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Phenopicolinic acid

From Wikipedia, the free encyclopedia
Phenopicolinic acid
Names
Preferred IUPAC name
5-[(4-Hydroxyphenyl)methyl]pyridine-2-carboxylic acid
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C13H11NO3/c15-11-4-1-9(2-5-11)7-10-3-6-12(13(16)17)14-8-10/h1-6,8,15H,7H2,(H,16,17)
    Key: SJBFZHNCSGBLEK-UHFFFAOYSA-N
  • InChI=1/C13H11NO3/c15-11-4-1-9(2-5-11)7-10-3-6-12(13(16)17)14-8-10/h1-6,8,15H,7H2,(H,16,17)
    Key: SJBFZHNCSGBLEK-UHFFFAOYAB
  • C1=CC(=CC=C1CC2=CN=C(C=C2)C(=O)O)O
Properties
C13H11NO3
Molar mass229.235 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Phenopicolinic acid is adopamine beta hydroxylaseinhibitor.[1]

References

[edit]
  1. ^Nakamura, Teruya; Yasuda, Hideyuki; Obayashi, Akira; Tanabe, Osamu; Matsumura, Shingo; Ueda, Fusao; Ohata, Katsuya (Jun 1975)."Phenopicolinic acid, a new microbial product inhibiting dopamine beta-hydroxylase".J Antibiot (Tokyo).28 (6):477–8.doi:10.7164/antibiotics.28.477.PMID 1150540.


Non-specific
AAADTooltip Aromatic L-amino acid decarboxylase
MAOTooltip Monoamine oxidase
Phenethylamines
(dopamine,epinephrine,
norepinephrine)
PAHTooltip Phenylalanine hydroxylase
THTooltip Tyrosine hydroxylase
DBHTooltip Dopamine beta-hydroxylase
PNMTTooltip Phenylethanolamine N-methyltransferase
COMTTooltip Catechol-O-methyl transferase
Tryptamines
(serotonin,melatonin)
TPHTooltip Tryptophan hydroxylase
AANATTooltip Serotonin N-acetyl transferase
ASMTTooltip Acetylserotonin O-methyltransferase
Histamine
HDCTooltip Histidine decarboxylase
HNMTTooltip Histamine N-methyltransferase
DAOTooltip Diamine oxidase
Retrieved from "https://en.wikipedia.org/w/index.php?title=Phenopicolinic_acid&oldid=1252435249"
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