
中文名称:依托考昔
CAS号:202409-33-4
分子式: C18H15ClN2O2S 分子量: 358.84
产品形式: free base
研发状态: Unknown status
研发用途: Effect of Drug
研究机构: Dow University of Health Sciences
研发日期: January 1 2022
研发阶段: Early Phase 1
Etoricoxib (Arcoxia, MK-663, MK-0663, Tauxib, Algix, Nucoxia) is a new COX-2 selective inhibitor with anti-inflammatory, antipyretic, analgesic, and potential antineoplastic properties.
CAS号:202402-01-5
分子式: C13H16F3NO2 分子量: 275.27
产品形式: free base
研发状态: Completed
研发用途: Alcohol Dependence
研究机构: Laboratorio Farmaceutico Ct S.r.l.; Voisin Consulting Inc.; Latis S.r.l.; Quotient Bioresearch
研发日期: Nov-14
研发阶段: Phase 1 : Phase 2
GET-73(Gamma hydroxybutyric acid analogue,GET 73,GHB analogue), a γ-hydroxybutyrate (GHB) analog, shows a neuroprotective role against ethanol-induced neurotoxicity in primary cultures of rat hippocampal neurons.
中文名称:比拉斯汀
CAS号:202189-78-4
分子式: C28H37N3O3 分子量: 463.61
产品形式: free base
研发状态: Completed
研发用途: Chronic Urticaria
研究机构: Charite University Berlin Germany
研发日期: Jul-14
研发阶段: Phase 3
Bilastine is a new, well-tolerated, nonsedating H1 receptor antihistamine and has a rapid onset and prolonged duration of action.
中文名称:富马酸替诺福韦酯
CAS号:202138-50-9
分子式: C19H30N5O10P.C4H4O4 分子量: 635.51
产品形式: Fumarate
研发状态: Recruiting
研发用途: Chronic Hepatitis b Patients
研究机构: Sohag University
研发日期: April 15 2023
研发阶段: --
Tenofovir Disoproxil Fumarate (Tenofovir DF,GS-1278 Disoproxil Fumarate) belongs to a class of antiretroviral drugs, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination.
中文名称:盐酸阿米洛利
CAS号:2016-88-8
分子式: C6H8ClN7O.HCl 分子量: 266.09
产品形式: Hydrochloride
研发状态: Recruiting
研发用途: Bipolar Disorder
研究机构: Assistance Publique - Hôpitaux de Paris
研发日期: January 11 2023
研发阶段: Phase 4
Amiloride (MK-870 HCl) is a selective T-type calcium channel blocker, an epithelial sodium channel blocker and a selective inhibitor of urokinase plasminogen activator (uPA)(Ki=7 μM).
中文名称:地拉罗司
CAS号:201530-41-8
分子式: C21H15N3O4 分子量: 373.36
产品形式: free base
研发状态: Recruiting
研发用途: Iron Overload
研究机构: University of Pisa; IRCCS Burlo Garofolo; University of Genova
研发日期: September 30 2020
研发阶段: --
Deferasirox (ICL-670, CGP-72670) is an iron chelator, also a cytochrome P450 3A4 inducer, Cytochrome P450 2C8 inhibitor, and Cytochrome P450 1A2 inhibitor. Deferasirox-induced iron depletion promotes BclxL downregulation and cell death.
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