N-METHYL-(R)-2-[(R)-2-(HYDROXYAMINO)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE
Compound with spectra: 1 NMR
![N-METHYL-(R)-2-[(R)-2-(HYDROXYAMINO)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE](/api/compound/9wYsmsEE7fJ.png?ph=true&h=300&w=458 "N-METHYL-(R)-2-[(R)-2-(HYDROXYAMINO)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE")
| SpectraBase Compound ID | 9wYsmsEE7fJ |
|---|---|
| InChI | InChI=1S/C28H38N4O6/c1-28(2,3)38-27(36)31-23(26(35)32-37)21(17-11-16-19-12-7-5-8-13-19)24(33)30-22(25(34)29-4)18-20-14-9-6-10-15-20/h5-10,12-15,21-23,37H,11,16-18H2,1-4H3,(H,29,34)(H,30,33)(H,31,36)(H,32,35)/t21-,22+,23-/m1/s1 |
| InChIKey | NDSWSBIHGOECPI-XPWALMASSA-N |
| Mol Weight | 526.6 g/mol |
| Molecular Formula | C28H38N4O6 |
| Exact Mass | 526.279135 g/mol |
| Enantiomer InChIKey | NDSWSBIHGOECPI-ZRBLBEILSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
N-METHYL-(R)-2-[(R)-2-(METHYLOXY)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE
BENZYL-[(2R)-N-(TERT.-BUTOXYCARBONYL)-ALPHA-METHYL-ASPARTYL]-BETA-(2S)-PHENYLALANYL-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSINATE-TRIESTER;COMPOUN
CROTOGOSSAIDE;CYCLO-(-GLY-(1)-ALA-(2)-SER-(3)-GLY-(4)-LEU-(5)-ASN-(6)-GLY-(7)-ILE-(8)-PHE-(9)-)
BEAUVERIOLIDE-VII
1962_B
SOLONAMIDE-B
BOC-PHE-CYS(ME)-CYS(TRT)-OME
TEOC-(3-NCP)ALA-PHE-VAL-OME
UNNARMICIN_A
L-Glutamic acid, N-[N-[N-[S-(2-methoxy-2-oxoethyl)-N-(trifluoroacetyl)-L-cysteinyl]-O-methyl-L-tyrosyl]-L-phenylalanyl]-, dimethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| A Straightforward Approach to MMP-2 and MMP-9 Inhibitors Based on Chelate Claisen Rearrangements | European Journal of Organic Chemistry | 2011 |