UEG

4,5-bis(hydroxymethyl)-2-methyl-pyridin-3-ol

Created:2013-09-12
Last modified:  2024-09-27

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Chemical Details

Formal Charge0
Atom Count23
Chiral Atom Count0
Bond Count23
Aromatic Bond Count6
2D diagram of UEG
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Chemical Component Summary

Name4,5-bis(hydroxymethyl)-2-methyl-pyridin-3-ol
Systematic Name (OpenEye OEToolkits)4,5-bis(hydroxymethyl)-2-methyl-pyridin-3-ol
FormulaC8 H11 N O3
Molecular Weight169.178
TypeNON-POLYMER

Chemical Descriptors

TypeProgramVersionDescriptor
SMILESACDLabs12.01Oc1c(c(cnc1C)CO)CO
SMILESCACTVS3.385Cc1ncc(CO)c(CO)c1O
SMILESOpenEye OEToolkits1.9.2Cc1c(c(c(cn1)CO)CO)O
Canonical SMILESCACTVS3.385 Cc1ncc(CO)c(CO)c1O
Canonical SMILESOpenEye OEToolkits1.9.2 Cc1c(c(c(cn1)CO)CO)O
InChIInChI1.03 InChI=1S/C8H11NO3/c1-5-8(12)7(4-11)6(3-10)2-9-5/h2,10-12H,3-4H2,1H3
InChIKeyInChI1.03 LXNHXLLTXMVWPM-UHFFFAOYSA-N

Drug Info: DrugBank

DrugBank data are sourced from datasets licensed under a Creative Common's Attribution-NonCommercial 4.0 International License
DrugBank IDDB00165 
NamePyridoxine
Groups
  • approved
  • investigational
  • vet_approved
  • nutraceutical
DescriptionPyridoxine is the 4-methanol form of vitamin B6, an important water-soluble vitamin that is naturally present in many foods. As its classification as a vitamin implies, Vitamin B6 (and pyridoxine) are essential nutrients required for normal functioning of many biological systems within the body. While many plants and microorganisms are able to synthesize pyridoxine through endogenous biological processes, animals must obtain it through their diet. More specifically, pyridoxine is converted to pyridoxal 5-phosphate in the body, which is an important coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, and aminolevulinic acid. It's important to note that Vitamin B6 is the collective term for a group of three related compounds, pyridoxine, pyridoxal, and pyridoxamine, and their phosphorylated derivatives, pyridoxine 5'-phosphate, pyridoxal 5'-phosphate and pyridoxamine 5'-phosphate. Although all six of these compounds should technically be referred to as vitamin B6, the term vitamin B6 is commonly used interchangeably with just one of them, pyridoxine [A32836]. Vitamin B6, principally in its biologically active coenzyme form pyridoxal 5'-phosphate, is involved in a wide range of biochemical reactions, including the metabolism of amino acids and glycogen, the synthesis of nucleic acids, hemogloblin, sphingomyelin and other sphingolipids, and the synthesis of the neurotransmitters serotonin, dopamine, norepinephrine and gamma-aminobutyric acid (GABA) [A32837]. Pyridoxine is used medically for the treatment of vitamin B6 deficiency and for the prophylaxis of isoniazid-induced peripheral neuropathy (due to [DB00951]'s mechanism of action which competitively inhibits the action of pyridoxine in the above-mentioned metabolic functions). It is also used in combination with [DB00366] (as the commercially available product Diclectin) for the treatment of nausea and vomiting in pregnancy.
Synonyms
  • 5-hydroxy-6-methyl-3,4-pyridinedimethanol
  • Pyridoxine
  • 3-hydroxy-4,5-bis(hydroxymethyl)-2-methylpyridine
  • Pyridoxine hydrochloride
  • Vitamin B6
Brand Names
  • Poly-Vite Pediatric Oral Solution
  • Escavite Lq
  • American Plus Energy & Vitamin Drink
  • Formula Hh
  • Niacex B6
IndicationPyridoxine is indicated for the treatment of vitamin B6 deficiency and for the prophylaxis of [DB00951]-induced peripheral neuropathy. It is also approved by Health Canada for the treatment of nausea and vomiting in pregnancy in a combination product with [DB00366] (as the commercially available product Diclectin).
Categories
  • Alimentary Tract and Metabolism
  • Analogs/Derivatives
  • Antiinfectives for Systemic Use
  • Antimycobacterials
  • Diet, Food, and Nutrition
ATC-Code
  • J04AM08
  • A11HA02
CAS number65-23-6

Drug Targets

DrugBank data are sourced from datasets licensed under a Creative Common's Attribution-NonCommercial 4.0 International License
NameTarget SequencePharmacological ActionActions
Aromatic-L-amino-acid decarboxylaseMNASEFRRRGKEMVDYMANYMEGIEGRQVYPDVEPGYLRPLIPAAAPQEP...unknowncofactor
Pyridoxal kinaseMEEECRVLSIQSHVIRGYVGNRAATFPLQVLGFEIDAVNSVQFSNHTGYA...unknownligand
Cytochrome P450 1A1MLFPISMSATEFLLASVIFCLVFWVIRASRPQVPKGLKNPPGPWGWPLIG...unknowninhibitor
Pyridoxal kinaseMEEECRVLSIQSHVIRGYVGNRAATFPLQVLGFEIDAVNSVQFSNHTGYA...unknownsubstrate
ChronophinMARCERLRGAALRDVLGRAQGVLFDCDGVLWNGERAVPGAPELLERLARA...unknownsubstrate
View More
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 1054
ChEMBL CHEMBL1364
ChEBI CHEBI:16709
CCDC/CSD BITZAF