Chemistry:Nizatidine

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Short description: Chemical compound
Nizatidine
Nizatidine.svg
Clinical data
Trade namesAxid, Tazac
AHFS/Drugs.comMonograph
MedlinePlusa694030
License data
Pregnancy
category
  • AU: B3
Routes of
administration
By mouth
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
  • UK: POM (Prescription only)
  • US: OTC / Rx-only
Pharmacokinetic data
Bioavailability>70%
Protein binding35%
MetabolismLiver
Elimination half-life1–2 hours
ExcretionKidney
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC12H21N5O2S2
Molar mass331.45 g·mol−1
3D model (JSmol)
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Nizatidine is a histamine H2 receptor antagonist that inhibits stomach acid production, and is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease.[1]

It was patented in 1980 and approved for medical use in 1988.[2][3] It was developed by Eli Lilly.

Medical use

Main page: Chemistry:H2 antagonist

Nizatidine is used to treat duodenal ulcers, gastric ulcers, and gastroesophageal reflux disease (GERD/GORD), and to prevent stress ulcers.[4]

Adverse effects

Side effects are uncommon, usually minor, and include diarrhea, constipation, fatigue, drowsiness, headache, and muscle aches.[4]

History and development

Nizatidine was developed by Eli Lilly, and was first marketed in 1988.[2] It is considered to be equipotent with ranitidine and differs by the substitution of a thiazole ring in place of the furan ring in ranitidine. In September 2000, Eli Lilly announced they would sell the sales and marketing rights for Axid to Reliant Pharmaceuticals.[5] Subsequently, Reliant developed the oral solution of Axid, marketing this in 2004, after gaining approval from the U.S. Food and Drug Administration (FDA).[6] However, a year later, they sold rights of the Axid Oral Solution (including the issued patent[7] protecting the product) to Braintree Laboratories.[8]

Society and culture

Brand names

Brand names include Tazac and Axid.

References

  1. "[Nizatidine]" (in it). Medicina 9 (1): 93–96. 1989. PMID 2567957. 
  2. 2.0 2.1 "Nizatidine: FDA-Approved Drugs". https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=019508. 
  3. (in en) Analogue-based Drug Discovery. John Wiley & Sons. 2006. p. 44. ISBN 9783527607495. https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA444. 
  4. 4.0 4.1 "Nizatidine". LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. NCBI Bookshelf. 25 January 2018. NBK548387. https://www.ncbi.nlm.nih.gov/books/NBK548387/. Retrieved 19 March 2020. 
  5. "Eli Lilly and Company and Reliant Pharmaceuticals Announce Agreement for U.S. Sales and Marketing Rights to Axid(R)". Encyclopedia.com. 7 September 2000. http://www.encyclopedia.com/doc/1G1-65062714.html?Q=%22axid%22. 
  6. "Reliant Pharmaceuticals to Launch AxidŽ Oral Solution". Reliant Pharmaceuticals, LLC. 26 July 2004. http://www.reliantrx.com/investor/press_releases/072604.htm. 
  7. Bobotas G, Fawzy AA, "Liquid pharmaceutical composition", US patent 6930119, issued 24 June 2005, assigned to Reliant Pharmaceuticals, LLC
  8. "Reliant Pharmaceuticals Announces the Sale of Axid® Oral Solution to Braintree Laboratories". Reliant Pharmaceuticals, LLC. http://www.reliantrx.com/investor/press_releases/063005.htm.