购物车
  • 全部删除
  • 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
  • Antibacterial
    (1)
  • Antifungal
    (1)
  • Apoptosis
    (1)
  • CDK
    (1)
TargetMol | Tags 通过 货期 筛选
  • 现货
    (4)
  • 5日内发货
    (1)
  • 35日内发货
    (1)
  • 6-8周
    (1)
筛选
搜索结果
TargetMol产品目录中 "

cp 20

"的结果
  • 抑制剂&激动剂
    7
    TargetMol | Inhibitors_Agonists
  • 同位素
    1
    TargetMol | Isotope_Products
  • 疾病造模
    1
    TargetMol | Disease_Modeling_Products
  • Deferiprone
    去铁酮, Deferidone, 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
    In stock
    规格
    数量
  • CP-20961
    T1500335607-20-6
    CP-20961 is a synthetic non-immunogenic adjuvant. It induces arthritis.
    • 待估
    35日内发货
    规格
    数量
  • Tofacitinib Citrate
    柠檬酸托法替尼, 枸橼酸托法替尼, Tofacitinib (CP-690550) Citrate, Tasocitinib citrate, 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
    In stock
    规格
    数量
  • Prostaglandin G/H synthase 1 inhibitor
    CP74006, 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。
    • ¥ 158
    In stock
    规格
    数量
    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
    规格
    数量
  • Erlotinib-13C6
    Erlotinib-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
    待询
    规格
    数量
  • CDK5 inhibitor 20-223
    CP668863, CP 668863
    T36742865317-30-2
    CDK5 inhibitor 20-223(CP668863)是一种高效的CDK2 CDK5抑制剂,IC50值分别为6.0 nm和8.8 nM,具有抗结直肠癌(CRC)的潜力,在多种CRC细胞系中抑制细胞迁移和诱导细胞周期阻滞。
    • ¥ 987
    In stock
    规格
    数量