
中文名称:西地那非
CAS号:139755-83-2
分子式: C22H30N6O4S 分子量: 474.58
产品形式: free base
研发状态: Not yet recruiting
研发用途: Erectile Dysfunction and Neutrophil Lymphocyte Ratio
研究机构: Assiut University
研发日期: August 1 2022
研发阶段: Early Phase 1
Sildenafil (Revatio, UK-92480, Viagra) is a Phosphodiesterase 5 Inhibitor with IC50 of 5.22 nM.
CAS号:1394820-69-9
分子式: C31H29FN4O5 分子量: 556.58
产品形式: free base
研发状态: Not yet recruiting
研发用途: Advanced NSCLC
研究机构: Sunshine Lake Pharma Co. Ltd.
研发日期: November 27 2022
研发阶段: Phase 2
Ningetinib (CT-053, DE-120, CT053PTSA) is a potent, orally bioavailable inhibitor of tyrosine kinase with IC50 of 6.7 nM, 1.9 nM and <1.0 nM for c-Met, VEGFR2 and Axl, respectively. Ningetinib exhibits antitumor activity.
中文名称:坎地沙坦
CAS号:139481-59-7
分子式: C24H20N6O3 分子量: 440.45
产品形式: free base
研发状态: Recruiting
研发用途: Cardiomyopathy Dilated
研究机构: Cristina Avendaño Solá; Puerta de Hierro University Hospital
研发日期: June 2 2022
研发阶段: Phase 3
Candesartan (CV-11974) is an angiotensin II receptor antagonist with IC50 of 0.26 nM.
中文名称:噻托溴铵
CAS号:139404-48-1
分子式: C19H22NO4S2.Br.xH2O 分子量: 490.43
产品形式: quaternary-N bromide salt&hydr
研发状态: Completed
研发用途: Healthy Volunteers
研究机构: Orion Corporation Orion Pharma
研发日期: February 16 2022
研发阶段: Phase 1
Tiotropium Bromide hydrate (BA 679BR) is a monohydrate of tiotropium bromide (Spiriva; Tiova; BA 679BR; tiopropium) that is an anticholinergic and bronchodilator and a muscarinic receptor antagonist.
中文名称:塞利尼索
CAS号:1393477-72-9
分子式: C17H11F6N7O 分子量: 443.31
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研发状态: Withdrawn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
Selinexor (KPT-330, ATG-010) is an orally bioavailable selective CRM1 inhibitor. Phase 2.
CAS号:1393466-87-9
分子式: C25H21F3N6O3S 分子量: 542.53
产品形式: Free Base
研发状态: Terminated
研发用途: Melanoma; Thyroid Cancer; Colorectal Cancer; Non-small Cell Lung Cancer; Cholangiocarcinoma; Histiocytosis; Hairy Cell Leukemia
研究机构: Fore Biotherapeutics
研发日期: Feb-14
研发阶段: Phase 1
PLX8394 is a next-generation, orally available, small-molecule BRAF inhibitor with IC50 values of 3.8 nM, 14 nM and 23 nM for BRAF(V600E), WT BRAF and CRAF respectively. It has potential antineoplastic activity.
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