CHEBI:139154 - AZD1979

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ChEBI Name AZD1979
ChEBI ID CHEBI:139154
Definition A carboxamide resulting from the formal condensation of the carboxy group of 5-(p-methoxyphenyl)-1,3,4-oxadiazole-2-carboxylic acid with the amino group of 3-phenoxyazetidine and in which the phenoxy group has been substituted at the para- position by a 2-oxa-6-azaspiro[3.3]heptan-6-ylmethyl group. It is a melanin concentrating hormone receptor 1 (MCHr1) antagonist.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C25H26N4O5
Net Charge 0
Average Mass 462.499
Monoisotopic Mass 462.19032
InChI InChI=1S/C25H26N4O5/c1-31-19-8-4-18(5-9-19)22-26-27-23(34-22)24(30)29-11-21(12-29)33-20-6-2-17(3-7-20)10-28-13-25(14-28)15-32-16-25/h2-9,21H,10-16H2,1H3
InChIKey BKKPIQPFRAPEAY-UHFFFAOYSA-N
SMILES C1(CN(C1)C(C=2OC(=NN2)C3=CC=C(C=C3)OC)=O)OC4=CC=C(C=C4)CN5CC6(C5)COC6
Roles Classification
Biological Role(s): melanin-concentrating hormone receptor antagonist
An antagonist that attaches to and blocks melanin-concentrating hormone receptors.
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ChEBI Ontology
Outgoing AZD1979 (CHEBI:139154) has role melanin-concentrating hormone receptor antagonist (CHEBI:139155)
AZD1979 (CHEBI:139154) is a N-acylazetidine (CHEBI:46959)
AZD1979 (CHEBI:139154) is a aromatic ether (CHEBI:35618)
AZD1979 (CHEBI:139154) is a azaspiro compound (CHEBI:35624)
AZD1979 (CHEBI:139154) is a carboxamide (CHEBI:37622)
AZD1979 (CHEBI:139154) is a oxadiazole (CHEBI:46685)
AZD1979 (CHEBI:139154) is a oxaspiro compound (CHEBI:37948)
AZD1979 (CHEBI:139154) is a oxetanes (CHEBI:38784)
AZD1979 (CHEBI:139154) is conjugate base of AZD1979(1+) (CHEBI:138980)
Incoming AZD1979 oxetane hydrolysis product (CHEBI:139019) has functional parent AZD1979 (CHEBI:139154)
AZD1979(1+) (CHEBI:138980) is conjugate acid of AZD1979 (CHEBI:139154)
IUPAC Name
[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]{3-[4-(2-oxa-6-azaspiro[3.3]heptan-6-ylmethyl)phenoxy]azetidin-1-yl}methanone
Synonyms Sources
AZD 1979 ChemIDplus
AZD-1979 ChemIDplus
Manual Xrefs Databases
CPD-20318 MetaCyc
WO2010125390 Patent
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Registry Numbers Types Sources
1254035-84-1 CAS Registry Number ChemIDplus
20834832 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
26741166 PubMed citation Europe PMC
27256986 PubMed citation Europe PMC
27400775 PubMed citation Europe PMC
28556607 PubMed citation Europe PMC
Last Modified
28 November 2017