10
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10924 | Cysteine protease inhibitor-2 | Cysteine Protease | |
Cysteine protease inhibitor 2 is a cysteine protease inhibitor. Cysteine protease inhibitor 2 inhibited DCT116 and PC3 cells with GI50 values of 6.5 μM and 4.4 μM, respectively. | |||
T7451 | 2-Cyanopyrimidine | 2-cyano-Pyrimidine | Cysteine Protease |
2-Cyanopyrimidine (m-Hydroxyphenylpropionic acid) is inhibitor of cathepsin K(IC50 : 170 nM) | |||
T9458 | PF-00835231 | SARS-CoV | |
PF-00835231 is a CoV-2 cysteine 3C-like protease (3CLpro) inhibitor, with IC50s of 0.27 nM and 4 nM for SARS CoV-2 and SARS CoV-1 3CLpro, respectively.PF-00835231 is the active compound of the first anti-3CLpro regimen i... | |||
T80542 | Z-Leu-Leu-Leu-fluoromethyl ketone | Z-LLL-FMK | |
Z-Leu-Leu-Leu-fluoromethyl ketone (Z-LLL-FMK) functions as a cysteine protease inhibitor and has been shown to impede SARS infection. Furthermore, it affords protection to mice when challenged with T. crassiceps [1] [2]. | |||
T64159 | Cathepsin K inhibitor 2 | ||
Cathepsin K inhibitor 2 is a potent inhibitor of cathepsin K. Cathepsin K (Cat K) is a cysteine protease expressed under the control of the CTSK gene, which is closely related to osteoporosis and hydrolyses collagen. cat... | |||
T63537 | SARS-CoV-2 3CLpro-IN-1 | ||
SARS-CoV-2 3CLpro-IN-1 (Compound 14c) is a highly potent inhibitor specifically designed to target and inhibit the activity of SARS-CoV-2 3CL pro, which is a cysteine-protease found in the main coronaviruses. This partic... | |||
T63760 | 3CPLro-IN-2 | ||
3CPLro-IN-2 is a potent, orally active inhibitor of SARS-CoV-2 3CLpro (IC50: 1.55 μM, Ki: 6.09 μM). 3-Chymotrypsin-like cysteine protease (3CLpro) is an essential protein for viral replication and is a potential drug tar... | |||
T62479 | 3CPLro-IN-1 | ||
3CPLro-IN-1 (compound A17) is a potent, orally active inhibitor of SARS-CoV-2 3CLpro (IC50: 5.65 μM). 3-Chymotrypsin-like cysteine protease (3CLpro), a protein essential for viral replication, is an attractive drug targe... | |||
T78119 | Z-L(D-Val)G-CHN2 | HSV | |
Z-L(D-Val)G-CHN2, an isoform of Z-LVG-CHN2, serves as a cell-permeable and irreversible inhibitor of cysteine proteinase. This tripeptide derivative emulates a segment of the human cysteine proteinase-binding center and ... | |||
T35802 | ML-345 | ||
Insulin-degrading enzyme (IDE) is a thiol-sensitive zinc-metallopeptidase that acts as the major insulin-degrading protease in vivo, mediating the termination of insulin signaling. [1] In addition to regulating insulin a... |