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Cathepsin

Cathepsin

Cathepsin related products

Structure Cat No. Product Name CAS No. Product Description
Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2 acetate V109007 Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2 acetate Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2 acetate is a cathepsin D substrate that can be used for the detection of cathepsin D FRET.
Anti-inflammatory agent 113 V129061 Anti-inflammatory agent 113 Anti-inflammatory agent 113 is a cathepsin L (CTSL) inhibitor with anti-inflammatory activity and a CTSL IC50 value of 5.52 μM.
Cathepsin D degrader 1 V131137 Cathepsin D degrader 1 Cathepsin D degrader 1 is an orally effective anti-hepatic fibrosis compound that targets cathepsin D.
Cathepsin K inhibitor 7 V101025 Cathepsin K inhibitor 7 Cathepsin K inhibitor 7 (Compound 7) is a Cathepsin K inhibitor with a pKi value of 7.3 for CatK.
Cathepsin K-IN-8 V119350 Cathepsin K-IN-8 501126-27-8 Cathepsin K-IN-8 (Examples 6-60) is a cathepsin K inhibitor that can be used to study inflammation, rheumatoid arthritis, osteoarthritis, osteoporosis, and tumors.
CTSL/CAPN1-IN-1 V87358 CTSL/CAPN1-IN-1 CTSL/CAPN1-IN-1 (compound 14a) is an orally active CTSL and CAPN1 inhibitor with IC50 values of 3.34 nM and 375.1 nM, respectively.
E-64 HCl V3413 E-64 HCl E-64 HCl, the hydrochloride salt form of E-64, which isisolated from cultures of Aspergillus, is anovel, potent,irreversible and selective cysteine protease inhibitor with IC50 of 9 nM for papain.
GB111-NH2 hydrochloride V86026 GB111-NH2 hydrochloride
MK-0674 V4301 MK-0674 887781-62-6 MK-0674 is a novel, potent, orally bioavailable and selectivecathepsin Kinhibitor with anIC50of 0.4 nM.
PI3K-001 V142684 PI3K-001 PI3K-001 is a prodrug and antifibrotic drug sensitive to cathepsin B.
S2160 hydrochloride V144470 S2160 hydrochloride 38789-84-3 S2160 hydrochloride is a substrate for cathepsin B and can be used for the determination of cathepsin B by calorimetry.
SmCB1-IN-1 V88986 SmCB1-IN-1 SmCB1-IN-1 (Compound 2h) is an inhibitor of Schistosoma mansoni protease B1 (SmCB1) with Ki of 0.05 μM.
TB-9 V104024 TB-9 1415033-91-8 TB-9 is a Tasiamide B derivative and a potent inhibitor of cathepsin D, cathepsin E, and BACE1 with IC50 of 0.0783 nM, 0.724 nM, and 54.2 nM, respectively.
VK13 V146997 VK13 VK13 is a potent inhibitor of human cathepsin L (hCatL) with a Ki value of 0.55 nM, and also a potent inhibitor of SARS-CoV-2 3CLpro (3CL-PR) with a Ki value of 2.6 nM.
Y1693 V147216 Y1693 2812381-74-9 Y1693 is an orally effective RANKL inhibitor with a Kd value of 5.03 μM for hRANKL.
Z-Arg-Lys-AOMK V147297 Z-Arg-Lys-AOMK 2810056-57-4 Z-Arg-Lys-AOMK is a cathepsin B inhibitor that can cross the blood-brain barrier.
Z-FF-FMK (Z-Phe-Phe-FMK) V85555 Z-FF-FMK (Z-Phe-Phe-FMK) 105608-85-3
Z-Val-Val-Nle-diazomethylketone V147421 Z-Val-Val-Nle-diazomethylketone 155026-49-6 Z-Val-Val-Nle-diazomethylketone is a cathepsin S (CATS) inhibitor.
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