Compound
neurotensin-(1-7)
A peptide anion of neurotensin (1-7) resulting from the deprotonation of the carboxy groups of L-α-glutamyl and L-proline residues, and protonation of the side chain of L-lysyl group. It is the major species at pH 7.3.
Definition from ChEBI (CHEBI:147394), read 2026-09-23. CC BY 4.0.
CHEBI:147394ChEBI
Structure
No three-dimensional record for this entry.
- Class
- Organic compound, anion
- Formula
- C40H58N9O13
- Mass
- 872.954 g/mol
- Charge
- -1
- InChIKey
- BFBHOALZWJNUPJ-FLMSMKGQSA-M
- SMILES
- CC(C)C[C@H](NC(=O)[C@@H]1CCC(=O)N1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCC(=O)[O-])C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCC[NH3+])C(=O)N1CCC[C@H]1C(=O)[O-]
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence.
Reactions
1 reaction
neurotensin-(1-8)+waterneurotensin-(1-7)+L-arginine
Catalysed by ACE2
Reaction pageLeft to rightBalanced
Rhea RHEA:63572CC BY 4.0Reference data
Other names
10 names
Resolves to: neurotensin-(1-7)
- Also called
- L-Pyr-L-Leu-L-Tyr-L-Glu-L-Asn-L-Lys-L-Pro(1-)L-Pyr-L-Leu-L-Tyr-L-Glu-L-Asn-L-Lys-L-Pro(1−)L-pyroglutamyl-L-leucyl-L-tyrosyl-L-alpha-glutamyl-L-asparagyl-L-lysyl-L-proline(1-)L-pyroglutamyl-L-leucyl-L-tyrosyl-L-α-glutamyl-L-asparagyl-L-lysyl-L-proline(1−)neurotensin-(1-7)(1-)neurotensin-(1-7)(1−)Pyr-Leu-Tyr-Glu-Asn-Lys-Pro(1-)Pyr-Leu-Tyr-Glu-Asn-Lys-Pro(1−)
- Systematic name
- 5-oxo-L-prolyl-L-leucyl-L-tyrosyl-5-oxidanidyl-5-oxidanylidene-L-norvalyl-N(1)-{(2S)-6-azaniumyl-1-[(2S)-2-carboxylatopyrrolidin-1-yl]-1-oxohexan-2-yl}-L-aspartamide5-oxo-L-prolyl-L-leucyl-L-tyrosyl-5-oxidanidyl-5-oxidanylidene-L-norvalyl-N1-{(2S)-6-azaniumyl-1-[(2S)-2-carboxylatopyrrolidin-1-yl]-1-oxohexan-2-yl}-L-aspartamide