(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL
Compound with spectra: 1 NMR
![(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL](/api/compound/FFHFitq1fOQ.png?ph=true&h=300&w=458 "(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL")
| SpectraBase Compound ID | FFHFitq1fOQ |
|---|---|
| InChI | InChI=1S/C32H46Cl3N5O11S/c1-18(2)24(40-26(43)23(15-52-17-36-20(4)41)38-25(42)19(3)37-30(47)51-31(5,6)7)28(45)48-14-22(27(44)50-16-32(33,34)35)39-29(46)49-13-21-11-9-8-10-12-21/h8-12,18-19,22-24H,13-17H2,1-7H3,(H,36,41)(H,37,47)(H,38,42)(H,39,46)(H,40,43)/t19-,22+,23-,24-/m0/s1 |
| InChIKey | XCCZUUKVTPMSJY-UQAQOTMJSA-N |
| Mol Weight | 815.2 g/mol |
| Molecular Formula | C32H46Cl3N5O11S |
| Exact Mass | 813.198012 g/mol |
| Enantiomer InChIKey | XCCZUUKVTPMSJY-OYYPCOLYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
TERT.-BUTOXYCARBONYL-L-ALANYL-GAMMA-BENZYL-L-GLUTAMYLGLYCYL-L-GLUTAMINYL-N-(EPSILON)-BENZOYLOXYCARBONYL-L-LYSINE-BENZYLESTER
BOC-PHE-CYS(ME)-CYS(TRT)-OME
N-TERT.-BUTYLOXYCARBONYL-GLYCYL-(S-PALMITOYL)-L-CYSTEYL-L-THREONYL-L-LEUCINE-CHOLINE-ESTER-BROMIDE;BOC-GLY-CYS(PAL)-THR-LEU-CHO
N-Benzyloxycarbonylglycyl-S-trityl-L-cysteinyl-L -phenylalanine benzyl ester
N-TERT.-BUTYLOXYCARBONYL-GLYCYL-(S-PALMITOYL)-L-CYSTEYL-L-THREONYL-L-LEUCYL-L-SERYL-L-ALANINE;BOC-GLY-CYS(PAL)-THR-LEU-SER-ALA-OH
BOC-GLU(O-BZL)-ABU(PO3ME2)-LEU-O-BZL;N-ALPHA-(TERT.-BUTYLOXYCARBONYL)-O-BENZYLGLUTAMYL-4-(DIMETHYLPHOSPHONO)-2-AMINOBUTANOYLLEUCINE-BENZYLESTER
BEAUVERIOLIDE-VII
CYCLIC_TRICHRYSOBACTIN
BEAUVERIOLIDE-VIII
BEAUVERIOLIDE-V
| Title | Journal or Book | Year |
|---|---|---|
| Solution-Phase Synthesis of Nucleobase-Substituted Analogues of Triostin A | The Journal of Organic Chemistry | 2004 |