METHYL-(2S,4S)-N-((2S)-N-{(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL)-PROLYL}-4-HYDROXYPROLINATE
Compound with spectra: 1 NMR
![METHYL-(2S,4S)-N-((2S)-N-{(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL)-PROLYL}-4-HYDROXYPROLINATE](/api/compound/EmVULjRFWOI.png?ph=true&h=300&w=458 "METHYL-(2S,4S)-N-((2S)-N-{(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL)-PROLYL}-4-HYDROXYPROLINATE")
| SpectraBase Compound ID | EmVULjRFWOI |
|---|---|
| InChI | InChI=1S/C19H28ClN3O6/c1-11(20)16(25)21-7-3-5-13(21)17(26)22-8-4-6-14(22)18(27)23-10-12(24)9-15(23)19(28)29-2/h11-15,24H,3-10H2,1-2H3/t11-,12?,13-,14-,15?/m0/s1 |
| InChIKey | BCJPTJMDYKKPFY-COYCRWBJSA-N |
| Mol Weight | 429.9 g/mol |
| Molecular Formula | C19H28ClN3O6 |
| Exact Mass | 429.166663 g/mol |
| Enantiomer InChIKey | BCJPTJMDYKKPFY-HNBOJAAESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-(2S,4S)-N-[(2S)-N-[(2S)-N-[(2S)-2-CH”OROPROPIONYL]-PROPYL]-PROPYL]-4-MERCAPTOPROLINATE
(2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTANOYL-L-LEUCYL-L-PROLYL-L-PROLINE;PROBESTIN
MR-387B
METHYL-(2S.4S)-N-[(2R)-N-[(2S)-N-[(2S)-2-CHLOROPROPIONYL]-PROLYL]-ALANYL]-4-(ACETYLTHIO)-PROLINATE
Gly-lys-hyp-gly-glu-hyp-gly-pro-lysine (cp9)
2-benzyl-1,4-dioxooctahydro-N,N-3-triethylpyrrolo[1,2-a]pyrazine-6-carboxamide
(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
| Title | Journal or Book | Year |
|---|---|---|
| Design, construction and properties of peptide N-terminal cap templates devised to initiate α-helices. Part 1. Caps derived from N-(4-chlorobutyryl)-(2S )-Pro-(2S )-Pro-(2S )-Ala-OMe and N-[(2S )-2-chloropropionyl]-(2S )-Pro-(2S )-Pro-(2S,4S )-4-hydroxyPro-OMe | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |