#11A;(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLORO
Compound with spectra: 1 NMR
![#11A;(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLORO](/api/compound/4NEHl9KaoqB.png?ph=true&h=300&w=458 "#11A;(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLORO")
| SpectraBase Compound ID | 4NEHl9KaoqB |
|---|---|
| InChI | InChI=1S/C57H81Cl3N10O19S2/c1-31(2)43(69-49(77)42(27-91-30-62-36(8)72)66-46(74)34(6)64-55(83)89-56(9,10)11)51(79)84-24-39(67-53(81)86-22-37-18-14-12-15-19-37)47(75)63-33(5)45(73)65-41(26-90-29-61-35(7)71)48(76)70-44(32(3)4)52(80)85-25-40(50(78)88-28-57(58,59)60)68-54(82)87-23-38-20-16-13-17-21-38/h12-21,31-34,39-44H,22-30H2,1-11H3,(H,61,71)(H,62,72)(H,63,75)(H,64,83)(H,65,73)(H,66,74)(H,67,81)(H,68,82)(H,69,77)(H,70,76)/t33-,34+,39+,40+,41-,42+,43+,44-/m0/s1 |
| InChIKey | LWOPEXMTSQFEEC-FYZZZALPSA-N |
| Mol Weight | 1380.8 g/mol |
| Molecular Formula | C57H81Cl3N10O19S2 |
| Exact Mass | 1378.418646 g/mol |
| Enantiomer InChIKey | LWOPEXMTSQFEEC-KIAWLJJESA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-(N-BUTYLOXYCARBONYL-L-VALINE)-O-TRICHLOROETHYL
CYCLO-[BETA-D-DAP-(THYMIN-1-YLACETYL)-L-ALA-L-CYS-L-VAL-BETA-D-DAP-(THYMIN-1-YLACETYL)-L-ALA-L-CYS-L-VAL]-DISULFIDE
SCOPULARIDE_A;CYCLO-(3-HYDROXY-4-METHYLDECANOYL-GLY-L-VYL-D-LEU-L-ALA-L-PHE)
BOC-SER-(PO3PH2)-LEU-SER-(PO3PH2)-SER-(PO3PH2)-SER-(PO3PH2)-GLU-(OBZL)-GLU-(OBZL)-NHME
ARENAMIDE_B
SCOPULARIDE_B;CYCLO-(3-HYDROXY-4-METHYLOCTANOYL-GLY-L-VYL-D-LEU-L-ALA-L-PHE)
SUSUITKPVHIIAO-JCDVXJHMSA-N
N-ALPHA-(TERT.-BUTOXYCARBONYL)-O-(BENZYL)-GLUTAMYL-O-DI-(4-BROMOBENZYL)-PHOSPHONOSERYLLEUCINE-BENZYLESTER;BOC-GLU(OBZL)-SER(PO3BRBZL2)-LEU-OBZL
CHBA-(NO2)NLE-PHE-VAL-OME
TERT.-BUTOXYCARBONYL-L-SERYL-L-TRYPTOPHYLGLYCINE-ETHYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Solution-Phase Synthesis of Nucleobase-Substituted Analogues of Triostin A | The Journal of Organic Chemistry | 2004 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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