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BENZYL-N-(TERT.-BUTOXYCARBONYL)-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSINATE-DIESTER

Compound with spectra: 1 NMR, and 1 MS (GC)

BENZYL-N-(TERT.-BUTOXYCARBONYL)-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSINATE-DIESTER
SpectraBase Compound ID 1RboLTHAdHn
InChI InChI=1S/C24H35N3O8/c1-24(2,3)35-23(32)25-14-13-19(28)26-18(22(31)33-5)11-12-20(29)27(4)15-21(30)34-16-17-9-7-6-8-10-17/h6-10,18H,11-16H2,1-5H3,(H,25,32)(H,26,28)/t18-/m1/s1
InChIKey JNMYFCPRNQZIAV-GOSISDBHSA-N
Mol Weight 493.6 g/mol
Molecular Formula C24H35N3O8
Exact Mass 493.242415 g/mol
Enantiomer InChIKey JNMYFCPRNQZIAV-SFHVURJKSA-N
Racemate InChIKey JNMYFCPRNQZIAV-UHFFFAOYSA-N

View Spectrum of BENZYL-N-(TERT.-BUTOXYCARBONYL)-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSINATE-DIESTER

MS (GC) Spectrum
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Source of Spectrum KC-0-2506-25

View Spectrum of BENZYL-N-(TERT.-BUTOXYCARBONYL)-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSINATE-DIESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (2R)-5-[(2-benzoxy-2-keto-ethyl)-methyl-amino]-2-[3-(tert-butoxycarbonylamino)propanoylamino]-5-keto-valeric acid methyl ester
4-[(2-Allyloxycarbonylamino-ethyl)-methyl-carbamoyl]-2-decanoylamino-butyric acid benzyl ester
.beta.-Allyl (2R)-[.alpha.-methylglutamyl]-gamma.-sarcosyl-[.alpha.-methyl (2R)-aspartate] triester hydrochoride
METHYL-N-(BENZYLOXYCARBONYL)-BETA-ALANYLVALYLVALINE
Boc-Gln-Ala-Ala-OCH2Ph
L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-, 1-(phenylmethyl)ester, 5-[2-[4-(hydroxymethyl)phenyl]hydrazide]
BOC-LYS-(Z)-SER-OME
(3S,5R)-5-(N-Benzyloxycarbonylaminomethyl)-3-(tert-butoxycarbonylamino)-.delta.-butyrolactone
XFMIJAHBOMBWRO-UHFFFAOYSA-N
2-Azabicyclo[2.2.0]hex-5-ene-2-acetic acid, 3-oxo-, phenylmethyl ester
BENZYLOXYCARBONYL-VALINE-GLYCINE-(TERT-BUTYLOXYCARBONYL)LYSINETRIPEPTIDE
Title Journal or Book Year
Design and preparation of serine–threonine protein phosphatase inhibitors based upon the nodularin and microcystin toxin structures: Part 1. Evaluation of key inhibitory features and synthesis of a rationally stripped-down nodularin macrocycle Journal of the Chemical Society, Perkin Transactions 1 1997
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