CHEBI:137728 - tetragastrin

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name tetragastrin
Definition A tetrapeptide composed of L-tryptophan, L-methione, L-aspartic acid and L-phenylalaninamide residues joined in sequence.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:32210
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C29H36N6O6S
Net Charge 0
Average Mass 596.700
Monoisotopic Mass 596.24170
InChI InChI=1S/C29H36N6O6S/c1-42-12-11-22(33-27(39)20(30)14-18-16-32-21-10-6-5-9-19(18)21)28(40)35-24(15-25(36)37)29(41)34-23(26(31)38)13-17-7-3-2-4-8-17/h2-10,16,20,22-24,32H,11-15,30H2,1H3,(H2,31,38)(H,33,39)(H,34,41)(H,35,40)(H,36,37)/t20-,22-,23-,24-/m0/s1
SMILES C(=O)([C@@H](N)CC1=CNC2=C1C=CC=C2)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CC=3C=CC=CC3)C(N)=O)CC(O)=O)CCSC
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) See: PubMed
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).
Application(s): anxiogenic
Any psychotropic drug that induces anxiety or panic.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing tetragastrin (CHEBI:137728) has role anxiogenic (CHEBI:137736)
tetragastrin (CHEBI:137728) has role human metabolite (CHEBI:77746)
tetragastrin (CHEBI:137728) is a peptidyl amide (CHEBI:15722)
tetragastrin (CHEBI:137728) is a tetrapeptide (CHEBI:48030)
Synonyms Sources
CCRIS 3246 ChemIDplus
Cholecystokinin tetrapeptide ChemIDplus
cholecystokinin-4 ChEBI
Gastrin tetrapeptide ChemIDplus
Gastrin tetrapeptide amide ChemIDplus
L-Trp-L-Met-L-Asp-L-Phe-NH2 ChEBI
L-tryptophyl-L-methionyl-L-aspartyl-L-phenylalaninamide ChEBI
Trp-Met-Asp-Phe-NH2 ChEBI
Manual Xrefs Databases
CCK-4 Wikipedia
HMDB0005775 HMDB
View more database links
Registry Numbers Types Sources
1947-37-1 CAS Registry Number ChemIDplus
24193542 Reaxys Registry Number Reaxys
4223651 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
20198494 PubMed citation Europe PMC
20387390 PubMed citation Europe PMC
22414867 PubMed citation Europe PMC
22632477 PubMed citation Europe PMC
22939006 PubMed citation Europe PMC
23059050 PubMed citation Europe PMC
23463151 PubMed citation Europe PMC
24342768 PubMed citation Europe PMC
24939759 PubMed citation Europe PMC
25106129 PubMed citation Europe PMC
25522396 PubMed citation Europe PMC
26235955 PubMed citation Europe PMC
26752621 PubMed citation Europe PMC
27871026 PubMed citation Europe PMC
28328228 PubMed citation Europe PMC
Last Modified
10 August 2017