benzyl N-[(1S)-5-amino-1-benzylsulfanylcarbonyl-pentyl]carbamate
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![benzyl N-[(1S)-5-amino-1-benzylsulfanylcarbonyl-pentyl]carbamate structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220811/8b8683f4bd204f409c808371fa8e2dd1.png "benzyl N-[(1S)-5-amino-1-benzylsulfanylcarbonyl-pentyl]carbamate")
benzyl N-[(1S)-5-amino-1-benzylsulfanylcarbonyl-pentyl]carbamate
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CAS No:
69861-90-1
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Formula:
C21H26N2O3S
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Chemical Name:
benzyl N-[(1S)-5-amino-1-benzylsulfanylcarbonyl-pentyl]carbamate
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Synonyms:
alpha-N-carbobenzyloxy-L-lysine thiobenzyl ester;Cbz-lysine thiobenzyl ester;N-carbobenzyloxylysine thiobenzyl ester;thiobenzyl benzyloxycarbonyl-L-lysinate;BLT Esterase;Hexanethioic acid, 6-amino-2-(((phenylmethoxy)carbonyl)amino)-, S-(phenylmethyl) ester, (S)-;Hexanethioic acid, 6-amino-2-[[(phenylmethoxy)carbonyl]amino]-, S-(phenylmethyl) ester, (S)-
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CAS No:
Description
Thiobenzyl benzyloxycarbonyl-L-lysinate is an L-lysine derivative that is L-lysine in which the amino group is replaced by a [(benzyloxy)carbonyl]amino group and the carboxy group is replaced by a (benzylsulfanyl)carbonyl group. It is a substrate for a sensitive colorimetric assay for trypsin-like enzymes. It is a L-lysine derivative, a thiocarboxylic ester, a primary amino compound, a benzyl ester and a carbamate ester. It is a conjugate base of a thiobenzyl benzyloxycarbonyl-L-lysinate(1+).
benzyl N-[(1S)-5-amino-1-benzylsulfanylcarbonyl-pentyl]carbamate Basic Attributes
386.51
386.166
DTXSID90220154
Computed Properties
Molecular Weight:386.5
XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:12
Exact Mass:386.16641387
Monoisotopic Mass:386.16641387
Topological Polar Surface Area:107
Heavy Atom Count:27
Complexity:435
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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