D-ALA-SER-THR-THR-ASN-TYR-THR-NH2
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 25bKl0HWjmC |
|---|---|
| InChI | InChI=1S/C35H56N10O15/c1-13(36)29(54)41-22(12-46)32(57)43-26(16(4)49)34(59)45-27(17(5)50)35(60)44-25(15(3)48)33(58)40-21(11-23(37)52)30(55)39-20(10-18-6-8-19(51)9-7-18)31(56)42-24(14(2)47)28(38)53/h6-9,13-17,20-22,24-27,46-51H,10-12,36H2,1-5H3,(H2,37,52)(H2,38,53)(H,39,55)(H,40,58)(H,41,54)(H,42,56)(H,43,57)(H,44,60)(H,45,59)/t13-,14+,15+,16+,17+,20-,21+,22+,24-,25+,26+,27+/m1/s1 |
| InChIKey | AKWRNBWMGFUAMF-BPPVZSLBSA-N |
| Mol Weight | 856.9 g/mol |
| Molecular Formula | C35H56N10O15 |
| Exact Mass | 856.392661 g/mol |
| Enantiomer InChIKey | AKWRNBWMGFUAMF-ZQAFMGFBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6:D2O=1:9 |
DELAVAYIN-A;CYClO-(-GLY-SER-GAMMA-HYDROXY-ILE-PHE-PHE-ALA-)
2-[[2-[[2-[[2-[[2-[[2-[[2-[(2-amino-5-hydroxy-5-keto-pentanoyl)amino]-3-(4-hydroxyphenyl)propanoyl]amino]-5-hydroxy-5-keto-pentanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-methyl-pentanoyl]amino]-4-hydroxy-4-keto-butanoyl]amino]-3-(4-hydroxyphenyl)p
CROTOGOSSAIDE;CYCLO-(-GLY-(1)-ALA-(2)-SER-(3)-GLY-(4)-LEU-(5)-ASN-(6)-GLY-(7)-ILE-(8)-PHE-(9)-)
N-TERT.-BUTYLOXYCARBONYL-GLYCYL-(S-PALMITOYL)-L-CYSTEYL-L-THREONYL-L-LEUCYL-L-SERYL-L-ALANINE;BOC-GLY-CYS(PAL)-THR-LEU-SER-ALA-OH
TEOC-(3-NCP)ALA-PHE-VAL-OME
TMC-89-A
L-Glutamic acid, N-[N-[N-[S-(2-methoxy-2-oxoethyl)-N-(trifluoroacetyl)-L-cysteinyl]-O-methyl-L-tyrosyl]-L-phenylalanyl]-, dimethyl ester
BEAUVERIOLIDE-VII
SOLONAMIDE-B
SOLONAMIDE-A
| Title | Journal or Book | Year |
|---|---|---|
| Protected-mode synthesis of N-linked glycopeptides: single-step preparation of building blocks as peracetyl glycosylated NαFmoc asparagine OPfp esters | J. Chem. Soc., Perkin Trans. 1 | 1993 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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