“AZ 960”的搜索结果

26 个项目

每页

设置降序顺序
  1. HCV-IN-3

    Catalog No. A20957
    Quick View
    HCV NS3/4a protein inhibitor
    HCV-IN-3 is a hepatitis C virus (HCV) NS3/4a protein inhibitor, with an IC50 of 20 μM, a Kd of 29 μM. 了解更多
  2. Vildagliptin dihydrate

    Catalog No. A21898
    Quick View
    DPP4 inhibitor
    Vildagliptin (LAF237 dihydrate;NVP-LAF 237 dihydrate) is a dipeptidyl peptidase 4 (DPP4) inhibitor that delays the degradation of glucagon-like peptide-1 (GLP-1). 了解更多
  3. Thrombin Inhibitor 2

    Catalog No. A21814
    Quick View
    thrombin inhibitor
    Thrombin Inhibitor 2 is a small molecule direct thrombin inhibitor, extracted from US8541580B2. Thrombin Inhibitor 2 has antithrombotic activity. 了解更多
  4. PSI-6206 13CD3

    Catalog No. A21782
    Quick View
    HCV NS5B polymerase inhibitor
    PSI-6206 13CD3 is the deuterium labeled PSI-6206. PSI-6206 is the deaminated derivative of PSI-6130, which is a potent and selective inhibitor of HCV NS5B polymerase. 了解更多
  5. AZD3839 free base

    Catalog No. A21606
    Quick View
    BACE1 inhibitor
    AZD3839 (free base) is a potent and selective BACE1 inhibitor with IC50 of 23.6 uM, about 14-fold selectivity over BACE2, also a β-secretase enzyme inhibitor. 了解更多
  6. Odiparcil

    Catalog No. A21584
    Quick View
    indirect thrombin inhibitor
    Odiparcil (SB-424323) is indirect thrombin inhibitor that exerts its anticoagulant effect through activation of antithrombin II (heparin cofactor II) . 了解更多
  7. Teneligliptin hydrobromide hydrate

    Catalog No. A21465
    Quick View
    DPP-4 inhibitor
    Teneligliptin hydrobromide hydrate is a potent chemotype prolylthiazolidine-based DPP-4 inhibitor, which competitively inhibits human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50s of approximately 1 nM. 了解更多
  8. β-Secretase Inhibitor IV

    Catalog No. A21346
    Quick View
    BACE-1 inhibitor
    β-Secretase Inhibitor IV is a potent, cell-active BACE-1 inhibitor with IC50s of 15.6 and 16.3nM under BACE-1 concentrations of 2 nM and 100 pM, respectively. 了解更多
  9. BMS-906024

    Catalog No. A21172
    Quick View
    gamma secretase inhibitor
    BMS-906024 is an oral and selective gamma secretase inhibitor (GSI) that is a small molecule Notch inhibitor. 了解更多
  10. Ixazomib citrate

    Catalog No. A18017
    Quick View
    20S proteasome inhibitor
    Ixazomib citrate (MLN9708) is a reversible inhibitor of the chymotrypsin-like proteolytic β5 site of the 20S proteasome with an IC50 of 3.4 nM and a Ki of 0.93 nM. 了解更多
  11. R-1479

    Catalog No. A11540
    Quick View
    HCV replication inhibitor
    R-1479 is a specific inhibitor of HCV replication in the HCV subgenomic replicon system (IC50=1.28 μM). 了解更多
  12. Mericitabine

    Catalog No. A11539
    Quick View
    HCV NS5B polymerase inhibitor
    Mericitabine (RG 7128; R-7128) is a nucleoside inhibitor of the HCV NS5B polymerase that acts as an RNA chain terminator and prevents elongation of RNA transcripts during replication. 了解更多
  13. Proteasome-IN-1

    Catalog No. A12254
    Quick View
    proteasome inhibitor
    Proteasome-IN-1 is a proteasome inhibitor extracted from patent WO 2013142376 A1. 了解更多
  14. Lanabecestat

    Catalog No. A12282
    Quick View
    BACE1 inhibitor
    Lanabecestat (AZD3293) is a potent, highly permeable, orally active and blood-brain barrier penetrating BACE1 inhibitor with a Ki of 0.4 nM. 了解更多
  15. MMP3 inhibitor 1

