Proteases

Proteases(蛋白酶)

Proteases, also known as peptidases or proteolytic enzymes, consists of a large number of enzymes catalyzing the hydrolysis of peptide bonds and subsequently resulting in the degradation of protein substrates into amino acids. Proteases are involved in a wide range of human diseases, including cancer, neurodegenerative disorders, inflammatory diseases and cardiovascular diseases. Thus numerous proteases inhibitors (small molecules and proteins) have been identified to block activity of proteases. Proteases inhibitors can be classified into different types based on the class of proteases they inhibit through two general mechanisms, irreversible “trapping” reactions and reversible tight-binding reactions. Proteases inhibitors have been used as diagnostic or therapeutic agents for the treatment of proteases-related diseases.

研究方向

Proteases 相关产品(4079)

  • GC13467 structure
    GC13467PMPA (NAALADase inhibitor)
    CAS: 173039-10-6
    纯度: >98.00%

    A potent inhibitor of GCP II/NAALADase

  • GC13487 structure
    GC13487ARP 100
    CAS: 704888-90-4
    纯度: >99.00% / >98.00%

    A selective inhibitor of MMP-2

  • GC13673 structure
    GC13673BMS-708163 (Avagacestat)
    CAS: 1146699-66-2
    纯度: >98.00%

    A potent inhibitor of γ-secretase

  • GC13716 structure
    GC13716Lopinavir
    CAS: 192725-17-0
    纯度: >99.50% / >99.00%

    A potent HIV-1 protease inhibitor

  • GC13750 structure
    GC13750Doxycycline HCl
    CAS: 10592-13-9

    Doxycycline HCl 是一种抗生素,是一种具有口服活性的广谱金属蛋白酶 (MMP) 抑制剂。

  • GC14322 structure
    GC14322MPC-3100
    CAS: 958025-66-6

    An inhibitor of Hsp90

  • GC14523 structure
    GC14523GM 6001
    CAS: 142880-36-2
    纯度: >98.00%

    GM 6001 是一种广谱 MMP 抑制剂,可用于癌症和神经退行性疾病的研究,GM 6001对 MMP-1、2、3、8 和 9 的 Ki 值分别为 0.4、0.5、27、0.1和 0.2 nM。

  • GC14785 structure
    GC14785Alvelestat
    CAS: 848141-11-7
    纯度: >99.50%

    An inhibitor of neutrophil elastase

  • GC14870 structure
    GC14870OSMI-1
    CAS: 1681056-61-0
    纯度: >98.00% / >99.50%

    OSMI-1是一种O-GlcNAc转移酶(OGT)小分子抑制剂,不会显著影响其他糖基转移酶。

  • GC15066 structure
    GC15066Z-FA-FMK
    CAS: 197855-65-5
    纯度: >98.00%

    An inhibitor of cysteine proteases, including cathepsin B

  • GC15180 structure
    GC15180BIBR-1048
    CAS: 211915-06-9
    纯度: >99.50%

    A prodrug form of dabigatran

  • GC15390 structure
    GC15390Dabigatran etexilate mesylate
    CAS: 872728-81-9
    纯度: >98.00%

    A prodrug form of dabigatran

  • GC15493 structure
    GC15493Enalaprilat Dihydrate
    CAS: 84680-54-6
    纯度: >98.00%

    Enalaprilat Dihydrate是一种具有口服活性的血管紧张素转换酶(ACE)抑制剂,在体内可迅速水解为活性代谢物Enalaprilat,Enalaprilat通过抑制血管紧张素II的生成,有效舒张血管,降低血压,并减轻心脏负荷。

  • GC15561 structure
    GC15561MK-2048
    CAS: 869901-69-9

    MK-2048 是一种有效的整合酶和 INR263K 抑制剂,IC50 分别为 2.6 nM 和 1.5 nM。

  • GC15577 structure
    GC15577Bestatin hydrochloride
    CAS: 65391-42-6
    纯度: >99.50% / >99.00%

    Bestatin hydrochloride是氨基肽酶N(APN/CD13)抑制剂,其IC 50 值为14.9±3.4μM。

  • GC15760 structure
    GC15760Ramipril
    CAS: 87333-19-5
    纯度: >98.00%

    A prodrug from of ramiprilat

  • GC16293 structure
    GC16293BIBR 953 (Dabigatran, Pradaxa)
    CAS: 211914-51-1
    纯度: >98.50%

    A thrombin inhibitor

  • GC16316 structure
    GC16316Q-VD-OPh hydrate
    CAS: 1135695-98-5
    纯度: >99.50% / >97.00%

    Q-VD-OPh hydrate是一种广谱、可渗透细胞、高效且无毒的caspase抑制剂,对重组caspase1,3,8和9的IC 50 值在25-400nM范围内。

  • GC16530 structure
    GC16530Batimastat (BB-94)
    CAS: 130370-60-4
    纯度: >98.50% / >98.00%

    Batimastat (BB-94)是一种有效的广谱基质金属蛋白酶(MMPs)抑制剂,能够抑制MMP-1,MMP-2,MMP-9,MMP-7和MMP-3,IC 50 值分别为3nM,4nM,4nM,6nM和20nM。

  • GC16892 structure
    GC16892XL-888
    CAS: 1149705-71-4
    纯度: >99.50%

    An orally bioavailable Hsp90 inhibitor

  • GC16901 structure
    GC16901PSI-6206
    CAS: 863329-66-2
    纯度: >99.50%

    An inactive derivative of a HCV NS5B inhibitor

  • GC16966 structure
    GC16966VER 155008
    CAS: 1134156-31-2
    纯度: >99.50%

    VER 155008是一种强效的,源自腺苷的热休克蛋白70(Hsp70)家族抑制剂,对Hsp70、热休克同源蛋白70(Hsc70)和葡萄糖调节蛋白78(Grp78)的IC 50 值分别为0.5μM、2.6μM和2.6μM。

  • GC18004 structure
    GC18004MK-5172
    CAS: 1350514-68-9
    纯度: >99.50%

    MK-5172是一种丙型肝炎病毒(HCV)NS3/4a蛋白酶选择性抑制剂,对多种基因型及耐药变异株均具有广谱活性,并能抑制SARS-CoV-2 3CL蛋白酶活性。

  • GC18065 structure
    GC18065ZJ 43
    CAS: 723331-20-2

    ZJ 43 是一种有效的 NAAG 肽酶抑制剂,IC50 为 2.4 nM,Ki 为 0.8 nM。