Chemistry:Cefdinir

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Short description: Chemical compound
Cefdinir
Cefdinir.svg
Clinical data
PronunciationSEF-di-nir
Trade namesCefzon, Omnicef, others
AHFS/Drugs.comMonograph
MedlinePlusa698001
License data
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability16% to 21% (dose-dependent)
Protein binding60% to 70%
MetabolismNegligible
Elimination half-life1.7 ± 0.6 hours
ExcretionKidney
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC14H13N5O5S2
Molar mass395.41 g·mol−1
3D model (JSmol)
Melting point170 °C (338 °F) (dec.)
  (verify)

Cefdinir, sold under the brand name Omnicef among others, is an antibiotic used to treat pneumonia, otitis media, strep throat, and cellulitis.[1] It is a less preferred option for pneumonia, otitis media, and strep throat which may be used in those with a severe allergy to penicillin.[1] It is taken by mouth.[1]

Common side effects include diarrhea, nausea, and a skin rash.[1] Serious side effects may include Clostridioides difficile infection, anaphylaxis, and Stevens–Johnson syndrome.[1] Use in pregnancy and breastfeeding is believed to be safe but has not been well studied.[2] It is a third-generation cephalosporin and works by interfering with a bacteria's ability to make a cell wall resulting in its death.[1]

It was patented in 1979 and approved for medical use in 1991.[3] It is available as a generic medication.[1] In 2020, it was the 228th most commonly prescribed medication in the United States, with more than 2 million prescriptions.[4][5]

Medical uses

Therapeutic uses of cefdinir include otitis media, soft tissue infections, and respiratory tract infections, including sinusitis, strep throat (note: no documented resistance of Group A Streptococcus to penicillin has ever been reported, and penicillin or amoxicillin is preferred except in penicillin allergic patients), community-acquired pneumonia, and acute exacerbations of bronchitis.

Susceptible organisms

Cefdinir is a bactericidal antibiotic of the cephalosporin class of antibiotics. It can be used to treat infections caused by several Gram-negative and Gram-positive bacteria.

Bacterial susceptibility and resistance

Cefdinir is a broad-spectrum antibiotic and has been used to treat infections of the respiratory tract including pneumonia, sinusitis, and bronchitis. The following represents MIC susceptibility data for a few medically significant microorganisms.[6]

  • Haemophilus influenzae: 0.05 - 4 μg/ml
  • Streptococcus pneumoniae: 0.006 - 64 μg/ml
  • Streptococcus pyogenes: ≤0.004 - 2 μg/ml

Side effects

Side effects include diarrhea, vaginal infections or inflammation, nausea, headache, and abdominal pain."[7]

It is also one of the medications that can cause toxic epidermal necrolysis or Stevens–Johnson syndrome.[8]

The pediatric version of cefdinir can bind to iron in the digestive tract; in rare cases, this causes a rust or red discoloration of the stool. Blood typically appears dark brown or black in stool, and testing may confirm which is present. If the reddish stool is accompanied by abdominal pain, weight loss, diarrhea, etc., a Clostridioides difficile infection caused by the antibiotic could be signified.

Mechanism of action

Main page: Chemistry:Cephalosporin

Society and culture

Economics

As of 2008, cefdinir was the highest-selling cephalosporin antibiotic in the United States, with more than $585 million in retail sales of its generic versions.[9][needs update]

Available forms

Cefdinir is administered orally. It is available as capsules and a suspension. Dosage, schedule, and duration of therapy varies according to the type of infection.

Warner-Lambert licensed the drug for marketing in US from Fujisawa.[10] Abbott obtained U.S. marketing rights to cefdinir in December 1998 through an agreement with Warner-Lambert Company.[11] It was approved by the FDA on December 4, 1997.[12] It is available in US as Omnicef by Abbott Laboratories and in India as Cednir by Abbott, Kefnir by Glenmark, Cefdair by Xalra Pharma and Cefdiel by Ranbaxy.

Synthesis

Cefdinir synthesis:[13][14][15] Improved prepn:[16]

Acylation of the primary amine 1 with 4-bromo-3-oxobutanoyl bromide (2) leads to the amide (3). The active methylene group in that product is then nitrosated with sodium nitrite; the initial product spontaneously tautomerizes to afford the oxime (4). The bromoketone array in that intermediate constitutes a classical starting function for construction of thiazoles. Reaction of 4 with thiourea thus leads to formation of an aminothiazole moiety. Thus there is obtained the antibiotic cefdinir (5).

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 "Cefdinir Monograph for Professionals" (in en). American Society of Health-System Pharmacists. https://www.drugs.com/monograph/cefdinir.html. 
  2. ↑ "Cefdinir Use During Pregnancy" (in en). https://www.drugs.com/pregnancy/cefdinir.html. 
  3. ↑ (in en) Analogue-based Drug Discovery. John Wiley & Sons. 2006. p. 49X. ISBN 9783527607495. https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA49X. 
  4. ↑ "The Top 300 of 2020". https://clincalc.com/DrugStats/Top300Drugs.aspx. 
  5. ↑ "Cefdinir - Drug Usage Statistics". https://clincalc.com/DrugStats/Drugs/Cefdinir. 
  6. ↑ "Susceptibility and Minimum Inhibitory Concentration (MIC) Data". October 14, 2015. http://www.toku-e.com/Assets/MIC/Cefdinir.pdf. 
  7. ↑ "Omnicef capsules Patient Information". Abbott Laboratories. February 2004. http://www.rxabbott.com/pdf/omnicef_capsules_patient_friendly.pdf. 
  8. ↑ "Omnicef manufacturer's packet insert". FDA. http://www.accessdata.fda.gov/drugsatfda_docs/label/1999/50739S2LBL.pdf. 
  9. ↑ "2008 Top 200 generic drugs by retail dollars". http://drugtopics.modernmedicine.com/drugtopics/data/articlestandard//drugtopics/192009/597086/article.pdf.  (399.4 KB). Drug Topics (May 26, 2009). Retrieved on July 24, 2009.
  10. ↑ "Document". elsevierbi.com. http://www.elsevierbi.com/publications/the-pink-sheet/52/005/comprecin-has-excellent-chance-to-reach-us-market-this-year-dupont-prophenytoin-crosslicense-deal?p=1. 
  11. ↑ "Medicis.com - Medicis Pharmaceutical Corporation". globenewswire.com. http://www.globenewswire.com/newsarchive/mrx/pages/news_releases.html?d=94045. 
  12. ↑ "Cefdinir medical facts from Drugs.com". drugs.com. https://www.drugs.com/mtm/cefdinir.html. 
  13. ↑ Takaya T, et al., BE patent 897864; eidem, U.S. Patent 4,559,334 (1984, 1985 both to Fujisawa Pharmaceuticals).
  14. ↑ "FK 482, a new orally active cephalosporin synthesis and biological properties". The Journal of Antibiotics 41 (6): 828–30. June 1988. doi:10.7164/antibiotics.41.828. PMID 3255303. 
  15. ↑ "Synthesis and biological activity of a new cephalosporin, BMY-28232 and its prodrug-type esters for oral use". The Journal of Antibiotics 41 (11): 1602–16. November 1988. doi:10.7164/antibiotics.41.1602. PMID 3198494. 
  16. ↑ "An alternative procedure for preparation of cefdinir". Farmaco 58 (6): 409–18. June 2003. doi:10.1016/S0014-827X(03)00063-6. PMID 12767379. 

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