(2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTANOYL-L-LEUCYL-L-PROLYL-L-PROLINE;PROBESTIN
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 3fbCrZ1IvOd |
|---|---|
| InChI | InChI=1S/C26H38N4O6/c1-16(2)14-19(28-23(32)22(31)18(27)15-17-8-4-3-5-9-17)24(33)29-12-6-10-20(29)25(34)30-13-7-11-21(30)26(35)36/h3-5,8-9,16,18-22,31H,6-7,10-15,27H2,1-2H3,(H,28,32)(H,35,36)/t18-,19+,20+,21+,22+/m1/s1 |
| InChIKey | CEQMEILRVSCKGT-FXTUREPZSA-N |
| Mol Weight | 502.6 g/mol |
| Molecular Formula | C26H38N4O6 |
| Exact Mass | 502.279135 g/mol |
| Enantiomer InChIKey | CEQMEILRVSCKGT-ZSYZGHEHSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
MR-387B
Methyl (2S,4R)-N-[N-{(2S)-N-[(2S)-2-Chloropropionyl]prolyl}prolyl]-4-hydroxyprolinate
METHYL-(2S,4S)-N-((2S)-N-{(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL)-PROLYL}-4-HYDROXYPROLINATE
(2S,4S)-1-[(2S)-1-[(2S)-1-[(2S)-2-chloropropanoyl]prolyl]prolyl]-4-hydroxy-pyrrolidine-2-carboxylic acid methyl ester
(2S,4S)-N-[(2S)-N-[(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL]-PROLYL]-4-MERCAPTOPROLINE-METHYLAMIDE
(2R,3R/2S,3S)-N-[(3-CARBOXY-AZIRIDINE-2-YL)-CARBONYL]-(S)-LEUCYL-(S)-PROLINE-BENZYLESTER-TRIFLUOROACETATE
L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-[(E,E)-8-O-(2-N-METHYL-AMINOBENZOYL)-3,7-DIMETHYL-2,6-OCTANDIENE]-L-CYSTEINE-METHYLESTER
TERT.-BUTYLOXYCARBONYL-L-LEUCYL-L-PROLYL-L-GLUTAMINYL-N(EPSILON)-BENZYLOXYCARBONYL-L-LYSINE-BENZYLESTER
N-TERT.-BUTYLOXYCARBONYLGLYCYL-S-TERT.-BUTYLTHIO-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER
N-TERT.-BUTYLOXYCARBONYLGLYCYL-S-PALMITOYL-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-L-SERINE-METHYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Probestin, a new inhibitor of aminopeptidase M, produced by Streptomyces azureus MH663-2F6. II. Structure determination of probestin. | The Journal of Antibiotics | 1990 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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