| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V73051 | ABP 25 | 2965359-45-7 | ABP 25 is an activity-based probe for imaging cathepsin K with good potency and selectivity. |
|
V73052 | Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2 | 400716-78-1 | Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2 is a cathepsin D substrate for cathepsin D FRET Determination. |
|
V110351 | AM9053 | 157469-21-1 | AM9053 is a highly selective, potent, slow-acting, and reversible inhibitor of N-acylethanolamine amidase (NAAA) (IC50 = 30 nM). |
|
V3381 | ARN14974 | 1644158-57-5 | ARN14974 (ARN-14974), a benzoxazolone carboxamide analog, is a novel and potent inhibitor of acid ceramidase with IC50of 79 nM. |
|
V73055 | Cathepsin C-IN-3 | 2825567-71-1 | Cathepsin C-IN-3 (compound SF11) is a potent inhibitor of cathepsin C (Cat C) with IC50 of 61.79 nM. |
|
V73056 | Cathepsin C-IN-4 | 2825567-86-8 | Cathepsin C-IN-4 (compound SF27) is a potent inhibitor of cathepsin C (Cat C) with IC50 of 65.6 nM. |
|
V73034 | Cathepsin G Inhibitor I | 429676-93-7 | Cathepsin G Inhibitor I is a potent, selective, reversible, competitive, non-peptide inhibitor of cathepsin G. |
|
V73922 | D-erythro-MAPP (De-MAPP) | 143492-38-0 | D-erythro-MAPP (De-MAPP) is an inhibitor (blocker/antagonist) of ceramidase with an in vitro IC50 of 1-5 μM. |
|
V73035 | RO5461111 | 1252637-46-9 | RO5461111 is a specific, orally bioactive Cathepsin S antagonist (IC50= 0.4 nM, human Cathepsin S; 0.5 nM, murine Cathepsin S). |
|
V145206 | Sphingolipid E | 110483-07-3 | Sphingolipid E is a synthetic pseudoceramide sphingolipid, similar to type II ceramides, and has a metastable layered structure. |
|
V73050 | Z-Phe-Arg-pNA | 117761-01-0 | Z-Phe-Arg-pNA is a substrate of cathepsin L. |
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