Ketcher 05202010142D 1   1.00000     0.00000     0

  9  9  0     0  0            999 V2000
    7.1945   -7.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1945   -8.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0605   -9.4603    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9266   -8.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9266   -7.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0605   -7.4603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0605   -6.4603    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.7927   -7.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6586   -7.9604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0     0  0
  2  3  2  0     0  0
  3  4  1  0     0  0
  4  5  2  0     0  0
  5  6  1  0     0  0
  6  1  2  0     0  0
  6  7  1  0     0  0
  5  8  1  0     0  0
  8  9  1  0     0  0
M  END
> <ID>
CHEBI:149772

> <NAME>
4-aminopyridine-3-methanol

> <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.

> <STAR>
3

> <SYNONYM>
4-AP-3-MeOH; 4-amino-3-pyridinemethanol; 4-amino-3-(hydroxymethyl)pyridine

> <IUPAC_NAME>
(4-aminopyridin-3-yl)methanol

> <FORMULA>
C6H8N2O

> <MASS>
124.143

> <MONOISOTOPIC_MASS>
124.06366

> <CHARGE>
0

> <SMILES>
C=1C=NC=C(C1N)CO

> <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

> <CAS_REGISTRY_NUMBER>
138116-34-4

> <PUBMED_CITATION>
19923250; 21093437; 22314968; 25143174; 26581866; 28817801; 29228863; 32009855

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