T6738 |
Z-FA-FMK
|
197855-65-5
|
99.43%
|
|
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
|
T9710 |
Dazcapistat
|
2221010-42-8
|
99.41%
|
|
Dazcapistat is a potent calpain inhibitor, with IC50s of <3 μM for calpain 1, calpain 2 and calpain 9, respectively.
|
T12051 |
MIV-247
|
1352817-76-5
|
99.31%
|
|
MIV-247 is a selective and potent inhibitor of cathepsin S (Kis 2.1, 4.2, and 7.5 nM for human, mouse, and wild monkey cathepsin S, respectively), which attenuat...
|
T65868 |
Z-Lys-OH
|
2212-75-1
|
99.11%
|
|
Z-Lys-OH is a competitive inhibitor of papain, a lysine derivative.
|
T15303 |
FMK 9a
|
1955550-51-2
|
98.97%
|
|
FMK 9a is an irreversible inhibitor of ATG4B with IC50 values of 80 and 73 nM in the TR-FRET and cellular-based LRA assays.
|
TN1249 |
3-Epiursolic acid
|
989-30-0
|
98.81%
|
|
3-Epiursolic acid may have antiinflammatory activity, it shows inhibition on Cathepsins L (catL), the IC50 value of 6.5 μM, cathepsins L (catL) and B play an imp...
|
T27695 |
JTE-607
|
188791-09-5
|
98.72%
|
|
JTE-607 is a cytokine production inhibitor. JTE-607 induces apoptosis accompanied by an increase in p21waf1/cip1 in acute myelogenous leukemia cells.
|
T27730 |
KGP94
|
1131456-28-4
|
98.52%
|
|
KGP94 is an inhibitor of cysteine protease Cathepsin L(CTSL).
|
T21616 |
L-006235
|
294623-49-7
|
98.38%
|
|
L-006235 is a potent and reversible inhibitor of cathepsin K with IC50 of 0.25 nM.
|
T19384 |
Isovalerylcarnitine
|
31023-24-2
|
98.24%
|
|
Isovalerylcarnitine (3-methylbutyrylcarnitine) is a small molecule compound produced by the catabolism of L-leucine and the accumulation of isovaleric acid. Isov...
|
T20626 |
Esomeprazole
|
119141-88-7
|
98.20%
|
|
Esomeprazole is the S-isomer of omeprazole, inhibits the lysosomal cysteine protease legumain to prevent cancer metastasis. Esomeprazole is a proton pump inhibit...
|
T12909 |
SID 26681509
|
958772-66-2
|
98.16%
|
|
SID 26681509 is a selective, reversible and competitive human cathepsin L inhibitor (IC50 of 56 nM).
|
T60150 |
(1S,2R)-Alicapistat
|
2221010-57-5
|
98.05%
|
|
(1S,2R)-Alicapistat ((1S,2R)-ABT-957) is a highly efficient, orally active compound that selectively inhibits human calpains 1 and 2, with promising implications...
|
T6564 |
Leupeptin Hemisulfate
|
103476-89-7
|
98.00%
|
|
Leupeptin hemisulfate is a protease inhibitor with cell membrane-permeable, reversible, competitive, and oral activities. Leupeptin hemisulfate inhibits the acti...
|
T6583 |
MG-101
|
110044-82-1
|
98%
|
|
MG-101 (Calpain inhibitor I) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
|
T2493 |
PD 151746
|
179461-52-0
|
98%
|
|
PD151746 is a calpain inhibitor with a 20-fold selectivity for u-calpain (Ki = 0.26 ± 0.03 μM) over m-calpain (Ki = 5.33 ± 0.77 μM). Its IC50 values are 0.26 ± 0...
|
T3088 |
N-Ethylmaleimide
|
128-53-0
|
98%
|
|
N-Ethylmaleimide (NEM) is a sulfhydryl reagent that is widely used in experimental biochemical studies.
|
T7451 |
2-Cyanopyrimidine
|
14080-23-0
|
98%
|
|
2-Cyanopyrimidine (m-Hydroxyphenylpropionic acid) is inhibitor of cathepsin K(IC50 : 170 nM)
|
TQ0116 |
LY 3000328
|
1373215-15-6
|
97.83%
|
|
LY 3000328 (Cathepsin S inhibitor) is a potent, highly selective Cathepsin S (Cat S) inhibitor (IC50s: 7.7 and 1.67 nM for hCat S and mCat S).
|
T21509 |
CA 074
|
134448-10-5
|
97.80%
|
|
CA 074 is a potent inhibitor of cathepsin B with a Ki value of 2 to 5 nM.CA 074 inhibits ischemic hippocampal neuronal death in primates and attenuates retinopat...
|