
中文名称:盐酸帕洛诺司琼
CAS号:135729-62-3
分子式: C19H24N2O.HCl 分子量: 332.87
产品形式: HCL
研发状态: Completed
研发用途: Healthy
研究机构: HK inno.N Corporation
研发日期: March 18 2021
研发阶段: Phase 1
Palonosetron HCl (RS 25259, RS 25259 197) is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting.
中文名称:帕洛诺司琼
CAS号:135729-61-2
分子式: C19H24N2O 分子量: 296.41
产品形式: Free Base
研发状态: Completed
研发用途: Healthy
研究机构: HK inno.N Corporation
研发日期: March 18 2021
研发阶段: Phase 1
Palonosetron (RS25259, RS 25259 197) is a 5-HT3 antagonist with Ki value of 0.17 nM. It is used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV).
中文名称:(S)-1-(3-((6-(6-甲氧基-5-(三氟甲基)吡啶-3-基)-5,6,7,8-四氢吡啶并[4,3-D]嘧啶-4-基)氨基)吡咯烷-1-基)丙-1-酮
CAS号:1354690-24-6
分子式: C21H25F3N6O2 分子量: 450.46
产品形式: Free Base
研发状态: Recruiting
研发用途: APDS Gene Mutation
研究机构: Pharming Technologies B.V.; Laboratory Corporation of America; Axial Biotech Inc; CMIC Co Ltd. Japan
研发日期: August 3 2023
研发阶段: Phase 3
Leniolisib (CDZ 173) is a potent PI3Kδ selective inhibitor with biochemical IC50 values of 0.244, 0.424, 2.23 and 0.011 μM for PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ, respectively.
中文名称: 考拉西坦
CAS号:135463-81-9
分子式: C19H23N3O3 分子量: 341.40
产品形式: free base
研发状态: Completed
研发用途: Major Depressive Disorder; Anxiety
研究机构: BrainCells Inc.
研发日期: Jan-08
研发阶段: Phase 2
Coluracetam (BCI-540, MKC-231) is a nootropic belonging to the racetam family of drugs with cognitive enhancing and neuroprotective effects.
中文名称: 雷尼酸锶
CAS号:135459-87-9
分子式: C12H6N2O8S.2Sr 分子量: 513.49
产品形式: Free base
研发状态: Completed
研发用途: Postmenopausal Osteoporosis; Compliance
研究机构: University of Valencia
研发日期: Sep-09
研发阶段: Phase 4
Strontium Ranelate is a strontium(II) salt of ranelic acid for (-)-desmethoxyverapamil binding to calcium channel with IC50 of 0.5 mM.
中文名称:哌仑他韦
CAS号:1353900-92-1
分子式: C57H65F5N10O8 分子量: 1113.18
产品形式: free base
研发状态: Completed
研发用途: Hepatitis C Virus (HCV)
研究机构: AbbVie
研发日期: October 7 2020
研发阶段: --
Pibrentasvir (ABT-530) is a novel and pan-genotypic hepatitis C virus (HCV) NS5A inhibitor with EC50 ranging from 1.4 pM to 5.0 pM against HCV replicons containing NS5A from genotypes 1 to 6.
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