(1S,3R,9S,12R,15S)-3,12-DIMETHYL-4,10,13-TRIOXO-2-THIA-5,11,14-TRIAZATRICYCLO-[12.2.1.0(5,9)]-HEPTADECANE-15-CARBOXYLIC-ACID
Compound with spectra: 1 NMR
![(1S,3R,9S,12R,15S)-3,12-DIMETHYL-4,10,13-TRIOXO-2-THIA-5,11,14-TRIAZATRICYCLO-[12.2.1.0(5,9)]-HEPTADECANE-15-CARBOXYLIC-ACID](/api/compound/6csKg6k4hDI.png?ph=true&h=300&w=458 "(1S,3R,9S,12R,15S)-3,12-DIMETHYL-4,10,13-TRIOXO-2-THIA-5,11,14-TRIAZATRICYCLO-[12.2.1.0(5,9)]-HEPTADECANE-15-CARBOXYLIC-ACID")
| SpectraBase Compound ID | 6csKg6k4hDI |
|---|---|
| InChI | InChI=1S/C16H23N3O5S/c1-8-14(21)19-7-10(6-12(19)16(23)24)25-9(2)15(22)18-5-3-4-11(18)13(20)17-8/h8-12H,3-7H2,1-2H3,(H,17,20)(H,23,24)/t8-,9+,10?,11-,12?/m0/s1 |
| InChIKey | YFMFWXBTYAOOTI-UXGOBAPMSA-N |
| Mol Weight | 369.44 g/mol |
| Molecular Formula | C16H23N3O5S |
| Exact Mass | 369.135842 g/mol |
| Enantiomer InChIKey | YFMFWXBTYAOOTI-TZMBILIQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-METHYL-[(1S,3R,9S,12R,15S)-3,12-DIMETHYL-4,10,13-TRIOXO-2-THIA-5,11,14-TRIAZATRICYCLO-[12.2.1.0(5,9)]-HEPTADECANE]-15-CARBOXAMIDE
N-[(1S,3R,9S,12R,15S)-3,12-DIMETHYL-4,10,13-TRIOXO-2-THIA-5,11,14-TRIAZATRICYCLO-[12.2.1.0(5,9)]-HEPTADECAN-15-YLCARBONYL]-N,N'-(DIMETHYL)-ETHYLEN
N-(6-MALEIMIDOCAPROYL)-GLYCYL-S-TERT.-BUTYLTHIO-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-FARNESYL-L-CYSTEINE-METHYLESTER
N-TERT.-BUTYLOXYCARBONYLGLYCYL-S-PALMITOYL-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER
DELAVAYIN-C;CYClO-(-GLY-TYR-TYR-TYR-PRO-VAL-PRO-)
N-(6-MALEIMIDOCAPROYL)-GLYCYL-S-TERT.-BUTYLTHIO-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER
CYCLOMONTANIN-D;CYCLO-(-ASPARAGINYL-PROLYL-GLYCYL-LEUCYL-PROLYL-TYROSINYL-ALANYL-)
N-(6-MALEIMIDOCAPROYL)-GLYCYL-S-PALMITOYL-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-L-SERINE-METHYLESTER
GLYCYL-S-PALMITOYL-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER-HYDROTRIFLUOROACETATE
TERT.-BUTYLOXYCARBONYL-L-SERYL-L-LEUCYL-L-PROLYL-L-GLUTAMINYL-N(EPSILON)-BENZYLOXYCARBONYL-L-LYSINE-BENZYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Design, construction and properties of peptide N-terminal cap templates devised to initiate α-helices. Part 3.† Caps derived from N-[(2S )-2-chloropropionyl]-(2S )-Pro-(2R)-Ala-(2S,4S )-4-thioPro-OMe | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |