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 About 28 results found for searched term "Cathepsin G" (0.127 seconds)

Cat.No.  Name Target
M52652 Cathepsin G Cathepsin
Cathepsin G acts as a potent agonist of human platelet activation leading to their aggregation., and can be used for screening of relevant inhibitors.
M53632 Cathepsin G(1-5) Antibiotic
Cathepsin G(1-5) is an antimicrobial peptide that can be found in the clostripain-digested cathepsin G mixture.
M1985 Odanacatib Cathepsin
MK-0822
Odanacatib (MK-0822) is a potent and reversible covalent inhibitor of CathepsinK (CatK) with an IC50 of 0.2 nM/1 nM for human/rabbit cathepsin B, L, and S and is highly selective.
M2600 Balicatib Cathepsin
AAE-581
Balicatib is a potent and selective inhibitor of cathepsin K; 10-100-fold more potent in cell-based enzyme occupancy assays than against cathepsin B, L, and S.
M10412 Val-cit-PAB-OH ADC Linker
Val-cit-PAB-OH is a cathepsin cleavable ADC peptide linker for making MC-​Val-​Cit-​PAB, which is also known as MC-​Val-​Cit-​PAB-OH.
M13538 Z-WEHD-FMK Caspase
Z-WEHD-FMK is a potent, cell-permeable and irreversible caspase-1/5 inhibitor. Z-WEHD-FMK also exhibits a robust inhibitory effect on cathepsin B activity (IC50=6 μM). Z-WEHD-FMK can be used to investigate cells for evidence of apoptosis.
M20820 Gly-Phe β-naphthylamide Others
Gly-Phe beta-naphthylamide
Gly-Phe β-naphthylamide (Gly-Phe beta-naphthylamide) is a substrate of cathepsin C that accumulates within the lysosome. Gly-Phe-β-naphthylamide can inhibit the cathepsin-dependent activation of caspase-8.
M21400 LHVS Cathepsin
LHVS is a potent, non-selective, irreversible, cell-permeable inhibitor of cysteine protease and cathepsin. lHVS reduces actin ring formation. lHVS inhibits T. gondii invasion with an IC50 of 10 μM.
M27794 ALLM Proteasome
Calpain inhibitor II
ALLM (Calpain inhibitor II) is a potent inhibitor of calpain and cathepsin proteases. ALLM inhibits neuronal cell death and improves chronic neurological function after spinal cord injury (SCI).
M27825 KGP94  Cathepsin
KGP94 is a selective inhibitor of cathepsin L with an IC50 of 189 nM. KGP94 inhibits migration and invasion of metastatic carcinoma and shows low cytotoxicity (GI50=26.9 µM) against various human cell lines.
M28225 MIV-247  Cathepsin
MIV-247 is a selective cathepsin S inhibitor with Kis of 2.1, 4.2 and 7.5 nM for human, mouse and cynomolgus monkey cathepsin S, respectively.
M29515 K777  Cathepsin
K777 is a potent, orally active and irreversible cysteine protease inhibitor. K777 is also a potent CYP3A4 inhibitor with an IC50 of 60 nM and a selective CCR4 antagonist featuring the potent chemotaxis inhibition. K777 irreversibly inhibits Cruzain, the major cysteine protease of Trypansoma cruzi, and cathepsins B and L. K777 is a broad-spectrum antiviral by targeting cathepsin-mediated cell entry. K777 inhibits SARS-CoV and EBOV pseudovirus entry with IC50 values of 0.68 nM and 0.87 nM, respectively.
M29991 Relacatib Cathepsin
SB-462795
Relacatib (SB-462795) is a novel, potent, and orally active inhibitor of human cathepsins K, L, and V with Ki values of 41 pM, 68 pM, and 53 pM, respectively. Relacatib inhibits endogenous cathepsin K in situ in human osteoclasts and human osteoclast-mediated bone resorption with IC50 values of 45 nM and 70 nM, respectively. Relacatib inhibits bone resorption in vitro in human tissue as well as in cynomolgus monkeys in vivo.
M30755 ONO-5334  Cathepsin
ONO-5334 is a potent, selective and orally active cathepsin K inhibitor with Ki values of 0.10 nM, 0.049 nM and 0.85 nM for human, rabbit and rat cathepsin K, respectively. ONO 5334 is an effective antiviral compound against SAR-COV-2 virus activity with an EC50 value of 500 nM. ONO-5334 has the potential for the study of osteoporosis and COVID-19 disease.
M41002 AcLys-PABC-VC-Aur0101 intermediate-1 ADC Linker
AcLys-PABC-VC-Aur0101 intermediate-1 is a cathepsin cleavable ADC linker that is used for making antibody-drug conjugate.
M42922 Z-Nle-Lys-Arg-AMC Others
Z-Nle-Lys-Arg-AMC is a fluorogenic peptide substrate that specifically monitors cathepsin B activity over a broad pH range.
M43194 Cathepsin B Enzymes & Coenzymes
Cathepsin B is a cysteine protease and is involved in multiple kinds of programmed cell death (including apoptosis, pyroptosis, ferroptosis, necroptosis, and autophagic cell death).
M43254 Abz-HPGGPQ-EDDnp Others
Abz-HPGGPQ-EDDnp (Cathepsin K substrate) is a biological active peptide.
M43261 Ac-KQKLR-AMC Others
Ac-KQKLR-AMC (Cathepsin S substrate) is a biological active peptide.
M50354 Cathepsin L Enzymes & Coenzymes
Cathepsin L is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
M50355 Cathepsin K Enzymes & Coenzymes
Cathepsin K is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
M50356 Cathepsin D Enzymes & Coenzymes
Cathepsin D (CTSD) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
M50357 Cathepsin C Enzymes & Coenzymes
Cathepsin C is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
M50869 Abz-GIVRAK(Dnp) Others
Abz-GIVRAK(Dnp) is the most efficient substrate for cathepsin B and is highly selective for this enzyme among lysosomal cysteine proteases.
M51719 MeOSuc-AAPM-PNA Others
Cathepsin G substrate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
M52661 Suc-Val-Pro-Phe-pNA Cathepsin
Suc-Val-Pro-Phe-pNA is a substrate for cathepsin G and can be used to detect the activity of this enzyme.
M52668 Cathepsin D and E FRET Substrate Cathepsin
Cathepsin D and E FRET Substrate is a fluorogenic substrate for cathepsins D and E and not for B, H or L.
M52670 H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH Cathepsin
H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH is a water-soluble polypeptide that can serve as a substrate for cathepsin D, pepsin and pepsinogen.



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