Boc-Leu-Arg-Arg-AMC . 2 HCl

Boc-Leu-Arg-Arg-AMC · 2 HCl is a fluorogenic substrate combining a protected tripeptide with an AMC reporter. The basic residues direct recognition by specific proteases. Its Boc group improves handling during synthesis and storage. Research applications include kinetic assays, specificity profiling, and mechanistic enzymology.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Boc-Leu-Arg-Arg-AMC . 2 HCl(CAS 109358-46-5)

CAT No: P6306

CAS No:109358-46-5

Synonyms/Alias:109358-46-5;Boc-LRR-AMC;Boc-Leu-Arg-Arg-AMC;Boc-Leu-Arg-Arg-AMC . 2 HCl;Boc-Leu-Arg-Arg-AMC Dihydrochloride;N-[(1,1-dimethylethoxy)carbonyl]-L-leucyl-L-arginyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-argininamide;tert-butyl N-[(2S)-1-[[(2S)-5-(diaminomethylideneamino)-1-[[(2S)-5-(diaminomethylideneamino)-1-[(4-methyl-2-oxochromen-7-yl)amino]-1-oxopentan-2-yl]amino]-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]carbamate;Boc-LRR-AMC (trifluoroacetate salt);N-[(1,1-Dimethylethoxy)carbonyl]-L-leucyl-L-arginyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-argininamide Dihydrochloride;Boc-Leu-Arg-Arg-MCA;SCHEMBL2199089;AKOS040755573;FB110557;HY-115391;CS-0083184;Boc-Leu-Arg-Arg-AMC, Boc-Leu-Arg-Arg-7-amido-4-Methylcoumarin, Boc-LRR-AMC;tert-butyl N-[(1S)-1-{[(1S)-4-carbamimidamido-1-{[(1S)-4-carbamimidamido-1-[(4-methyl-2-oxochromen-7-yl)carbamoyl]butyl]carbamoyl}butyl]carbamoyl}-3-methylbutyl]carbamate;

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M.F/Formula
C33H52N10O7
M.W/Mr.
700.8
Sequence
One Letter Code:LRR
Three Letter Code:Boc-Leu-Arg-Arg-AMC
InChI
InChI=1S/C33H52N10O7/c1-18(2)15-24(43-32(48)50-33(4,5)6)29(47)42-23(10-8-14-39-31(36)37)28(46)41-22(9-7-13-38-30(34)35)27(45)40-20-11-12-21-19(3)16-26(44)49-25(21)17-20/h11-12,16-18,22-24H,7-10,13-15H2,1-6H3,(H,40,45)(H,41,46)(H,42,47)(H,43,48)(H4,34,35,38)(H4,36,37,39)/t22-,23-,24-/m0/s1
InChI Key
BAVWXCNIABBHLQ-HJOGWXRNSA-N

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