酸倍他米松酯
CAS号:5593-20-4
分子式: C28H37FO7 分子量: 504.59
产品形式: Free Base
研发状态: Completed
研发用途: Healthy
研究机构: LEO Pharma
研发日期: March 20 2018
研发阶段: Phase 1
Betamethasone Dipropionate (SCH 11460) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive abilities.
中文名称:N’-(1H-苯并咪唑-2-甲基)-N’-((S)-5,6,7,8-四氢喹啉-8-基)丁烷-1,4-二胺
CAS号:558447-26-0
分子式: C21H27N5 分子量: 349.47
产品形式: free base
研发状态: Active not recruiting
研发用途: Neutropenia
研究机构: X4 Pharmaceuticals
研发日期: October 16 2020
研发阶段: Phase 1 : Phase 2
Mavorixafor (AMD-070) is a potent, selective CXCR4 antagonist, with an IC50 value of 13 nM against CXCR4 125I-SDF binding.
中文名称:氢溴酸常山酮
CAS号:55837-20-2
分子式: C16H17BrClN3O3 分子量: 414.68
产品形式: free base
研发状态: Not yet recruiting
研发用途: Cirrhosis Liver
研究机构: University of Texas Southwestern Medical Center; National Cancer Institute (NCI)
研发日期: Jul-24
研发阶段: Phase 2
Halofuginone (RU-19110) is the competitively inhibitor of prolyl-tRNA synthetase with Ki of 18.3 nM.It could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in mammal.
中文名称: 盐酸倍他司汀
CAS号:5579-84-0
分子式: C8H12N2.2HCl 分子量: 209.12
产品形式: 2HCl
研发状态: Completed
研发用途: Healthy
研究机构: OBEcure Ltd.
研发日期: Feb-09
研发阶段: Phase 1
Betahistine (PT-9) is a histamine H3 receptor inhibitor with IC50 of 1.9 μM.
中文名称: 舒尼替尼
CAS号:557795-19-4
分子式: C22H27FN4O2 分子量: 398.47
产品形式: free base
研发状态: Not yet recruiting
研发用途: Carcinoma Renal Cell
研究机构: State University of New York at Buffalo
研发日期: June 1 2024
研发阶段: Phase 1 : Phase 2
Sunitinib (SU11248) is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM, and also inhibits c-Kit. Sunitinib is also a dose-dependent inhibitor of the autophosphorylation activity of IRE1α. Sunitinib induces autophagy and apoptosis.
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