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Cysteine Protease

Cysteine proteases, also known as thiol proteases, are enzymes that degrade proteins. These proteases share a common catalytic mechanism that involves a nucleophilic cysteine thiol in a catalytic triad or dyad.
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T6738 Z-FA-FMK 197855-65-5 99.43%
Z-FA-FMK
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
T9710 Dazcapistat 2221010-42-8 99.41%
Dazcapistat
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
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
Z-Lys-OH is a competitive inhibitor of papain, a lysine derivative.
T15303 FMK 9a 1955550-51-2 98.97%
FMK 9a
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
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
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
KGP94 is an inhibitor of cysteine protease Cathepsin L(CTSL).
T21616 L-006235 294623-49-7 98.38%
L-006235
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
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
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
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)-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
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
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%
PD 151746
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
N-Ethylmaleimide (NEM) is a sulfhydryl reagent that is widely used in experimental biochemical studies.
T7451 2-Cyanopyrimidine 14080-23-0 98%
2-Cyanopyrimidine
2-Cyanopyrimidine (m-Hydroxyphenylpropionic acid) is inhibitor of cathepsin K(IC50 : 170 nM)
TQ0116 LY 3000328 1373215-15-6 97.83%
LY 3000328
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
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...
Z-FA-FMK
T6738
Z-FA-FMK can irreversibly inhibit cysteine protease and also inhibit effector caspases.
Dazcapistat
T9710
Dazcapistat is a potent calpain inhibitor, with IC50s of <3 μM for calpain 1, calpain 2 and calpain 9, respectively.
MIV-247
T12051
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...
Z-Lys-OH
T65868
Z-Lys-OH is a competitive inhibitor of papain, a lysine derivative.
FMK 9a
T15303
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.
3-Epiursolic acid
TN1249
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...
JTE-607
T27695
JTE-607 is a cytokine production inhibitor. JTE-607 induces apoptosis accompanied by an increase in p21waf1/cip1 in acute myelogenous leukemia cells.
KGP94
T27730
KGP94 is an inhibitor of cysteine protease Cathepsin L(CTSL).
L-006235
T21616
L-006235 is a potent and reversible inhibitor of cathepsin K with IC50 of 0.25 nM.
Isovalerylcarnitine
T19384
Isovalerylcarnitine (3-methylbutyrylcarnitine) is a small molecule compound produced by the catabolism of L-leucine and the accumulation of isovaleric acid. Isov...
Esomeprazole
T20626
Esomeprazole is the S-isomer of omeprazole, inhibits the lysosomal cysteine protease legumain to prevent cancer metastasis. Esomeprazole is a proton pump inhibit...
SID 26681509
T12909
SID 26681509 is a selective, reversible and competitive human cathepsin L inhibitor (IC50 of 56 nM).
(1S,2R)-Alicapistat
T60150
(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...
Leupeptin Hemisulfate
T6564
Leupeptin hemisulfate is a protease inhibitor with cell membrane-permeable, reversible, competitive, and oral activities. Leupeptin hemisulfate inhibits the acti...
MG-101
T6583
MG-101 (Calpain inhibitor I) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
PD 151746
T2493
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...
N-Ethylmaleimide
T3088
N-Ethylmaleimide (NEM) is a sulfhydryl reagent that is widely used in experimental biochemical studies.
2-Cyanopyrimidine
T7451
2-Cyanopyrimidine (m-Hydroxyphenylpropionic acid) is inhibitor of cathepsin K(IC50 : 170 nM)
LY 3000328
TQ0116
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).
CA 074
T21509
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...
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TargetMol