“abt”的搜索结果

19 个项目

每页

设置升序顺序
  1. Zotarolimus

    Catalog No. A11950
    Quick View
    mTOR 抑制剂
    Zotarolimus是一种免疫抑制剂,可以抑制FKBP-12结合的IC50为2.8nM。。它是雷帕霉素的半合成衍生物。它设计用于以磷酸胆碱为载体的支架。 了解更多
  2. Veliparib dihydrochloride

    Catalog No. A21356
    Quick View
    PARP inhibitor
    Veliparib dihydrochloride is a potent PARP inhibitor, inhibiting PARP1 and PARP2 with Kis of 5.2 and 2.9 nM, respectively. 了解更多
  3. ABT333

    Catalog No. A13878
    Quick View
    NS5B 抑制剂
    ABT333是NS5B非核苷聚合酶抑制剂。 了解更多
  4. Glecaprevir

    Catalog No. A16948
    Quick View
    HCV NS3/4A protease 抑制剂
    Glecaprevir,也称为ABT-493和A-1282576,是一种新型的HCV NS3/4A蛋白酶抑制剂,IC50值在3.5至11.3 nM之间。 了解更多
  5. Choline Fenofibrate

    Catalog No. A15044
    Quick View
    CYP2C19/CYP2B6 抑制剂
    Choline Fenofibrate (ABT-335)是非诺贝特酸的胆碱盐,与瑞舒伐他汀联合用于治疗血脂异常。 了解更多
  6. Ilorasertib

    Catalog No. A20982
    Quick View
    ATP-competitive multitargeted kinase inhibitor
    Ilorasertib (ABT-348) is a potent and ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A with IC50s of 1 nM, 7 nM, 120 nM, respectively. 了解更多
  7. Lopinavir (ABT-378)

    Catalog No. A10537
    Quick View
    HIV Protease 抑制剂
    Lopinavir (ABT-378)是HIV蛋白酶的抑制剂。 了解更多
  8. Atreleuton

    Catalog No. A18623
    Quick View
    5-Lipoxygenase (5-LO) inhibitor
    Atreleuton (ABT-761) is a selective, reversible, and orally bioavailable 5-Lipoxygenase (5-LO) inhibitor. Atreleuton (ABT-761) exhibits potent and selective inhibition of leukotriene formation. 了解更多
  9. ABT

    Catalog No. A13361
    Quick View
    Cytochrome P450 抑制剂
    ABT (1-Aminobenzotriazole)是(CYP)细胞色素P-450和氯过氧化物酶的自杀底物。 了解更多
  10. ABT-046

    Catalog No. A14984
    Quick View
    DGAT-1 抑制剂
    ABT-046是一种有效的,选择性的,可口服生物利用的二酰基甘油酰基转移酶1(DGAT-1)抑制剂(IC50 = 8 nM)。 了解更多
  11. ABT-737

    Catalog No. A10255
    Quick View
    Bcl-2 抑制剂
    ABT-737是一种类BH3抑制剂,能同时抑制Bcl-xL,Bcl-2和Bcl-w,EC50分别为78.7 nM,30.3 nM和197.8 nM;但对Mcl-1,Bcl-B及Bfl-1没有抑制作用。 了解更多
  12. ABT-263 (Navitoclax)

    Catalog No. A10022
    Quick View
    Bcl-2 抑制剂
    ABT-263 (Navitoclax)是一种有效的Bcl-2家族抑制剂 (Bcl-2,Bcl-xL和Bcl-w的Ki <1 nmol/L)。ABT-263对Bcl- xL,Bcl-2和Bcl-w,( Ki≤1nmol/ L) 维持高亲和力,但与Mcl-1和A1的结合更弱。 了解更多
  13. ABT-888 (Veliparib)

    Catalog No. A10026
    Quick View
    PARP 抑制剂
    ABT-888 (Veliparib)是一种潜在的抗癌药物,可作为PARP抑制剂。 了解更多
  14. ABT-751 (E-7010)

    Catalog No. A10024
    Quick View
    Microtubule Associated 抑制剂
    ABT-751 (E-7010)是一种抗有丝分裂剂,可抑制微管聚合,并在秋水仙碱位点与β-微管蛋白结合。在G2M期阻断细胞周期并诱导凋亡。 了解更多
  15. ABT-199 (Venetoclax)

    Catalog No. A12500
    Quick View
    Bcl-2 抑制剂
    ABT-199 (Venetoclax) 是一种所谓的BH3类似药物,旨在阻断Bcl 2蛋白的功能。 了解更多
  16. Upadacitinib (ABT-494)

    Catalog No. A18316
    Quick View
    JAK-1 抑制剂
    Upadacitinib (ABT-494) is a potent and selective Janus kinase (JAK) 1 inhibitor being developed for the treatment of several autoimmune disorders with an IC50 of 43 nM. IC50 & Target: IC50: 43 nM (JAK1), 200 nM (JAK2) 了解更多
  17. Ombitasvir (ABT-267)

    Catalog No. A17624
    Quick View
    HCV NS5A inhibitor
    Ombitasvir is a potent inhibitor of the hepatitis C virus protein NS5A, with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a. 了解更多
  18. Linifanib (ABT-869)

    Catalog No. A10025
    Quick View
    VEGFR/PDGFR 抑制剂
    Linifanib (ABT-869)是一种结构新颖的有效RTK,VEGF和PDGF抑制剂,对人内皮细胞,PDGFR-β,KDR和CSF-1R的IC50分别为0.2、2、4和7 nM。 了解更多
  19. Paritaprevir (ABT-450)

    Catalog No. A17625
    Quick View
    HCV NS3/4A inhibitor
    Paritaprevir (ABT-450) is a potent non-structural protein 3/4A (NS3/4A) protease inhibitor with EC50s of 1 and 0.21 nM against HCV 1a and 1b, respectively. 了解更多

19 个项目

每页

设置升序顺序
Rewards