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Nicotinyl alcohol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Nicotinyl alcohol
Clinical data
Other namesRoniacol; Roniacol tartrate; Nicotinyl tartrate;[1] Nicotinyl alcohol tartrate; Nicotinic alcohol; Pyridylcarbinol
AHFS/Drugs.comMonograph
ATC code
Identifiers
  • (Pyridin-3-yl)methanol
CAS Number
PubChemCID
ChemSpider
UNII
ChEBI
CompTox Dashboard(EPA)
ECHA InfoCard100.002.604Edit this at Wikidata
Chemical and physical data
FormulaC6H7NO
Molar mass109.128 g·mol−1
3D model (JSmol)
  • OCc1cccnc1
  • InChI=1S/C6H7NO/c8-5-6-2-1-3-7-4-6/h1-4,8H,5H2 ☒N
 ☒NcheckY (what is this?)  (verify)

Nicotinyl alcohol (pyridylcarbinol) is aniacin derivative used as ahypolipidemic agent and as avasodilator. It causes flushing and may decrease blood pressure.[2]

It appears as a crystal that dissolves in water and alcohol with ease, also soluble in ether; melting range 147–148 °C.[citation needed]

Nicotinic acid is a brief peripheral vasodilator; this compound was made to make its action longer and effective. It provokes cutaneous flushing in head and upper thorax with heat, but with no major effects in blood pressure. It is used in peripheral vascular diseases, likearteriosclerosis obliterans,[3]Raynaud's disease,[4] thromboangiitis obliterans (Buerger's disease),[5] arterial embolism,chilblains or migraine associated with vascular spasm.

Fischer and Tebrock worked with this drug in more than two hundred patients for more than three years, achieving effective improvements, mainly in symptoms related tointermittent claudication,[6] ulcer healing and others.[7]

Derivatives

[edit]

At least a couple of uses for this agent were discovered over the years:

  1. Eniclobrate
  2. Mepiroxol
  3. Nicofibrate
  4. Pantenicate (Topanicate, MG 28362)

References

[edit]
  1. ^Norwood WF (1963). "Vasodilator Effects of Nicotinyl Tartrate (Roniacol Tartrate)".JAMA.186: 1013.doi:10.1001/jama.1963.03710110065012.PMID 14066712.
  2. ^"Ronicol Retard".Medical Dictionary Online. 2012. Archived fromthe original on June 14, 2011. RetrievedJuly 27, 2012.
  3. ^Richter IH, Fogel M, Fabricant H (1951). "An evaluation of roniacol tartrate in arteriosclerosis obliterans".New York State Journal of Medicine.51 (10):1303–4.PMID 14843421.
  4. ^"Medical Dictionary, Dictionary of medicine and human biology, medical, biological and chemical terminology".www.theodora.com.
  5. ^"Buergers disease by dr .ravinder narwal". July 7, 2011. page 18.
  6. ^Gillhespy, RO (1957)."Nicotinyl Alcohol Tartrate in Intermittent Claudication".British Medical Journal.18 (2):207–208.doi:10.1136/bmj.1.5012.207.PMC 1974214.PMID 13383231.
  7. ^Fisher MM, Tebrock HW (1953). "Nicotinic alcohol (roniacol) in peripheral vascular diseases and allied conditions: its use and limitations".New York State Journal of Medicine.53 (1):65–8.PMID 13025721.
GI tract
Cholesterol absorption inhibitors,NPC1L1
Bile acid sequestrants/resins (LDL)
Liver
Statins (HMG-CoA reductase,LDL)
Niacin and derivatives (HDL andLDL)
MTTP inhibitors (VLDL)
ATP citrate lyase inhibitors (LDL)
Thyromimetics (VLDL)
Blood vessels
PPAR agonists (LDL)
Fibrates
Others
CETP inhibitors (HDL)
PCSK9 inhibitors (LDL)
ANGPTL3 inhibitors (LDL/HDL)
Combinations
Other
Phenylethanolamine derivatives
Alpha blockers
Nicotinic acid and derivatives
Purine derivatives
Ergot alkaloids
Other peripheral vasodilators
Retrieved from "https://en.wikipedia.org/w/index.php?title=Nicotinyl_alcohol&oldid=1332194570"
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