Substance

ID:510

Names and Identifiers
IUPAC Traditional name
niacin
IUPAC name
pyridine-3-carboxylic acid
Synonyms
niacinVitamin B3Nicotinic AcidNiacinAcidum NicotinicumM-Pyridinecarboxylic AcidNicotine AcidPyridylcarboxylic AcidAcide NicotiniquePyridinecarboxylic Acid3-Pyridinecarboxylic acidNAH
Brand Name
PP FactorNicorolNicosylNicylNipellenNyclinPeloninApelagrinNaotinNicanginNico-SpanNicocrisinaNicodelmineTinicPellagrinSk-NiacinVitaplex NNiconacidNiconazidNicosideNicoteneNicotilNicotinipcaSimcorDaskilNICONicacidNicotaminNicotinsaureP.P. FactorPellagra Preventive FactorTega-SpanNiaspanKyselina NikotinovaLinicNicocidinNicodanNiconatNicosan 3PevitonAkotinAnti-Pellagra VitaminBionicDavitamon PPDiacinNiacNicodonNicovasanNicovasenNicovelPellagraminDirektanEfacin
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Solubility
18 mg/mL at 25 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]
Hydrophobicity(logP)
0.4
Molecule Details
Drug Groups
approved; nutraceutical; investigational
Description
A water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is required by the body for the formation of coenzymes NAD and NADP. It has pellagra-curative, vasodilating, and antilipemic properties. [PubChem]
Indication
For the treatment of type IV and V hyperlipidemia. It is indicated as ajunctive therapy.
Pharmacology
Niacin and niacinamide are indicated for prevention and treatment of vitamin B3 deficiency states. Vitamin B3 (Niacin) also acts to reduce LDL cholesterol, triglycerides, and HDL cholesterol. The magnitude of individual lipid and lipoprotein responses may be influenced by the severity and type of underlying lipid abnormality. The increase in total HDL is associated with a shift in the distribution of HDL subfractions (as defined by ultra-centrifugation) with an increase in the HDL2:HDL3 ratio and an increase in apolipoprotein A-I content. Vitamin B3 (Niacin) treatment also decreases the serum levels of apolipoprotein B-100 (apo B), the major protein component of the VLDL (very low-density lipoprotein) and LDL fractions, and of lipoprotein-a, a variant form of LDL independently associated with coronary risk.
Toxicity
Nicotinic acid can cause vasodilation of cutaneous blood vessels resulting in increased blood flow, principally in the face, neck and chest. This produces the niacin- or nicotinic acid-flush. The niacin-flush is thought to be mediated via the prostaglandin prostacyclin. Histamine may also play a role in the niacin-flush. Flushing is the adverse reaction first observed after intake of a large dose of nicotinic acid, and the most bothersome one. LD50 7000 mg/kg (Rat)
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic
Absorption
Both nicotinic acid and nicotinamide are efficiently absorbed from the stomach and small intestine.
Half Life
20-45 minutes.
External Links
Molecular Spectra
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References
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