| Cat. No. |
Product Name |
Information |
| PC-73032 |
K777
Cathepsin L inhibitor
|
K777 (K11777, S-001, SLV213) is a highly potent, irreversible, covalent inhibitor of mammalian cathepsin L and other cysteine proteases of clan CA. |
| PC-72382 |
JNJ-39641160
Cathepsin S inhibitor
|
JNJ-39641160 (JNJ39641160) is a peripherally restricted, non-covalent, potent, selective, orally-available Cathepsin S (CatS) inhibitor with Ki of 38 nM (hCatS). |
| PC-38309 |
Z-Arg-Lys-AOMK
Cathepsin B inhibitor
|
Z-Arg-Lys-AOMK is a potent, selective, irreversible neutral pH 7.2 inhibitor of Cathepsin B with IC50 of 13 nM, >100-fold higher potent than at pH 4.6 (IC50=1,830 nM). |
| PC-38292 |
BI-1915
Cathepsin S inhibitor
|
BI-1915 (BI 1915) is a highly potent, selective inhibitor of Cathepsin S (CatS) with IC50 of 17 nM for in vitro use, no significant inhibition on Cathepsin L/K/B (IC50>10 uM). |
| PC-38291 |
BI-1124
Cathepsin S inhibitor
|
BI-1124 (BI 1124) is a highly potent, selective inhibitor of Cathepsin S (CatS) with IC50 of 7 nM, >40-fold selectivity over Cathepsin L/K/B. |
| PC-35163 |
MIV-711
Cathepsin K inhibitor
|
MIV-711 (MIV711, MV076159) is a potent, selective cathepsin K inhibitor with Ki of 0.98 nM, displays >1300-fold versus the other human cathepsins. |
| PC-35082 |
Cathepsin B inhibitor RC1
Cathepsin B inhibitor
|
Cathepsin B inhibitor RC1 is a small-molecule that blocks the process of anthrax lethal toxin (LT) cytotoxicity, inhibits enzymatic activity of host cathepsin B that mediates the escape of toxins into the cytoplasm from late endosomes. |
| PC-63161 |
AZD5248
DPP-1/CatC inhibitor
|
AZD5248 is a potent, selective, first generation, oral inhibitor of dipeptidyl peptidase 1 (DPP1, cathepsin C, CatC). |
| PC-62965 |
VEL-0230
Cathepsin inhibitor
|
VEL-0230 (NC-2300) is a potent, selective cysteine Cathepsins inhibitor with IC50 of 284, 34.5 and 186 nM for Cat B, K and S, respectively. |
| PC-62964 |
L 873724
Cathepsin K inhibitor
|
L 873724 is a potent and selective non-basic cathepsin K inhibitor with IC50 of 0.2 nM, shows no significant potency against Cat B, L, and S (IC50= 5239, 264, and 178 nM). |
| PC-62962 |
Relacatib
Cathepsin K inhibitor
|
Relacatib (SB-462795, GSK-462795) is a potent and orally bioavailable small molecule cathepsin inhibitor with Ki of 41, 68 and 53 pM for cathepsin K, L and V, respectively. |
| PC-62961 |
MK-0674
Cathepsin K inhibitor
|
MK-0674 (MK 0674) is a potent, selective, reversible and orally active cathepsin K inhibitor with IC50 of 1 nM. |
