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TargetMol产品目录中 "

cp 20

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  • 抑制剂&激动剂
    5
    TargetMol | Inhibitors_Agonists
  • 同位素
    1
    TargetMol | Isotope_Products
DeferiproneDeferidone,去铁酮,CP20
T156530652-11-0
Deferiprone (Deferidone) 是口服活性铁螯合剂,可研究地中海贫血中的输血性铁过载。
  • ¥ 195
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TargetMol | Citations 客户已引用
Tofacitinib CitrateCP-690550 citrate,枸橼酸托法替尼,柠檬酸托法替尼,Tasocitinib citrate,Tofacitinib (CP-690550) Citrate
T2398540737-29-9
Tofacitinib Citrate (CP-690550 citrate) 是 JAK1 2 3抑制剂,IC50分别为112,20 和 1 nM。它具有抗菌,抗真菌和抗病毒活性。
  • ¥ 297
现货
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Prostaglandin G/H synthase 1 inhibitorCP74006,CP 74006,2-Amino-N-(4-chlorophenyl)benzamide
T270664943-86-6
Prostaglandin G H synthase 1 inhibitor (CP 74006) 是一种选择性D5D 抑制剂,IC(50)值为20nM。
  • ¥ 127
现货
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TargetMol | Inhibitor Sale
CP-96486
T10873139401-45-9In house
CP-96486 is a potent and orally active antagonist of leukotriene D4 (LTD4) platelet activating factor (PAF) receptor (Kis: 20 and 24 nM).
  • ¥ 10600
8-10周
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Erlotinib-13C6Erlotinib-13C6
T359151211107-68-4
Erlotinib-13C6 (CP-358774-13C6) is a 13C-labeled Erlotinib. Erlotinib is a directly acting EGFR tyrosine kinase inhibitor, with an IC50 of 2 nM for human EGFR[1]. Erlotinib reduces EGFR autophosphorylation in intact tumor cells with an IC50 of 20 nM. Erlotinib is used for the treatment of non-small cell lung cancer[1].Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process[2]. [1]. Moyer JD, et al. Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor receptor tyrosine kinase. Cancer Res. 1997, 57(21), 4838-4848.[2]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.
  • ¥ 13917
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