“ab fubinaca”的搜索结果

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  1. TAS-116

    Catalog No. A20987
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    HSP90??/HSP90?? inhibitor
    TAS-116 is an oral bioavailable, ATP-competitive, highly specific HSP90α/HSP90β inhibitor (Kis of 34.7 nM and 21.3 nM, respectively) without inhibiting other HSP90 family proteins such as GRP94. TAS-116 demonstrates less ocular toxicity. 了解更多
  2. MF-438

    Catalog No. A20963
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    SCD1 inhibitor
    MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with an EC50 of 2.3 nM for rSCD1. 了解更多
  3. CP-640186 hydrochloride

    Catalog No. A21808
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    ACC inhibitor
    CP-640186 hydrochloride is a potent and cell-permeable Acetyl-CoA carboxylase (ACC) inhibitor with IC50s of 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively. 了解更多
  4. VP3.15 dihydrobromide

    Catalog No. A21789
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    PDE7/GSK3 inhibitor
    VP3.15 dihydrobromide is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE)7- glycogen synthase kinase (GSK)3 inhibitor, with IC50s of 1.59 μM and 0.88 μM for PDE7 and GSK-3, respectively. 了解更多
  5. SHP099 hydrochloride

    Catalog No. A21762
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    SHP2 inhibitor
    SHP099 hydrochloride is a potent, selective and orally available SHP2 inhibitor with an IC50 of 70 nM. 了解更多
  6. BMS-654457

    Catalog No. A21704
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    Factor XIa (FXIa) inhibitor
    BMS-654457 is a small-molecule, reversible inhibitor of factor XIa (FXIa), binding with human and rabbit FXIa with Kis of 0.2 and 0.42 nM, respectively. 了解更多
  7. HS80

    Catalog No. A21615
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    FASN inhibitor
    HS-80 is an enantiomer of Fasnall, which is a selective fatty acid synthase (FASN) inhibitor. HS-80 is able to inhibit the incorporation of tritiated acetate into lipids with an IC50 of 7.13 μM. 了解更多
  8. CVT-12012

    Catalog No. A21447
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    SCD inhibitor
    CVT-12012 is a potent and orally bioavailable stearoyl-coA desaturase (SCD) inhibitor, with IC50s of 38 nM, 6.1 nM for rat microsomal and human HEPG2, respectively. 了解更多
  9. Rasagiline 13C3 mesylate racemic

    Catalog No. A21350
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    Monoamine oxidase inhibitor
    Rasagiline 13C3 mesylate racemic is the deuterium labeled Rasagiline, which is an irreversible inhibitor of monoamine oxidase. 了解更多
  10. Lazabemide

    Catalog No. A21270
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    MAO-B inhibitor
    Lazabemide(Ro 19-6327) is selective, reversible monoamine oxidase B (MAO-B) inhibitor (IC50 values are 0.03 and > 100 μM for MAO-B and MAO-A respectively). 了解更多
  11. Edoxaban

    Catalog No. A18015
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    factor Xa (FXa) inhibitor
    Edoxaban(DU-176) is an oral factor Xa (FXa) inhibitor in clinical development for stroke prevention. 了解更多
  12. TVB-3664

    Catalog No. A18829
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    FASN inhibitor
    TVB-3664 is an orally available, reversible, potent, selective and highly bioavailable fatty acid synthase (FASN) inhibitor, with IC50 values of 18 nM and 12 nM for human and mouse cell palmitate synthesis, respectively. TVB-3664 significantly reduces tubulin palmitoylation and mRNA expression. 了解更多
  13. HSP27 inhibitor J2

    Catalog No. A18874
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    HSP27 inhibitor
    HSP27 inhibitor J2 (J2) is a HSP27 inhibitor, which significantly induces abnormal HSP27 dimer formation and inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function thereof. 了解更多
  14. 2-Hydroxy atorvastatin calcium salt

    Catalog No. A18971
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    HMG-CoA reductase inhibitor
    2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt. Atorvastatin is a potent HMG-CoA reductase inhibitor with an IC50 value of 8 nM. 了解更多
  15. ND-646

    Catalog No. A20079
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    ACC inhibitor
    ND-646 is an orally bioavailable and steric inhibitor of acetyl-CoA carboxylase (ACC) with IC50s of 3.5 nM and 4.1 nM for recombinant hACC1 and hACC2, respectively. 了解更多
  16. A939572

    Catalog No. A13298
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    SCD1 inhibitor
    A939572 is a potent, and orally bioavailable stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 values of <4 nM and 37 nM for mSCD1 and hSCD1, respectively. 了解更多
  17. VP3.15

    Catalog No. A18538
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    dual PDE7/GSK-3 inhibitor
    VP3.15 is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE)7- glycogen synthase kinase (GSK)3 inhibitor, with IC50s of 1.59 μM and 0.88 μM for PDE7 and GSK-3, respectively. VP3.15 has neuroprotective and neuroreparative activities, thus as potential combined anti-inflammatory and pro-remyelinating therapies for multiple sclerosis (MS). 了解更多
  18. Col003

    Catalog No. A18573
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    Hsp47 inhibitor
    Col003 is a potent inhibitor of Hsp47, competitively binds to the collagen binding site on Hsp47 (IC50, 1.8 μM), and inhibits collagen secretion by destabilizing the collagen triple helix. 了解更多
  19. TVB-3166