    Catalog No. A13185
    Quick View
    MMP-3 inhibitor
    MMP3 inhibitor 1 is a potent and highly selective MMP-3 inhibitor with an IC50 of 1 nM. 了解更多
  16. Voxilaprevir

    Catalog No. A12067
    Quick View
    HCV NS 3/4A protease inhibitor
    Voxilaprevir (GS-9857) is a fluorinated macrocyclic hepatitis C virus (HCV) nonstructural protein (NS) 3/4A protease inhibitor with potent in vitro antiviral activity against genotypes 1-6 HCV and broad coverage of NS3/4A protease polymorphisms. GS-9857 improves coverage against commonly encountered NS3 resistance-associated variants (RAVs). 了解更多
  17. BR351

    Catalog No. A18617
    Quick View
    MMP inhibitor
    BR351 is a brain penetrant MMP inhibitor with IC50s of 4, 2, 11, 50 nM for MMP2, MMP8, MMP9 and MMP13, respectively. 了解更多
  18. AZD7986

    Catalog No. A17095
    Quick View
    DPPI 抑制剂
    AZD7986,也称为INS 1007,是第二代可逆共价,有效和选择性DPP1抑制剂,潜在地可用于治疗慢性阻塞性肺疾病(COPD),其预测的人PK特性适用于每日一次人类给药。 了解更多
  19. AZ 10417808

    Catalog No. A15294
    Quick View
    Caspase-3 抑制剂
    AZ 10417808,caspase-3的选择性非肽抑制剂(Ki = 247 nM);相对于半胱氨酸蛋白酶1、2、6、7和8(Ki> 10 uM)显示的选择性> 40倍。 了解更多
  20. Alvelestat

    Catalog No. A12779
    Quick View
    neutrophil elastase 抑制剂
    Avelestat,也称为AZD9668,是可口服的,高度选择性neutrophil elastase (NE)抑制剂,IC50和Ki分别为12 nM和9.4 nM,其选择性超过其他丝氨酸蛋白酶至少600倍。 了解更多
  21. AZD3839

    Catalog No. A12825
    Quick View
    BACE1 抑制剂
    AZD3839是人类BACE1的有效选择性抑制剂,Ki为26.1 nM。 了解更多
  22. ONX-0914

    Catalog No. A12653
    Quick View
    Immunoproteasome 抑制剂
    ONX 0914是有效,选择性的免疫蛋白酶体亚基LMP7的抑制剂,在自身免疫性疾病(如类风湿性关节炎,炎性肠病和狼疮)中具有潜在的治疗应用。ONX 0914被设计为一种有效的免疫蛋白酶抑制剂,对组成型蛋白酶体的交叉反应最小。 了解更多
  23. Atazanavir

    Catalog No. A10097
    Quick View
    HIV Protease 抑制剂
    Atazanavir是一种氮杂肽及HIV-蛋白酶抑制剂,常与其他抗HIV药物结合,用于治疗HIV感染以及获得性免疫缺乏综合征。 了解更多
  24. Atazanavir sulfate (BMS-232632-05)

    Catalog No. A10096
    Quick View
    HIV Protease 抑制剂
    Atazanavir sulfate (BMS-232632-05)是蛋白酶抑制剂(PI)类的抗逆转录病毒药物。是一种高选择性的 HIV-1蛋白酶抑制剂。 了解更多
  25. YO-01027

    Catalog No. A11174
    Quick View
    γ-secretase 抑制剂
    YO-01027是一种二肽γ-secretase抑制剂,作用于APPL和Notch分裂, 无细胞试验中IC50分别为2.6 nM和2.9 nM,一种抗阿尔茨海默氏病药物。 了解更多
  26. MLN2238 (Ixazomib)

    Catalog No. A10600
    Quick View
    Proteasome 抑制剂
    MLN2238 (Ixazomib)是20S蛋白酶体抑制剂的有效可逆特异性β5位点,IC50值为3.4 nM。 了解更多

26 个项目

每页

设置降序顺序
Rewards