
中文名称:反式-2-苯基环丙胺盐酸盐
CAS号:1986-47-6
分子式: C9H12ClN 分子量: 169.65
产品形式: Hydrochloride
研发状态: Completed
研发用途: Major Depressive Disorder; Treatment Resistant Depression
研究机构: Centre for Addiction and Mental Health
研发日期: April 15 2021
研发阶段: Not Applicable
Tranylcypromine HCl (2-PCPA, SKF-385, Parnate) is a monoamine oxidase inhibitor, which inhibits CYP2A6 with Ki of 0.08 μM and 0.2 μM in cDNA-expressing microsomes and Human Liver Microsomes, respectively.
中文名称:醋酸巴多昔芬
CAS号:198481-33-3
分子式: C30H34N2O3.C2H4O2 分子量: 530.65
产品形式: Acetate
研发状态: Unknown status
研发用途: Osteoporosis Postmenopausal
研究机构: Huons Co. Ltd.
研发日期: January 11 2018
研发阶段: Phase 1
Bazedoxifene Acetate (WAY-140424,TSE-424 acetate) is a third generation selective estrogen receptor modulator (SERM).
中文名称:盐酸巴多昔芬
CAS号:198480-56-7
分子式: C30H34N2O3.HCl 分子量: 507.06
产品形式: Hydrochloride
研发状态: Unknown status
研发用途: Osteoporosis Postmenopausal
研究机构: Huons Co. Ltd.
研发日期: January 11 2018
研发阶段: Phase 1
Bazedoxifene HCl (WAY-140424, TSE-424) is a novel, non-steroidal, indole-based estrogen receptor modulator (SERM) binding to both ERα and ERβ with IC50 of 23 nM and 89 nM, respectively.
中文名称:盐酸胺碘酮
CAS号:19774-82-4
分子式: C25H29I2NO3.HCl 分子量: 681.77
产品形式: Hydrochloride
研发状态: Not yet recruiting
研发用途: Atrial Fibrillation; Esophageal Carcinoma
研究机构: OHSU Knight Cancer Institute
研发日期: May 1 2024
研发阶段: Phase 2
Amiodarone (NSC 85442,Amiodar,Amiodarone hydrochloride,Nexterone) HCl is a sodium/potassium-ATPase inhibitor and an autophagy activator, used to treat various types of cardiac dysrhythmias.
中文名称:美司那
CAS号:19767-45-4
分子式: C2H5NaO3S2 分子量: 164.18
产品形式: Sodium Salt
研发状态: Completed
研发用途: Obesity; Drug Effect
研究机构: University of Oslo; Oslo University Hospital; University of Oxford
研发日期: November 2 2020
研发阶段: Phase 1
Mesna, a sulfhydryl compound that is used to reduce the incidence of hemorrhagic cystitis associated with certain chemotherapeutic agents.
中文名称:(R)-1-(1-丙烯酰基哌啶-3-基)-4-氨基-3-(4-苯氧基苯基)-1H-咪唑并[4,5-C]吡啶-2(3H)-酮
CAS号:1971920-73-6
分子式: C₂₆H₂₅N₅O₃ 分子量: 455.51
产品形式: Free base
研发状态: Completed
研发用途: Hepatic Function Abnormal
研究机构: Sanofi
研发日期: March 18 2022
研发阶段: Phase 1
Tolebrutinib (SAR442168, PRN2246, BTKi'168, BTKi('168)) is an oral, CNS-penetrant, irreversible inhibitor of Bruton's tyrosine kinase (BTK) with IC50s of 0.4 nM and 0.7 nM in Ramos B cells and in HMC microglia cells, respectively.
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