
中文名称:乌布吉泮
CAS号:1374248-77-7
分子式: C29H26F3N5O3 分子量: 549.54
产品形式: free base
研发状态: Completed
研发用途: Healthy Volunteers
研究机构: AbbVie
研发日期: July 11 2023
研发阶段: Phase 1
Ubrogepant (MK-1602) is an antagonist of human calcitonin gene-related peptide receptor (CGRP). It potently blocks human α–CGRP–stimulated cAMP responses with an IC50 of 0.081 nM in human CGRP receptor-expressing HEK293 cells.
中文名称:双醋瑞因; 二乙酰大黄酸; 二乙酰二氢蒽羧酸
CAS号:13739-02-1
分子式: C19H12O8 分子量: 368.29
产品形式: free base
研发状态: Completed
研发用途: Epidermolysis Bullosa (EB); Epidermolysis Bullosa Simplex; Dystrophic Epidermolysis Bullosa; Junctional Epidermolysis Bullosa
研究机构: Castle Creek Pharmaceuticals LLC
研发日期: May 18 2018
研发阶段: Phase 1
Diacerein is an inhibitor of pro-inflammatory cytokine Interleukin-1B (IL-1B) production, prescribed for osteoarthritis and chronic inflammatory arthritis.
中文名称:N-[(3R,4S)-3,4-二氢-3-[[(甲基氨基)羰基]氧基]-6-[4-(3-氧杂环丁基)-1-哌嗪基]-2H-1-苯并吡喃-4-基]-4-氟-苯甲酰胺
CAS号:1373215-15-6
分子式: C25H29FN4O5 分子量: 484.52
产品形式: free base
研发状态: Completed
研发用途: Healthy Volunteers
研究机构: Eli Lilly and Company
研发日期: Feb-12
研发阶段: Phase 1
LY 3000328 (Z-FL-COCHO, Compound 5) is a potent and selective Cathepsin S (Cat S) inhibitor with IC50s of 7.7 and 1.67 nM for human Cat S and mouse Cat S, respectively.
中文名称:培美曲塞二钠盐
CAS号:137281-23-3
分子式: C20H21N5O6 分子量: 427.41
产品形式: Free Base
研发状态: Recruiting
研发用途: Non Small Cell Lung Cancer Metastatic; ALK Gene Mutation
研究机构: Centro di Riferimento Oncologico - Aviano
研发日期: March 15 2024
研发阶段: Phase 2
Pemetrexed (LY231514, Alimta) is a novel antifolate and antimetabolite for thymidylate synthase (TS), dihydrofolate reductase (DHFR) and glycinamide ribonucleotide formyltransferase (GARFT) with Ki of 1.3 nM, 7.2 nM and 65 nM in cell-free assays, respectively. Pemetrexed induces autophagy and apoptosis.
中文名称:2-甲基-1-[[2-甲基-3-(三氟甲基)苯基]甲基]-6-(4-吗啉基)-1H-苯并咪唑-4-羧酸
CAS号:1372540-25-4
分子式: C22H22F3N3O3 分子量: 433.42
产品形式: free base
研发状态: Active not recruiting
研发用途: Melanoma and Other Malignant Neoplasms of Skin; Metastatic Melanoma
研究机构: M.D. Anderson Cancer Center; National Cancer Institute (NCI); National Institutes of Health (NIH); Merck Sharp & Dohme LLC; GlaxoSmithKline
研发日期: July 17 2017
研发阶段: Phase 1 : Phase 2
GSK2636771 is a potent, orally bioavailable and selective inhibitor of PI3Kβ with >900-fold selectivity over PI3Kα/PI3Kγ and >10-fold over PI3Kδ. Sensitive to PTEN null cell lines.
中文名称: 伏立康唑
CAS号:137234-62-9
分子式: C16H14F3N5O 分子量: 349.31
产品形式: free base
研发状态: Terminated
研发用途: Haematological Malignancies
研究机构: AstraZeneca
研发日期: June 11 2021
研发阶段: Phase 1 : Phase 2
Voriconazole (Vfend,UK-109496) is a new triazole derivative similar to fluconazole and itraconazole that acts by inhibiting fungal cytochrome P-450-dependent, 14-alpha-sterol demethylase-mediated synthesis of ergosterol.
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