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
Compound with spectra: 1 NMR
![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](/api/compound/9wR7yaos5zH.png?ph=true&h=300&w=458 "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")
| SpectraBase Compound ID | 9wR7yaos5zH |
|---|---|
| InChI | InChI=1S/C17H26N4O4S/c1-9-16(24)21-8-11(7-13(21)14(22)18-3)26-10(2)17(25)20-6-4-5-12(20)15(23)19-9/h9-13H,4-8H2,1-3H3,(H,18,22)(H,19,23)/t9-,10+,11?,12-,13?/m0/s1 |
| InChIKey | FZBKINQEKUKRQZ-SZQBSXBZSA-N |
| Mol Weight | 382.48 g/mol |
| Molecular Formula | C17H26N4O4S |
| Exact Mass | 382.167477 g/mol |
| Enantiomer InChIKey | FZBKINQEKUKRQZ-IJLVLRJLSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(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
METHYL-(2S.4S)-N-[(2R)-N-[(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL]-ALANYL]-4-(ACETYLTHIO)-PROLINATE
(2S,4S)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-(ACETYLTHIO)-PROLINE-METHYLAMIDE
N-TERT.-BUTYLOXYCARBONYLGLYCYL-S-PALMITOYL-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER
DRYMARIN_B
N-(6-MALEIMIDOCAPROYL)-GLYCYL-S-TERT.-BUTYLTHIO-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER
GYPSIN_B;CYCLO-(-LEU-(1)-PRO-(2)-TYR-(3)-PHEN-(4)-PRO(5)-GLY-(6))
Cyclo[(2S)-Amino-10-chloro-8(S),9(R)-isopropylideneswcanoyl)dimethylglycyl(S)-phenylalanyl(R)-prolyl]
EURYJANICIN_D;CYCLO-(-PHE-SER-PRO-ILE-PHE-PRO-ILE-)
GLYCYL-S-PALMITOYL-L-CYSTEYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER-HYDROTRIFLUOROACETATE
| 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 |