N-METHYL-(R)-2-[(R)-2-(BENZYLOXYAMINO)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE
Compound with spectra: 1 NMR
![N-METHYL-(R)-2-[(R)-2-(BENZYLOXYAMINO)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE](/api/compound/IAYafLjdPKX.png?ph=true&h=300&w=458 "N-METHYL-(R)-2-[(R)-2-(BENZYLOXYAMINO)-1-(TERT.-BUTOXYCARBONYLAMINO)-2-OXO-ETHYL]-5-PHENYLPENTANOYL-(S)-PHENYLALANINEAMIDE")
| SpectraBase Compound ID | IAYafLjdPKX |
|---|---|
| InChI | InChI=1S/C35H44N4O6/c1-35(2,3)45-34(43)38-30(33(42)39-44-24-27-19-12-7-13-20-27)28(22-14-21-25-15-8-5-9-16-25)31(40)37-29(32(41)36-4)23-26-17-10-6-11-18-26/h5-13,15-20,28-30H,14,21-24H2,1-4H3,(H,36,41)(H,37,40)(H,38,43)(H,39,42)/t28-,29+,30-/m1/s1 |
| InChIKey | KULPNDLCXGASDY-DYIKCSJPSA-N |
| Mol Weight | 616.8 g/mol |
| Molecular Formula | C35H44N4O6 |
| Exact Mass | 616.326085 g/mol |
| Enantiomer InChIKey | KULPNDLCXGASDY-JBOQNHBVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
TYR-(1-S,2-R)-ACHC-PHE-PARA-F-PHE-NH2
(2S,3R)-3-ENDO-[1-(1-METHOXYCARBONYL-ETHYLCARBAMOYL)-2-PHENYL-ETHYLCARBAMOYL]-BICYCLO-[2.2.1]-HEPTANE-2-ENDO-CARBOXYLIC-ACID
1H-indole-3-propanamide, alpha-[[(4-methylcyclohexyl)carbonyl]amino]-N-(6-methyl-2-pyridinyl)-
CITRUSIN-I
Polymyxin B sulfate salt
SCOPULARIDE_A;CYCLO-(3-HYDROXY-4-METHYLDECANOYL-GLY-L-VYL-D-LEU-L-ALA-L-PHE)
CHPCA-(NO2)NLE-PHE-VAL-OME
BEAUVERIOLIDE-3;CYCLO-[(3-S,4-S)-3-HYDROXY-4-METHYL-OCTANOYL-L-PHENYL-ALANYL-L-ALANYL-D-ALLO-ISOLEUCYL]
ARENAMIDE_B
BEAUVEROLIDE-LA;CYCLO-[3-HYDROXY-4-METHYLDECANOYL-L-PHENYL-ALANYL-D-ALLO-ISOLEUCYL]
| 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 |