• TargetMol
    您的购物车当前为空
筛选
已筛选:全部清除
TargetMol | Tags 通过 靶点 筛选
  • Cannabinoid Receptor
    (2)
  • GABA Receptor
    (1)
  • Topoisomerase
    (1)
  • Others
    (3)
TargetMol | Tags 通过 货期 筛选
  • 现货
    (2)
  • 35日内发货
    (2)
抑制剂&激动剂
细分筛选
搜索结果
TargetMol产品目录中 "mg (0:0/10:0/0:0)"的结果
筛选
搜索结果
TargetMol产品目录中 "

mg (0:0/10:0/0:0)

"的结果
  • 抑制剂&激动剂
    4
    抑制剂&激动剂
  • COR659
    T36520544450-68-2
    COR659 是一种有效的 GABAB 的阳性变构调节剂。COR659具有缓解大鼠对酒精和巧克力成瘾的作用。
    • ¥ 343
    现货
    规格
    数量
    TargetMol | Inhibitor Sale
  • Glyceryl 2-Caprate
    2-癸酸甘油酯, 2-Monocaprin, 2-Decanoyloxy-Propan-1,3-Diol, 2-Decanoyl Glycerol
    T319523376-48-5
    Glyceryl 2-Caprate (2-Monocaprin)是一种甘油酯,可用于生物化学实验和药物合成研究。
    • ¥ 1300
    现货
    规格
    数量
  • O-7460
    T357861572051-31-0
    In humans, two forms of diacylglycerol lipase, DAGLα and DAGLβ, generate the endocannabinoid 2-arachidonoyl glycerol by attacking DAG at the sn-1 position. O-7460 is a selective inhibitor of 2-AG biosynthesis via DAGLα (IC50 = 690 nM). It demonstrates much weaker inhibition towards human monoacylglycerol lipase and rat brain fatty acid amide hydrolase (IC50s > 10 μM) and does not bind to CB1 or CB2 cannabinoid receptors (Kis > 10 μM). At 0-12 mg/kg, i.p. in mice, O-7460 was reported to dose-dependently inhibit high-fat diet intake and reduce body weight.
    • ¥ 1980
    35日内发货
    规格
    数量
  • CAY10744
    T361952375613-31-1
    CAY10744 is a topoisomerase II-α poison.1 It inhibits topoisomerase II-α by 78.9% when used at a concentration of 20 μM. CAY10744 is selective for topoisomerase II-α over topoisomerase I providing 100 and 0% inhibition, respectively, at 100 μM. It inhibits proliferation of HCT15 colon, T47D breast, DU145 prostate, and HeLa cervical cancer cells (IC50s = 0.014, 0.00267, 0.072, and 2.46 μM, respectively). CAY10744 induces apoptosis in T47D cells when used at concentrations of 10 and 30 μM. CAY10744 (12 mg/kg per day) reduces tumor growth in an MDA-MB-231 orthotopic mouse model of breast cancer. |1. Kadayat, T.M., Park, S., Shrestha, A., et al. Discovery and biological evaluations of halogenated 2,4-diphenyl indeno[1,2-b]pyridinol derivatives as potent topoisomerase IIa-targeted chemotherapeutic agents for breast cancer. J. Med. Chem. 62, 8194-8234 (2019).
    • ¥ 1430
    35日内发货
    规格
    数量