4-aminopyridine-3-methanol (CHEBI:149772)

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ChEBI Name	4-aminopyridine-3-methanol

ChEBI ID	CHEBI:149772

Definition	An aminopyridine that is 4-aminopyridine which is substituted by a hydroxymethyl group at position 3. It is a potassium channel blocker which restores axonal conduction after spinal cord injury.

Stars	This entity has been manually annotated by the ChEBI Team.

Submitter	Ceri

Supplier Information

Download	Molfile XML SDF

Formula

C6H8N2O

Net Charge

Average Mass

124.143

Monoisotopic Mass

124.06366

InChI

InChI=1S/C6H8N2O/c7-6-1-2-8-3-5(6)4-9/h1-3,9H,4H2,(H2,7,8)

InChIKey

WNBVEYMTVDMSFZ-UHFFFAOYSA-N

SMILES

C=1C=NC=C(C1N)CO

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):	potassium channel blocker An agent that inhibits cell membrane glycoproteins that are selectively permeable to potassium ions.

ChEBI Ontology
Outgoing	4-aminopyridine-3-methanol (CHEBI:149772) has functional parent 4-aminopyridine (CHEBI:34385) 4-aminopyridine-3-methanol (CHEBI:149772) has role potassium channel blocker (CHEBI:50509) 4-aminopyridine-3-methanol (CHEBI:149772) is a aminopyridine (CHEBI:38207) 4-aminopyridine-3-methanol (CHEBI:149772) is a aromatic amine (CHEBI:33860) 4-aminopyridine-3-methanol (CHEBI:149772) is a aromatic primary alcohol (CHEBI:33857)

IUPAC Name

(4-aminopyridin-3-yl)methanol

Synonyms	Sources
4-amino-3-(hydroxymethyl)pyridine	ChEBI
4-amino-3-pyridinemethanol	ChEBI
4-AP-3-MeOH	SUBMITTER

Registry Number	Type	Source
138116-34-4	CAS Registry Number	ChEBI

Last Modified

20 May 2020