Others - BioCrick

Cat.No. Product Name Information/Activity

BCC1126 Z-VAD-FMK Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan-caspase inhibitor. Z-VAD(OMe)-FMK is an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor. Z-VAD(OMe)-FMK irreversibly modifies UCHL1 by targeting the active site of UCHL1. Z-VAD-FMK chemical structure

BCC3944 A 205804 A-205804 is an orally bioavailable, potent and selective lead inhibitor of E-selectin and ICAM-1 expression, with an IC50 of 20 nM and 25 nM for E-selectin and ICAM-1, respectively. A-205804 can be used in the research of chronic inflammatory diseases. A 205804 chemical structure

BCC3946 A 286982 Potent inhibitor of the LFA-1/ICAM-1 interaction A 286982 chemical structure

BCC3945 BIO 1211 Selective α4β1 (VLA-4) inhibitor BIO 1211 chemical structure

BCC8002 BIO 5192 327613-57-0 BIO 5192 chemical structure

BCC3942 Cilengitide Cilengitide, a cyclic RGD-containing peptide, is a potent and selective integrin inhibitor for αvβ3 and αvβ5 receptor, with IC50s of 4 and 79 nM, respectively. Cilengitide chemical structure

BCC5988 Echistatin, α1 isoform 154303-05-6 Echistatin, α1 isoform chemical structure

BCC6998 GR 144053 trihydrochloride 1215333-48-4 GR 144053 trihydrochloride chemical structure

BCC3943 MNS MNS is a potent and selective inhibitor of Src and Syk tyrosine kinases. MNS chemical structure

BCC6275 P11 848644-86-0 P11 chemical structure

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