
中文名称:4-[[2-(3-氯苯基)-6-(三氟甲基)-4-吡啶基]甲基]-苯乙酸
CAS号:1606974-33-7
分子式: C21H15ClF3NO2 分子量: 405.80
产品形式: Free Base
研发状态: Enrolling by invitation
研发用途: Fragile X Syndrome
研究机构: Tetra Discovery Partners
研发日期: November 1 2022
研发阶段: Phase 3
Zatolmilast (BPN14770) is a selective allosteric inhibitor of phosphodiesterase 4D (PDE4D) with IC50 of 7.8 nM and 7.4 nM for PDE4D7 and PDE4D3, respectively.
中文名称:5-硝酸异山梨酯
CAS号:16051-77-7
分子式: C6H9NO6 分子量: 191.14
产品形式: Free Base
研发状态: Unknown status
研发用途: Recurrent Pregnancy Loss
研究机构: Al-Azhar University
研发日期: May 1 2022
研发阶段: Early Phase 1
Isosorbide mononitrate (Elantan, Monoket, Mononit, Imdur, Corangin) is a Nitrate Vasodilator, dilating the blood vessels so as to reduce the blood pressure.
中文名称:葡萄糖酸锑钠
CAS号:16037-91-5
分子式: C12H35Na3O26Sb2 分子量: 907.88
产品形式: Sodium
研发状态: Recruiting
研发用途: Primary Visceral Leishmaniasis
研究机构: Drugs for Neglected Diseases; Novartis Pharmaceuticals
研发日期: April 3 2024
研发阶段: Phase 2
Sodium stibogluconate (SSG, Stibogluconate trisodium nonahydrate, Lenocta, VQD-001), a pentavalent antimony derivative, is a potent and selective inhibitor of protein tyrosine phosphatase (PTPase). Sodium stibogluconate inhibits 99% of Src homology 2 domain-containing phosphatase 1 (SHP-1) activity at 10 μg/ml and similar degrees of inhibition of SHP-2 and PTP1B requires 100 μg/ml. Sodium stibogluconate is a drug used in treatment of leishmaniasis.
中文名称:4-碘-3-硝基-苯甲酰胺
CAS号:160003-66-7
分子式: C7H5IN2O3 分子量: 292.03
产品形式: free base
研发状态: Completed
研发用途: Advanced Solid Tumors
研究机构: Sanofi
研发日期: Jul-10
研发阶段: Phase 1
Iniparib (BSI-201, NSC-746045, IND-71677) is a PARP1 inhibitor with demonstrated effectiveness in triple-negative breast cancer (TNBC). Phase 3.
中文名称:甲磺酸奈非那韦
CAS号:159989-65-8
分子式: C33H49N3O7S2 分子量: 663.89
产品形式: Mesylate
研发状态: Completed
研发用途: Human Immunodeficiency Virus
研究机构: Pfizer
研发日期: Aug-02
研发阶段: Phase 2
Nelfinavir Mesylate (Viracept, AG1343) is a potent HIV protease inhibitor with Ki of 2 nM.
CAS号:1599440-33-1
分子式: C26H24FN3O6 分子量: 493.48
产品形式: free base
研发状态: Not yet recruiting
研发用途: Non-Small Cell Lung Carcinoma; Advanced Non-Small Cell Squamous Lung Cancer; EGFR Gene Mutation
研究机构: The Netherlands Cancer Institute; Daiichi Sankyo
研发日期: May 1 2024
研发阶段: Phase 2
Dxd(Exatecan derivative for ADC) is a potent DNA topoisomerase I inhibitor, with an IC50 of 0.31 μM.
即日起可免费注册成为会员, 建立企业产品库, 免费上传产品目录, 企业介绍等. 让你的产品直接呈现给客户.
试运营阶段,所有广告业务5折优惠
