N-[(BENZYLOXY)-CARBONYL]-L-LEUCYL-2-METHYLALANYL-L-PROLYL-L-VALYL-2-METHYLALANINYL-2-METHYLALANYL-0-(5)-BENZYL-L-GLUTAM-1-YL-L-GLUTAMINYL-L-PHENYLALANINOL;COMP
Compound with spectra: 1 NMR
![N-[(BENZYLOXY)-CARBONYL]-L-LEUCYL-2-METHYLALANYL-L-PROLYL-L-VALYL-2-METHYLALANINYL-2-METHYLALANYL-0-(5)-BENZYL-L-GLUTAM-1-YL-L-GLUTAMINYL-L-PHENYLALANINOL;COMP](/api/compound/E96d827jlVZ.png?ph=true&h=300&w=458 "N-[(BENZYLOXY)-CARBONYL]-L-LEUCYL-2-METHYLALANYL-L-PROLYL-L-VALYL-2-METHYLALANINYL-2-METHYLALANYL-0-(5)-BENZYL-L-GLUTAM-1-YL-L-GLUTAMINYL-L-PHENYLALANINOL;COMP")
| SpectraBase Compound ID | E96d827jlVZ |
|---|---|
| InChI | InChI=1S/C62H88N10O14/c1-38(2)33-46(67-59(84)86-37-42-25-18-13-19-26-42)53(78)69-62(9,10)58(83)72-32-20-27-47(72)54(79)68-50(39(3)4)55(80)70-61(7,8)57(82)71-60(5,6)56(81)66-45(29-31-49(75)85-36-41-23-16-12-17-24-41)52(77)65-44(28-30-48(63)74)51(76)64-43(35-73)34-40-21-14-11-15-22-40/h11-19,21-26,38-39,43-47,50,73H,20,27-37H2,1-10H3,(H2,63,74)(H,64,76)(H,65,77)(H,66,81)(H,67,84)(H,68,79)(H,69,78)(H,70,80)(H,71,82)/t43?,44-,45?,46-,47?,50-/m1/s1 |
| InChIKey | DFRXSMKEOZPQGL-HCIFOWQGSA-N |
| Mol Weight | 1197.4 g/mol |
| Molecular Formula | C62H88N10O14 |
| Exact Mass | 1196.648148 g/mol |
| Enantiomer InChIKey | DFRXSMKEOZPQGL-DWSKBFLVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
TYLOPEPTIN-B;AC-L-TRP-L-VAL-L-AIB-L-AIB-L-ALA-L-GLU-L-ALA-L-AIB-L-SER-L-AIB-L-ALA-L-LEU-L-AIB-L-GLN-L-LEUNOL
OXYTOCIN;OXT
1-[19-amino-7-(2-amino-2-keto-ethyl)-10-(3-amino-3-keto-propyl)-16-(4-hydroxybenzyl)-6,9,12,15,18-pentaketo-13-sec-butyl-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]-N-[1-[(2-amino-2-keto-ethyl)carbamoyl]-3-methyl-butyl]pyrrolidine-2-carboxamid
Mesotocin
ROFXUKMWVLLFCV-UHFFFAOYSA-N
XENTRIVALPEPTIDE_A
MICROTENIN_C;CYClO-(PRO-(1)-TYR-ASN-PHE-PRO-(2)-LEU-PRO-(3)-ILE)
GLABRIN-D;CYCLO-(PROLYL-PROLYL-VALYL-TYROSYL-GLYCYL-PROLYL-GLUTAMYL)
Glumitocin
DICHOTOMIN-H;CYClO-(-ALA-PRO-THR-PHE-TYR-PRO-LEU-ILE-)
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Peptides Containing α,α‐Disubstituted α‐Amino Acids by the Azirine/Oxazolone Method: The (12–20)‐Nonapeptide of the Ionophore Alamethicin | Helvetica Chimica Acta | 1990 |