CHEBI:149488 - neurotensin (1-7)

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ChEBI Name neurotensin (1-7) ChEBI ID CHEBI:149488 Definition A 7 amino acid peptide fragment of neurotensin. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C40H59N9O13 Net Charge 0 Average Mass 873.962 Monoisotopic Mass 873.42323 InChI InChI=1S/C40H59N9O13/c1-21(2)18-27(46-34(55)24-12-14-32(52)43-24)36(57)47-28(19-22-8-10-23(50)11-9-22)37(58)44-25(13-15-33(53)54)35(56)48-29(20-31(42)51)38(59)45-26(6-3-4-16-41)39(60)49-17-5-7-30(49)40(61)62/h8-11,21,24-30,50H,3-7,12-20,41H2,1-2H3,(H2,42,51)(H,43,52)(H,44,58)(H,45,59)(H,46,55)(H,47,57)(H,48,56)(H,53,54)(H,61,62)/t24-,25-,26-,27-,28-,29-,30-/m0/s1 InChIKey BFBHOALZWJNUPJ-FLMSMKGQSA-N SMILES [C@@H]1(N(C([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC2=CC=C(O)C=C2)NC([C@@H](NC([C@H]3NC(=O)CC3)=O)CC(C)C)=O)=O)CCC(O)=O)=O)CC(N)=O)=O)CCCCN)=O)CCC1)C(O)=O Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing neurotensin (1-7) (CHEBI:149488) has role human metabolite (CHEBI:77746) neurotensin (1-7) (CHEBI:149488) is a peptide (CHEBI:16670) neurotensin (1-7) (CHEBI:149488) is conjugate acid of neurotensin (1-7)(1−) (CHEBI:147394) Incoming neurotensin (1-7)(1−) (CHEBI:147394) is conjugate base of neurotensin (1-7) (CHEBI:149488) IUPAC Name 5-oxo-L-prolyl-L-leucyl-L-tyrosyl-L-α-glutamyl-L-asparaginyl-L-lysyl-L-proline Synonyms Sources 5-oxo-L-Pro-L-Leu-L-Tyr-L-Glu-L-Asn-L-Lys-L-Pro ChEBI Glp-Leu-Tyr-Glu-Asn-Lys-Pro ChEBI <Glu-Leu-Tyr-Glu-Asn-Lys-Pro-OH ChEBI L-Pyr-L-Leu-L-Tyr-L-Glu-L-Asn-L-Lys-L-Pro ChEBI neurotensin (1-7) ChEBI neurotensin 1-7 ChEBI neurotensin-(1-7) ChEBI Pyr-Leu-Tyr-Glu-Asn-Lys-Pro ChEBI Citations Types Sources 11226674 PubMed citation Europe PMC 12065070 PubMed citation Europe PMC 3301344 PubMed citation Europe PMC 6252013 PubMed citation Europe PMC 8472756 PubMed citation Europe PMC Last Modified 17 April 2020