(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL
Compound with spectra: 1 NMR
![(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL](/api/compound/Ajv2rVTvY6W.png?ph=true&h=300&w=458 "(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL")
| SpectraBase Compound ID | Ajv2rVTvY6W |
|---|---|
| InChI | InChI=1S/C30H45N5O11S/c1-17(2)23(27(41)44-14-21(26(39)40)34-28(42)45-13-20-11-9-8-10-12-20)35-25(38)22(15-47-16-31-19(4)36)33-24(37)18(3)32-29(43)46-30(5,6)7/h8-12,17-18,21-23H,13-16H2,1-7H3,(H,31,36)(H,32,43)(H,33,37)(H,34,42)(H,35,38)(H,39,40)/t18-,21+,22-,23-/m0/s1 |
| InChIKey | WRUABNKUOUZZQB-AWDZXFJFSA-N |
| Mol Weight | 683.8 g/mol |
| Molecular Formula | C30H45N5O11S |
| Exact Mass | 683.283628 g/mol |
| Enantiomer InChIKey | WRUABNKUOUZZQB-YJSIEXFISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL
N-TERT.-BUTYLOXYCARBONYL-L-THREONYL-S-BENZYL-CYSTEINYL-ISOLEUCINE-METHYLESTER
ZAGASXZMQFWTCC-SFNPZSGNSA-N
BOC-PHE-CYS((O)ME)-SER(TERT.-BUTYL)-O(TERT.-BUTYL)
L-Leucine, N-[O-(1,1-dimethylethyl)-N-[N-[(phenylmethoxy)carbonyl]-L-.alpha.-glutamyl]-L-seryl]-, 5-(1,1-dimethylethyl) 1-methyl ester
N-(ALPHA)-(TERT.-BUTOXYCARBONYL)-O-(TERT.-BUTYL)-GLUTAMYL-O-(BENZYL)-SERYLLEUCINE-TERT.-BUTYLESTER
N-MYRISTOYL-GLYCYL-(S-PALMITOYL)-L-CYSTEYL-L-THREONYL-L-LEUCINE-ALLYLESTER;MYR-GLY-CYS(PAL)-THR-LEU-OALL
BOC-LEU-SER(BZL)-SER(BZL)-SER(BZL)-GLU(OBZL)-GLU(OBZL)-NHME
4-BENZYL-L-ASPARTYL-5-BENZYL-L-GLUTAMYL-O-BENZYL-L-THREONINE-METHYLESTER
BEAUVERIOLIDE-IV
| Title | Journal or Book | Year |
|---|---|---|
| Solution-Phase Synthesis of Nucleobase-Substituted Analogues of Triostin A | The Journal of Organic Chemistry | 2004 |