Drug General Information |
Drug ID |
D0L7RB
|
Former ID |
DNC006145
|
Drug Name |
1-(4-hydroxyphenyl)prop-2-en-1-one
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C9H8O2
|
Canonical SMILES |
C=CC(=O)C1=CC=C(C=C1)O
|
InChI |
1S/C9H8O2/c1-2-9(11)7-3-5-8(10)6-4-7/h2-6,10H,1H2
|
InChIKey |
NKPPNPJUBLEKAD-UHFFFAOYSA-N
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
4-aminobutyrate aminotransferase, mitochondrial |
Target Info |
Inhibitor |
[1]
|
Succinate semialdehyde dehydrogenase, mitochondrial |
Target Info |
Inhibitor |
[1]
|
BioCyc Pathway
|
GABA shunt
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Valine degradation
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Beta-alanine degradation
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4-aminobutyrate degradationGLUDEG-I-PWY:GABA shunt
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4-aminobutyrate degradation
|
KEGG Pathway
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Alanine, aspartate and glutamate metabolism
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Valine, leucine and isoleucine degradation
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beta-Alanine metabolism
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Propanoate metabolism
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Butanoate metabolism
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Metabolic pathways
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GABAergic synapsehsa00250:Alanine, aspartate and glutamate metabolism
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PANTHER Pathway
|
Aminobutyrate degradation
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Pyrimidine Metabolism
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Gamma-aminobutyric acid synthesisP02726:Aminobutyrate degradation
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Gamma-aminobutyric acid synthesis
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PathWhiz Pathway
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Aspartate Metabolism
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Glutamate Metabolism
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Beta-Alanine Metabolism
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Valine, Leucine and Isoleucine Degradation
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Propanoate MetabolismPW000003:Glutamate Metabolism
|
WikiPathways
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GABA synthesis, release, reuptake and degradation
|
Alanine and aspartate metabolismWP2685:GABA synthesis, release, reuptake and degradation
|
References |
REF 1 | Bioorg Med Chem Lett. 2006 Feb;16(3):592-5. Epub 2005 Nov 14.Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives. |