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#13;((S)-2-[(S)-2-[(S)-2-((S)-2-TERT.-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-PROPIONYLAMINO]-3-METHYL-BUTYRYLAMINO)-4-METHYL-PENTANOIC-ACID-METHYLESTER

Compound with spectra: 1 NMR

#13;((S)-2-[(S)-2-[(S)-2-((S)-2-TERT.-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-PROPIONYLAMINO]-3-METHYL-BUTYRYLAMINO)-4-METHYL-PENTANOIC-ACID-METHYLESTER
SpectraBase Compound ID ERL3rrPeRrq
InChI InChI=1S/C29H46N4O7/c1-17(2)15-22(27(37)39-9)31-26(36)23(18(3)4)33-24(34)19(5)30-25(35)21(16-20-13-11-10-12-14-20)32-28(38)40-29(6,7)8/h10-14,17-19,21-23H,15-16H2,1-9H3,(H,30,35)(H,31,36)(H,32,38)(H,33,34)/t19-,21+,22-,23-/m1/s1
InChIKey DFQSJTVEWKPIFE-CWKRKGSWSA-N
Mol Weight 562.7 g/mol
Molecular Formula C29H46N4O7
Exact Mass 562.33665 g/mol
Enantiomer InChIKey DFQSJTVEWKPIFE-MALNDZBISA-N

View Spectrum of #13;((S)-2-[(S)-2-[(S)-2-((S)-2-TERT.-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-PROPIONYLAMINO]-3-METHYL-BUTYRYLAMINO)-4-METHYL-PENTANOIC-ACID-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
L-Leucine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-leucyl]-L-isoleucyl]-, methyl ester
BOC-PHE-CYS((O)ME)-ALA-OALL
N-(N-((1,1-DIMETHYL)-ETHOXYCARBONYL)-L-PHENYLALANYL)-L-2-METHYLHISTIDINE-METHYLESTER,N-(N-((1,1-DIMETHYL)-ETHOXYCARBONYL)-L-PHENYLALANYL)-D-2
N-2-(TRIPHENYLSILYL)-ETHOXYCARBONYL-L-PHENYLALANYL-L-LEUCINE-TERT.-BUTYLESTER
SEGETALIN-G
(2S-(R*,R*))-N-(2-(((1,1-DIMETHYL)-ETHOXYCARBONYL)-AMINO)-1-OX-3-(3-THIENYL)-PROPYL)-HISTIDINE_METHYLESTER
2-[[2-[[2-[[2-amino-3-(4-hydroxyphenyl)propanoyl]amino]-4-hydroxy-4-keto-butanoyl]amino]-3-phenyl-propanoyl]amino]-4-methyl-valeric acid
L-Tyrosine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-L-leucyl]-, methyl ester
PAECILODEPSIPEPTIDE_B
ZRXWFXBQMNBHLR-PGGHDBDGSA-N
Title Journal or Book Year
Synthesis and Peptide Binding Properties of Methoxypyrrole Amino Acids (MOPAS) Organic Letters 2004
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