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| | Boc-Arg-Val-Arg-Arg-AMC Basic information |
| Product Name: | Boc-Arg-Val-Arg-Arg-AMC | | Synonyms: | BOC-RVRR-AMC;BOC-ARG-VAL-ARG-ARG-7-AMIDO-4-METHYLCOUMARIN;N-T-boc-arg-val-arg-arg 7-amido-4-*methylcoumarin;N-BOC-Arg-Val-Arg-Arg-7-amido-4-methylcoumarin acetate;Boc-Arg-Val-Arg-Arg-7-amido-4-methylcoumarin acetate salt;L-Argininamide,N2-[(1,1-dimethylethoxy)carbonyl]-L-arginyl-L-valyl-L-arginyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-,monohydrochloride;Boc-Arg-Val-Arg-Arg-AMC(hydrochloride);Boc-Arg-Val-Arg-Arg-AMC | | CAS: | 136132-77-9 | | MF: | C38H62N14O8 | | MW: | 842.99 | | EINECS: | | | Product Categories: | | | Mol File: | 136132-77-9.mol |  |
| | Boc-Arg-Val-Arg-Arg-AMC Chemical Properties |
| storage temp. | -20°C | | form | White to off-white powder. | | color | White to off-white | | Sequence | {Boc-Arg}-Val-Arg-{Arg-AMC} |
| | Boc-Arg-Val-Arg-Arg-AMC Usage And Synthesis |
| Uses | Boc-Arg-Val-Arg-Arg-AMC hydrochloride (Boc-RVRR-AMC) is a synthetic fluorogenic substrate that is efficiently cleaved by furin[1]. | | References | [1] Wanyiri JW, et al. Proteolytic processing of the Cryptosporidium glycoprotein gp40/15 by human furin and by a parasite-derived furin-like protease activity. Infect Immun. 2007 Jan;75(1):184-92. DOI:10.1128/IAI.00944-06 |
| | Boc-Arg-Val-Arg-Arg-AMC Preparation Products And Raw materials |
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