(2S)-N2-(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)-PHENYLALANINE-METH
Compound with spectra: 1 NMR
![(2S)-N2-(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)-PHENYLALANINE-METH](/api/compound/9RuZdvb8xo8.png?ph=true&h=300&w=458 "(2S)-N2-(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)-PHENYLALANINE-METH")
| SpectraBase Compound ID | 9RuZdvb8xo8 |
|---|---|
| InChI | InChI=1S/C26H35N5O5S/c1-15-25(35)31-14-18(37-16(2)26(36)30-11-7-10-20(30)23(33)28-15)13-21(31)24(34)29-19(22(32)27-3)12-17-8-5-4-6-9-17/h4-6,8-9,15-16,18-21H,7,10-14H2,1-3H3,(H,27,32)(H,28,33)(H,29,34)/t15-,16+,18?,19+,20-,21?/m0/s1 |
| InChIKey | TXEGCINHEHLLDP-VKQJHHAPSA-N |
| Mol Weight | 529.7 g/mol |
| Molecular Formula | C26H35N5O5S |
| Exact Mass | 529.23589 g/mol |
| Enantiomer InChIKey | TXEGCINHEHLLDP-UYZJDOOPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2S)-N2-[(2S)-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]-ALANYL]-P
(3S,9S,15R,17S,19S,22S,28S,34R,36S,38S)-15,34-DIMETHYL-2,8,14,21,27,33-HEXAOXO-16,35-DITHIA-1,7,13,20,26,32-HEXAAZAHEPTACYCLO-[34.2.1.1^17,20.0^3,
GYPSIN_C;CYCLO-(-ALA(1)-PRO-(2)-TYR-(3)-LEU-(4)-LEU-(5)-PRO-(6)-PRO-(7)-ALA-(8))
CYCLOLEONURIPEPTIDE_E;CYCLO-(-ALA-PRO-ILE-VAL-ALA-ALA-PHE-THR-PRO-)
L-(-)-N^2-{N-{1-{N-{N-{N-[1-(1-L-ARGINYL-L-PROLYL)-L-PROLYL]GLYCYL}-3-PHENYL-L-ALANYL}GLYCYL}-L-PROLYL}-3-PHENYL-L-ALANYL}ARGININE, DIACETATE, PENTAHYDRATE
(2-Phenylalanine-4-leucine)-ocytocin
LOLOATIN-A;CYClIC-(L-ASPARAGINYL-L-ASPARTYL-L-TYROSYL-L-VALYL-L-ORNITHINYL-L-LEUCYL-D-TYROSYL-L-PROLYL-L-PHENYLALANYL-D-PHENYLALANYL)
STYLOPEPTIDE_1
[8-L-LYSINE,9-(1-AMINO-1-CYCLOPROPANECARBOXYLIC ACID)]VASOPRESSINPOLYPEPTIDE
JAPONICIN_B
| 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 |