
CAS号:2414572-47-5
分子式: C29H29ClN6O4 分子量: 561.03
产品形式: Free Base
研发状态: Terminated
研发用途: Solid Tumor
研究机构: Black Diamond Therapeutics Inc.
研发日期: December 19 2019
研发阶段: Phase 1 : Phase 2
BDTX-189 is a potent and selective inhibitor of allosteric EGFR and HER2 oncogenic mutations with Kd of 0.2 nM, 0.76 nM, 13 nM and 1.2 nM for EGFR, HER2, BLK and RIPK2, reapectively. BDTX-189 exhibits anticancer activity.
中文名称:苯扎米,2-(6-氮杂螺[2.5]辛-6-基)-N-[2-(4,4-二氟-1-哌啶)-6-甲基-4-嘧啶酰]-4-[[(2-羟基)磺酰]氨基]-
CAS号:2410796-79-9
分子式: C26H34F2N6O4S 分子量: 564.65
产品形式: Free base
研发状态: Recruiting
研发用途: High Grade Serous Adenocarcinoma of Ovary; Fallopian Tube Cancer; Primary Peritoneal Carcinoma; Chromosomal Instability
研究机构: Volastra Therapeutics Inc.
研发日期: April 4 2024
研发阶段: Phase 1
AMG 650 (Sovilnesib) is an oral, first in class, selective kinesin-like protein KIF18A inhibitor, can be used for the research of cancer.
CAS号:2401892-75-7
分子式: C31H31ClN4O5 分子量: 575.06
产品形式: free base
研发状态: Completed
研发用途: Healthy
研究机构: Pfizer
研发日期: February 22 2023
研发阶段: Phase 1
Lotiglipron (PF-07081532) is an orally active GLP-1R agonist. It reduces glucose and body weight, and has the potential to be used in Type 2 diabetes mellitus (T2DM) research.
中文名称:盐酸阿替卡因
CAS号:23964-57-0
分子式: C13H20N2O3S.HCl 分子量: 320.84
产品形式: Hydrochloride
研发状态: Completed
研发用途: Healthy
研究机构: American Genomics LLC
研发日期: February 24 2021
研发阶段: Phase 1
Articaine (Ultracaine) is a dental local anesthetic which contains an additional ester group that is metabolized by estearases in blood and tissue.
中文名称:托舍多特
CAS号:238750-77-1
分子式: C21H30N2O6 分子量: 406.47
产品形式: Free base
研发状态: Unknown status
研发用途: Acute Myeloid Leukemia
研究机构: Chroma Therapeutics
研发日期: Jun-10
研发阶段: Phase 2
Tosedostat (CHR2797) is an aminopeptidase inhibitor for LAP, PuSA and Aminopeptidase N with IC50 of 100 nM, 150 nM and 220 nM, respectively, and does not effectively inhibit either PILSAP, MetAP-2, LTA4 hydrolase, or MetAP-2. Phase 2.
中文名称:盐酸氨溴索
CAS号:23828-92-4
分子式: C13H18Br2N2O.HCl 分子量: 414.56
产品形式: Hydrochloride
研发状态: Not yet recruiting
研发用途: Lewy Body Disease
研究机构: Lawson Health Research Institute
研发日期: Jan-25
研发阶段: Phase 1 : Phase 2
AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 μM. Phase 3.
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