For research use only. Not for therapeutic Use.
CA-074 methyl ester (Cat No.:I001812) is a cell-permeable inhibitor of cathepsin B, a lysosomal cysteine protease. It is derived from the parent compound CA-074, but the addition of the methyl ester group enhances its cell permeability. CA-074 methyl ester selectively inhibits cathepsin B activity and has been widely used in research to investigate the role of cathepsin B in various biological processes. By inhibiting cathepsin B, CA-074 methyl ester can modulate cellular processes such as apoptosis, autophagy, inflammation, and tumor progression. Its specific inhibition of cathepsin B makes it a valuable tool for understanding the functions of this protease in both normal physiological and pathological conditions.
Catalog Number | I001812 |
CAS Number | 147859-80-1 |
Synonyms | methyl (2S)-1-[(2S)-3-methyl-2-[[(2S,3S)-3-(propylcarbamoyl)oxirane-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carboxylate |
Molecular Formula | C19H31N3O6 |
Purity | ≥95% |
Target | Cathepsin |
Solubility | 10 mM in DMSO |
Storage | Store at -20°C |
IUPAC Name | methyl (2S)-1-[(2S,3S)-3-methyl-2-[[(2S,3S)-3-(propylcarbamoyl)oxirane-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carboxylate |
InChI | InChI=1S/C19H31N3O6/c1-5-9-20-16(23)14-15(28-14)17(24)21-13(11(3)6-2)18(25)22-10-7-8-12(22)19(26)27-4/h11-15H,5-10H2,1-4H3,(H,20,23)(H,21,24)/t11-,12-,13-,14-,15-/m0/s1 |
InChIKey | XGWSRLSPWIEMLQ-YTFOTSKYSA-N |
SMILES | CCCNC(=O)[C@@H]1[C@H](O1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N2CCC[C@H]2C(=O)OC |
Reference | <p style=/line-height:25px/> <br>[2]. Patel N, et al. CA-074Me compound inhibits osteoclastogenesis via suppression of the NFATc1 and c-FOS signaling pathways. J Orthop Res. 2015 Oct;33(10):1474-86. <br>[3]. Zhang L, et al. Treatment with CA-074Me, a Cathepsin B inhibitor, reduces lung interstitial inflammation and fibrosis in a rat model of polymyositis. Lab Invest. 2015 Jan;95(1):65-77. <br>[4]. Cho K, et al. CA-074Me, a cathepsin B inhibitor, decreases APP accumulation and protects primary rat cortical neurons treated with okadaic acid. Neurosci Lett. 2013 Aug 26;548:222-7. </p> |