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CA-074

CAS No. : 134448-10-5

MCE 站：CA-074

产品活性：CA-074是组织蛋白酶B (cathepsin B) 的有效抑制剂， K_i 值为2 to 5 nM。

研究领域：Metabolic Enzyme/Protease

作用靶点：Cathepsin

In Vitro: CA-074 is a synthetic analogue of E-64, a natural peptidyl epoxide that irreversibly inhibits most known lysosomal cysteine proteinases, and is developed by means of rational drug design, exploiting the dipeptidylcarboxypeptidase activity of cathepsin B. CA-074 can be used to selectively inhibit cathepsin B within living cells, as long as the experimental conditions permit significant fluid-phase endocytosis of the drug. CA-074 inhibits cathepsin B with a K_i of 2 to 5 nM, whereas the initial K_is for cathepsin H and L are about 40-200 μM. CA-074 exhibits 10000-30000 times greater inhibitory effects on purified rat cathepsin B than on cathepsin H and L.

In Vivo: Intraperitoneally injection of compound CA-074 into rats potently and selectively inhibits cathepsin B activity. Intravenously administration of CA-074 immediately after the ischaemic insult saves 67% of CA1 neurons from delayed neuronal death on day 5 in eight monkeys undergoing 20 min brain ischaemia: the extent of inhibition is excellent in three of eight and good in five of eight monkeys.

相关产品：Covalent Screening Library Plus  |  Bioactive Compound Library Plus  |  Metabolism/Protease Compound Library  |  Anti-Cancer Compound Library  |  Peptidomimetic Library  |  Covalent Screening Library  |  Leupeptin hemisulfate  |  Aloxistatin  |  N-Ethylmaleimide  |  PMSF  |  E-64  |  CA-074 methyl ester  |  Calpeptin  |  Papain  |  LY 3000328  |  SID 26681509  |  LHVS  |  S130  |  VBY-825  |  E 64c  |  K777  |  Z-LVG-CHN2  |  Z-WEHD-FMK  |  JPM-OEt  |  LV-320  |  NSC 185058  |  2-Cyanopyrimidine  |  3-Epiursolic Acid  |  ONO-5334  |  Cysteine Protease inhibitor  |  Asperphenamate  |  ALLM  |  Aurantiamide acetate  |  Cathepsin D and E FRET Substrate

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