N-METHYL-(R)-2-[(R)-2-(HYDROXYAMINO)-1-(BENZOYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE
Compound with spectra: 1 NMR
![N-METHYL-(R)-2-[(R)-2-(HYDROXYAMINO)-1-(BENZOYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE](/api/compound/2WA6mMdzAMp.png?ph=true&h=300&w=458 "N-METHYL-(R)-2-[(R)-2-(HYDROXYAMINO)-1-(BENZOYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE")
| SpectraBase Compound ID | 2WA6mMdzAMp |
|---|---|
| InChI | InChI=1S/C30H34N4O5/c1-31-29(37)25(20-22-14-7-3-8-15-22)32-28(36)24(19-11-16-21-12-5-2-6-13-21)26(30(38)34-39)33-27(35)23-17-9-4-10-18-23/h2-10,12-15,17-18,24-26,39H,11,16,19-20H2,1H3,(H,31,37)(H,32,36)(H,33,35)(H,34,38)/t24-,25+,26-/m1/s1 |
| InChIKey | HGCZPMIQBNZROL-UODIDJSMSA-N |
| Mol Weight | 530.6 g/mol |
| Molecular Formula | C30H34N4O5 |
| Exact Mass | 530.25292 g/mol |
| Enantiomer InChIKey | HGCZPMIQBNZROL-NXCFDTQHSA-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-(BENZYLOXYAMINO)-1-(2-HYDROXYACETYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE
TYR-(1-S,2-R)-ACHC-PHE-PARA-F-PHE-NH2
N-(N-benzoyl-(O-benzyl-L-threonyl)-L-alanyl-L-phenylalanyl)-L-homoserine lactone
CHPCA-(NO2)NVA-PHE-VAL-OME
(2S,3R)-[2-({3-endo-[1-(Benzyloxycrbonylmethylcarbamoyl)-2-phenylethylcarbomoyl]bicyclo[2.2.1]heptane-2-endo-carbonyl}amino)-3-phenylpropionylamino]propionic acid methyl ester
(2S,3R)-3-endo-[1-(1-Methoxycrbonylethylcarbamoyl)-2-phenylethylcarbomoyl]bicyclo[2.2.1]heptane-2-endo-carboxylic acid
KAHALALIDE_X
BEAUVERIOLIDE-3;CYCLO-[(3-S,4-S)-3-HYDROXY-4-METHYL-OCTANOYL-L-PHENYL-ALANYL-L-ALANYL-D-ALLO-ISOLEUCYL]
BEAUVEROLIDE-LA;CYCLO-[3-HYDROXY-4-METHYLDECANOYL-L-PHENYL-ALANYL-D-ALLO-ISOLEUCYL]
CHPCA-PHE-PHE-VAL-OME
| 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 |