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)

  • GC14435 structure
    GC14435Zileuton sodium
    CAS: 118569-21-4

    A reversible inhibitor of 5-lipoxygenase

  • GC14441 structure
    GC14441SW033291
    CAS: 459147-39-8
    纯度: >98.50% / >99.00% / >98.00%

    SW033291是15-羟基前列腺素脱氢酶(15-PGDH)的小分子抑制剂,15-PGDH是一种催化PGE2氧化和失活的酶。

  • GC14502 structure
    GC14502AEBSF.HCl
    CAS: 30827-99-7
    纯度: >99.50% / >98.50% / >98.00% / >99.00%

    AEBSF.HCl是丝氨酸蛋白酶广谱的不可逆的抑制剂,可抑制胰凝乳蛋白酶,激肽释放酶,纤溶酶,凝血酶,胰蛋白酶和相关的溶栓酶等。

  • GC14511 structure
    GC14511All-trans Retinal
    CAS: 116-31-4
    纯度: >98.00%

    All-trans Retinal 是一种具有活性的vitamin A aldehyde,对CRBP-I和CRBP-II蛋白的K d 值分别为50nM和90nM。

  • GC14533 structure
    GC14533Kynurenic acid
    CAS: 492-27-3
    纯度: >99.00% / >98.00%

    Kynurenic acid 是一种内源性色氨酸代谢物,是一种针对 NMDA、谷氨酸、α7 烟碱乙酰胆碱受体的广谱拮抗剂。

  • GC14547 structure
    GC14547Quinolinic acid
    CAS: 89-00-9
    纯度: >99.00%

    An excitotoxic agonist at NMDA receptors

  • GC14549 structure
    GC145493-Hydroxyphenylacetic acid
    CAS: 621-37-4

    A phenolic acid with diverse biological activities

  • GC14573 structure
    GC14573Xylose
    CAS: 25990-60-7
    纯度: >98.00%

    木糖是有机合成的中间体。

  • GC14727 structure
    GC14727CCCP
    CAS: 555-60-2
    纯度: >98.00% / >99.50%

    Carbonylcyanide-3-chlorophenylhydrazone (CCCP) 是一种质子载体,可导致线粒体内膜中的质子梯度解偶联,从而抑制 ATP 合成速率。

  • GC14751 structure
    GC14751Malotilate
    CAS: 59937-28-9
    纯度: >99.50%

    A hepatoprotective agent

  • GC14757 structure
    GC14757AGI-6780
    CAS: 1432660-47-3
    纯度: >98.00%

    A potent, selective inhibitor of mutant IDH2

  • GC14762 structure
    GC14762Palifosfamide
    CAS: 31645-39-3

    An active metabolite of ifosfamide

  • GC14776 structure
    GC14776EC 144
    CAS: 911397-80-3

    EC 144 是一种有效的选择性热休克蛋白 90 (Hsp90) 抑制剂,IC50 为 1.1 nM。 EC 144 抑制肿瘤生长并导致部分肿瘤消退。 EC 144 具有研究癌症疾病的潜力。

  • GC14780 structure
    GC14780Oseltamivir acid
    CAS: 187227-45-8
    纯度: >98.50% / >98.00%

    A neuraminidase inhibitor and antiviral

  • GC14786 structure
    GC14786P32/98 (hemifumarate)
    CAS: 251572-86-8

    A DPP IV inhibitor

  • GC14816 structure
    GC14816L-Adrenaline
    CAS: 51-43-4
    纯度: >99.50% / >98.00%

    An adrenergic receptor agonist

  • GC14827 structure
    GC14827Linagliptin (BI-1356)
    CAS: 668270-12-0
    纯度: >99.50%

    A potent DPP-4 inhibitor

  • GC14843 structure
    GC14843Serotonin HCl
    CAS: 153-98-0
    纯度: >99.50% / >98.00%

    Serotonin HCl是一种神经递质,是介导人体多种中枢和外周功能的关键信使。

  • GC14847 structure
    GC14847Psoralidin
    CAS: 18642-23-4
    纯度: >98.00%

    A furanocoumarin with anti-cancer activity

  • GC14851 structure
    GC14851Vidofludimus
    CAS: 717824-30-1
    纯度: >98.50%

    An immunosuppressive drug that inhibits DHODH

  • GC14930 structure
    GC14930Benzbromarone
    CAS: 3562-84-3
    纯度: >99.50%

    An inhibitor of URAT1

  • GC14943 structure
    GC14943Hypotaurine
    CAS: 300-84-5
    纯度: >99.50% / >98.00%

    Hypotaurine是牛磺酸生物合成的前体,是甘氨酸受体(glycine receptor)的内源性抑制性氨基酸。

  • GC14953 structure
    GC14953Spermine
    CAS: 71-44-3
    纯度: >99.00% / >97.00%

    A natural polyamine

  • GC14954 structure
    GC14954L-Canaline
    CAS: 496-93-5
    纯度: >95.00%

    A natural inhibitor of aminotransferases