CHEBI:6762 - mepyramine

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ChEBI Name mepyramine
ChEBI ID CHEBI:6762
Definition An ethylenediamine derivative that is ethylenediamine in which one of the amino nitrogens is substituted by two methyl groups and the remaining amino nitrogen is substituted by a 4-methoxybenzyl and a pyridin-2-yl group.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C17H23N3O
Net Charge 0
Average Mass 285.38414
Monoisotopic Mass 285.18411
InChI InChI=1S/C17H23N3O/c1-19(2)12-13-20(17-6-4-5-11-18-17)14-15-7-9-16(21-3)10-8-15/h4-11H,12-14H2,1-3H3
InChIKey YECBIJXISLIIDS-UHFFFAOYSA-N
SMILES COc1ccc(CN(CCN(C)C)c2ccccn2)cc1
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): H1-receptor antagonist
H1-receptor antagonists are the drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine.
Application(s): H1-receptor antagonist
H1-receptor antagonists are the drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine.
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ChEBI Ontology
Outgoing mepyramine (CHEBI:6762) has role H1-receptor antagonist (CHEBI:37955)
mepyramine (CHEBI:6762) is a aromatic ether (CHEBI:35618)
mepyramine (CHEBI:6762) is a ethylenediamine derivative (CHEBI:31577)
IUPAC Name
N-(4-methoxybenzyl)-N',N'-dimethyl-N-pyridin-2-ylethane-1,2-diamine
Synonyms Sources
Mepyramine KEGG COMPOUND
N',N'-dimethyl-N-(p-methoxybenzyl)-N-(2-pyridyl)ethylenediamine NIST Chemistry WebBook
N-(p-methoxybenzyl)-N',N'-dimethyl-N-(α-pyridyl)ethylenediamine NIST Chemistry WebBook
N-[(4-methoxyphenyl)methyl]-N',N'-dimethyl-N-2-pyridinyl-1,2-ethanediamine NIST Chemistry WebBook
pyranisamine ChemIDplus
Pyrilamine KEGG COMPOUND
Manual Xrefs Databases
2331 DrugCentral
C11798 KEGG COMPOUND
D08183 KEGG DRUG
DB06691 DrugBank
HMDB0015639 HMDB
LSM-4206 LINCS
Pyrilamine Wikipedia
View more database links
Registry Numbers Types Sources
269019 Beilstein Registry Number Beilstein
269019 Reaxys Registry Number Reaxys
877512 Gmelin Registry Number Gmelin
91-84-9 CAS Registry Number NIST Chemistry WebBook
91-84-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
24316866 PubMed citation Europe PMC
24813183 PubMed citation Europe PMC
Last Modified
22 February 2017