    Catalog No. A18763
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    FASN inhibitor
    TVB-3166 is an orally-available, reversible, potent, and selective FASN inhibitor, inducing apoptosis, inhibiting anchorage-independent cell growth under lipid-rich conditions, and inhibiting in-vivo xenograft tumor growth. 了解更多
    • 最新产品

    BAY-876

    Catalog No. A17216
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    GLUT1 抑制剂
    BAY-876 is a potent and Selective GLUT1 Inhibitor. BAY-876 showed good metabolic stability in?vitro and high oral bioavailability in?vivo. 了解更多
  20. Edoxaban tosylate

    Catalog No. A15076
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    Factor Xa 抑制剂
    Edoxaban tosylate是临床预防卒中的口服Xa(FXa)抑制剂。 了解更多
  21. Choline Fenofibrate

    Catalog No. A15044
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    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
  22. ABT-046

    Catalog No. A14984
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    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
  23. 5-R-Rivaroxaban

    Catalog No. A14979
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    Factor Xa 抑制剂
    5-R-Rivaroxaban是利伐沙班的(R)对映异构体。利伐沙班是一种新型的口服直接Xa因子抑制剂,在晚期开发中用于预防和治疗血栓栓塞性疾病。 了解更多
  24. Edoxaban (tosylate Monohydrate)

    Catalog No. A14317
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    Factor Xa 抑制剂
    Edoxaban (tosylate Monohydrate)是选择性Factor Xa抑制剂,Ki为0.561 nM。 了解更多
  25. ABT333

    Catalog No. A13878
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    NS5B 抑制剂
    ABT333是NS5B非核苷聚合酶抑制剂。 了解更多
  26. Betrixaban

    Catalog No. A12518
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    FXa 抑制剂
    Betrixaban是一种抗凝血药,可作为直接Xa因子抑制剂。它具有强大的,口服活性和对因子Xa的高度选择性,由于其低hERG亲和力而从一组相似的化合物中选择。 了解更多
  27. ABT

    Catalog No. A13361
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    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
  28. Letaxaban (TAK-442)

    Catalog No. A12871
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    factor Xa 抑制剂
    Letaxaban (TAK-442)是一种有效的,选择性的,口服活性的Xa抑制剂,是一种四氢嘧啶-2(1H)-衍生物。TAK-442在贫血小板的人[半最大抑制浓度(IC(50)):53 nM,TAK-442]和大鼠(IC(50):32 nM,TAK-442)血浆中抑制内源性FXa活性。 了解更多
  29. Razaxaban

    Catalog No. A12870
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    factor Xa 抑制剂
    Razaxaban是凝血因子Xa的选择性,有效和口服生物利用抑制剂。 了解更多
  30. Crisaborole (AN2728)

    Catalog No. A12776
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    PDE4 抑制剂?
    AN2728是一种局部给药的含硼抗炎化合物,可抑制PDE4活性,从而抑制TNFalpha,IL-12,IL-23和其他细胞因子的释放。抑制PDE4的 IC50 值为0.49 μM。 了解更多
  31. Otamixaban (FXV 673)

    Catalog No. A11517
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    factor Xa 抑制剂
    Otamixaban (FXV 673)是一种静脉内直接因子Xa抑制剂。 了解更多
  32. Clarithromycin

    Catalog No. A10225
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    cytochrome P4503A4 抑制剂
    Clarithromycin是一种大环内酯类抗生素。它通过干扰细菌的蛋白质合成来防止细菌生长。 了解更多
  33. Fludarabine (Fludara)

    Catalog No. A10396
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    STAT 抑制剂
    Fludarabine或fludarabine(fludara)是一种用于治疗血液恶性肿瘤(血细胞癌,如白血病和淋巴瘤)的化疗药物。Fludarabine通过干扰核糖核苷酸还原酶和DNA聚合酶来抑制DNA合成。它对分裂细胞和静止细胞都有活性。 了解更多
  34. Rivaroxaban (Xarelto)

    Catalog No. A10800
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    Factor Xa 抑制剂
    Rivaroxaban (Xarelto)是一种Factor Xa的直接抑制剂,无细胞试验中Ki和IC50分别为0.4 nM和0.7 nM。 了解更多
  35. Methotrexate (Abitrexate)

    Catalog No. A10021
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    DHFR 抑制剂
    Methotrexate (Abitrexate)是一种抑制胸苷酸合成酶和从头嘌呤合成的细胞毒剂。 了解更多
  36. Abiraterone Acetate (CB7630)

    Catalog No. A11058
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    CYP17 抑制剂
    Abiraterone Acetate是Abiraterone的醋酸盐形式,是一种甾体类细胞色素CYP17抑制剂。 了解更多
  37. Abiraterone (CB-7598)

    Catalog No. A10020
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    CYP17 抑制剂
    Abiraterone (CB-7598)是一种有效CYP17抑制剂,20裂合酶(CYP17A1)。 了解更多
  38. Decitabine

    Catalog No. A10292
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    DNA Methyltransferase 抑制剂
    Decitabine是一种次甲基化剂,它通过抑制DNA甲基转移酶来使DNA次甲基化。 了解更多
  39. Apixaban (BMS-562247-01)

    Catalog No. A10082
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    Factor Xa 抑制剂
    Apixaban (BMS-562247-01)是一种抗凝剂,用于预防静脉血栓栓塞和静脉血栓栓塞事件。 了解更多

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