
中文名称:奥美沙坦酯
CAS号:144689-63-4
分子式: C29H30N6O6 分子量: 558.59
产品形式: free base
研发状态: Completed
研发用途: Healthy
研究机构: Daiichi Sankyo
研发日期: Nov-04
研发阶段: Phase 4
Olmesartan Medoxomil (CS-866,RNH-6270) is a selective angiotensin II type 1 (AT(1)) receptor antagonist, used in the treatment of high blood pressure.
中文名称:奥美沙坦
CAS号:144689-24-7
分子式: C24H26N6O3 分子量: 446.50
产品形式: free base
研发状态: Completed
研发用途: Healthy Adult Volunteers
研究机构: Autotelicbio
研发日期: June 19 2021
研发阶段: Phase 1
Olmesartan (RNH-6270) is an an angiotensin 2 receptor antagonist with antihypertensive activity.
中文名称:匹杉群马来酸盐
CAS号:144675-97-8
分子式: C17H19N5O2.2C4H4O4 分子量: 557.51
产品形式: dimaleate
研发状态: Completed
研发用途: Acute Myelogenous Leukemia
研究机构: CTI BioPharma
研发日期: Mar-05
研发阶段: Phase 1 : Phase 2
Pixantrone (BBR-2778) is a novel aza-anthracenedione compound with antitumor activity. It is a weak topoisomerase II inhibitor and forms stable DNA adducts through alkylation with specificity for DNA hypermethylated sites.
中文名称:伊那尼布
CAS号:1446502-11-9
分子式: C19H17F6N7O 分子量: 473.38
产品形式: free base
研发状态: Recruiting
研发用途: IDH Mutation; IDH1 Mutation; IDH2 Gene Mutation; Blood Cancer; Myeloproliferative Neoplasm
研究机构: University of Chicago
研发日期: October 29 2021
研发阶段: Phase 1
Enasidenib (AG-221) is a first-in-class, oral, potent, reversible, selective inhibitor of the IDH2 mutant enzyme.
中文名称:伏塞洛托
CAS号:1446321-46-5
分子式: C19H19N3O3 分子量: 337.37
产品形式: free base
研发状态: Recruiting
研发用途: Sickle Cell Disease
研究机构: Inova Health Care Services; Pfizer
研发日期: October 23 2023
研发阶段: Phase 2
Voxelotor (GBT440, GTx011) is a novel small molecule hemoglobin modifier which increases hemoglobin oxygen affinity.
CAS号:1446261-44-4
分子式: C16H15FN4O 分子量: 298.31
产品形式: Free Base
研发状态: Recruiting
研发用途: Neoadjuvant Therapy
研究机构: Hongqian Guo; First Affiliated Hospital of Zhejiang University; The First Affiliated Hospital of Soochow University; Nanjing First Hospital Nanjing Medical University; The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
研发日期: February 22 2022
研发阶段: Phase 2
Pamiparib (BGB-290) is a potent and selective inhibitor of PARP1 and PARP2 with IC50 values of 0.83 and 0.11 nM, respectively in biochemical assays. It shows high selectivity over other PARP enzymes.
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