BETA-BENZYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSYL-[ALPHA-METHYL-(2R)-ASPARTATE]-TRIESTER-HYDROCHLORIDE;ROTAMER-#2
Compound with spectra: 1 NMR
![BETA-BENZYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSYL-[ALPHA-METHYL-(2R)-ASPARTATE]-TRIESTER-HYDROCHLORIDE;ROTAMER-#2](/api/compound/LJQch5GRIeF.png?ph=true&h=300&w=458 "BETA-BENZYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSYL-[ALPHA-METHYL-(2R)-ASPARTATE]-TRIESTER-HYDROCHLORIDE;ROTAMER-#2")
| SpectraBase Compound ID | LJQch5GRIeF |
|---|---|
| InChI | InChI=1S/C21H29N3O8.ClH/c1-24(18(26)10-9-15(22)20(28)30-2)12-17(25)23-16(21(29)31-3)11-19(27)32-13-14-7-5-4-6-8-14;/h4-8,15-16H,9-13,22H2,1-3H3,(H,23,25);1H/t15-,16+;/m0./s1 |
| InChIKey | UDIXYGVUVYWBTQ-IDVLALEDSA-N |
| Mol Weight | 487.94 g/mol |
| Molecular Formula | C21H30ClN3O8 |
| Exact Mass | 487.172143 g/mol |
| Parent InChIKey | AREADXHQVSAQQA-JKSUJKDBSA-N |
| Enantiomer InChIKey | UDIXYGVUVYWBTQ-RCPFAERMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
N-[(-)-jasmonoyl]-(S)-aspartic acid dimethylesther
N-(N-CARBOXY-L-gamma-GLUTAMYL)-L-GLUTAMIC ACID, N,alpha,1-TRIBENZYL ESTER
L-Alanine, N-(1-acetyl-L-prolyl)-, phenylmethyl ester
TERT.-BUTOXYCARBONYL-L-ALANYL-GAMMA-BENZYL-L-GLUTAMYL-GLYCINE
METHYL-N-(BENZYLOXYCARBONYL)-GLYCYLMETHIONYLMETHIONINE
METHYL-N-(BENZYLOXYCARBONYL)-BETA-ALANYLLEUCYLLEUCINE
METHYL-N-(BENZYLOXYCARBONYL)-GLYCYLLEUCYLLEUCINE
L-Glutamic acid, N-(N-decanoyl-L-.alpha.-glutamyl)-, trimethyl ester
butanoic acid, 4-[(1-carboxy-2-hydroxyethyl)amino]-4-oxo-3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Design and preparation of serine–threonine protein phosphatase inhibitors based upon the nodularin and microcystin toxin structures: Part 1. Evaluation of key inhibitory features and synthesis of a rationally stripped-down nodularin macrocycle | Journal of the Chemical Society, Perkin Transactions 1 | 1997 |