Grepafloxacin (trade name Raxar, Glaxo Wellcome) was an oral broad-spectrum fluoroquinolone antibacterial agent used to treat bacterial infections. Grepafloxacin was withdrawn worldwide from markets in 1999,[1][2] due to the drug's potential to cause a potentially fatal cardiac arrhythmia.[3]
 | |
| Clinical data | |
|---|---|
| AHFS/Drugs.com | Multum Consumer Information |
| ATC code | |
| Pharmacokinetic data | |
| Protein binding | 50% |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.159.692 |
| Chemical and physical data | |
| Formula | C19H22FN3O3 |
| Molar mass | 359.401 g·mol−1 |
| 3D model (JSmol) | |
| Chirality | Racemic mixture |
| |
| |
| (verify) | |
Clinical uses
editGrepafloxacin was used for treating exacerbations of chronic bronchitis caused by susceptible bacteria (e.g. Haemophilus influenzae, Streptococcus pneumoniae, Moraxella catarrhalis),[4][5][6] community-acquired pneumonia (including those, in addition to the above germs, caused by Mycoplasma pneumoniae)[7][8] gonorrhea and non-gonococcal urethritis and cervicitis (for example caused by Chlamydia trachomatis or Ureaplasma urealyticum).[9][10]
Synthesis
editThe preparation of quinolones bearing a substituent at position 5 is complicated by the greater electrophilic character of the 8 position. One scheme for resolving the problem consists in blocking access to position 8 by first adding a readily removable group to that center.
The scheme starts with the conversion of the carboxylic acid in (1) to its dimethyloxazoline derivative (3) by reaction with the aminomethyl propanol (2). Lithium diisopropylamide (LDA) then removes a proton from the 8 position; treatment of that anion with trimethylsilyl iodide leads to the silylated intermediate (4). A second round of LDA then generates a carbanion at the only open position; reaction with methyl iodide leads to the corresponding 5 methyl derivative (5). Treatment of that product with cesium fluoride breaks the carbon–silicon bond, removing the silyl group; aqueous acid then hydrolyzes the oxazoline to afford the free acid (6). This last intermediate is then taken on to the quinolone (9) [13] by essentially the same scheme as that used to prepare difloxacin, with the difference that the chain elongation is by means of Grignard reagent of ethyl bromoacetate. Treatment of (9) with 2-methylpiperazine proceeds by reaction at the less hindered of the two amino groups; saponification then affords grepafloxacin (10).
Stereochemistry
editGrepafloxacin contains a stereocenter and consists of two enantiomers. This is a racemate, ie a 1: 1 mixture of (R)- and the (S)-forms:
| Enantiomers of grepafloxacin | |
|---|---|
-Grepafloxacin_Structural_Formula_V1.svg) (R)-grepafloxacin CAS number: 146761-68-4 |
-Grepafloxacin_Structural_Formula_V1.svg) (S)-grepafloxacin CAS number: 146761-69-5 |
See also
editReferences
edit- ^ "Glaxo Wellcome voluntary withdrawn Raxar (Grepafloxacin)" (PDF). Food and Drug Administration. Retrieved 2014-10-12.
- ^ "Withdrawal of Product: RAXAR (grepafloxacin HCl) 600 mg Tablets, 400 mg Tablets, and 200 mg Tablets". U.S. Food and Drug Administration. Retrieved 2014-10-12.
- ^ Sprandel KA, Rodvold KA (2003). "Safety and tolerability of fluoroquinolones". Clinical Cornerstone. Suppl 3: S29–S36. doi:10.1016/s1098-3597(03)90027-5. PMID 14992418.
- ^ Chodosh S, Lakshminarayan S, Swarz H, Breisch S (January 1998). "Efficacy and safety of a 10-day course of 400 or 600 milligrams of grepafloxacin once daily for treatment of acute bacterial exacerbations of chronic bronchitis: comparison with a 10-day course of 500 milligrams of ciprofloxacin twice daily". Antimicrobial Agents and Chemotherapy. 42 (1): 114–120. doi:10.1128/AAC.42.1.114. PMC 105465. PMID 9449270.
- ^ Langan CE, Cranfield R, Breisch S, Pettit R (December 1997). "Randomized, double-blind study of grepafloxacin versus amoxycillin in patients with acute bacterial exacerbations of chronic bronchitis". The Journal of Antimicrobial Chemotherapy. 40 Suppl A: 63–72. doi:10.1093/jac/40.suppl_1.63. PMID 9484875.
- ^ Langan CE, Zuck P, Vogel F, McIvor A, Peirzchala W, Smakal M, et al. (October 1999). "Randomized, double-blind study of short-course (5 day) grepafloxacin versus 10 day clarithromycin in patients with acute bacterial exacerbations of chronic bronchitis". The Journal of Antimicrobial Chemotherapy. 44 (4): 515–523. doi:10.1093/jac/44.4.515. PMID 10588313.
- ^ O'Doherty B, Dutchman DA, Pettit R, Maroli A (December 1997). "Randomized, double-blind, comparative study of grepafloxacin and amoxycillin in the treatment of patients with community-acquired pneumonia". The Journal of Antimicrobial Chemotherapy. 40 Suppl A: 73–81. doi:10.1093/jac/40.suppl_1.73. PMID 9484876.
- ^ Felmingham D (March 2000). "Respiratory pathogens: assessing resistance patterns in Europe and the potential role of grepafloxacin as treatment of patients with infections caused by these organisms". The Journal of Antimicrobial Chemotherapy. 45 (90002): 1–8. doi:10.1093/jac/45.suppl_2.1. PMID 10719006.
- ^ Ridgway GL, Salman H, Robbins MJ, Dencer C, Felmingham D (December 1997). "The in-vitro activity of grepafloxacin against Chlamydia spp., Mycoplasma spp., Ureaplasma urealyticum and Legionella spp". The Journal of Antimicrobial Chemotherapy. 40 Suppl A: 31–34. doi:10.1093/jac/40.suppl_1.31. PMID 9484871.
- ^ McCormack WM, Martin DH, Hook EW, Jones RB (1998). "Daily oral grepafloxacin vs. twice daily oral doxycycline in the treatment of Chlamydia trachomatis endocervical infection". Infectious Diseases in Obstetrics and Gynecology. 6 (3): 109–115. doi:10.1155/S1064744998000210. PMC 1784789. PMID 9785106.
- ^ Hagen SE, Domagala JM, Heifetz CL, Johnson J (March 1991). "Synthesis and biological activity of 5-alkyl-1,7,8-trisubstituted-6-fluoroquinoline-3-carboxylic acids". Journal of Medicinal Chemistry. 34 (3): 1155–1161. doi:10.1021/jm00107a040. PMID 2002456.
- ^ WO 8906649; eidem, U.S. patent 4,920,120 (1989, 1990 both to Warner-Lambert).
- ^ Hagen SE, Domagala JM (1990). "Synthesis of 5-methyl-4-oxo-quinolinecarboxylic acids". Journal of Heterocyclic Chemistry. 27 (6): 1609–1616. doi:10.1002/jhet.5570270616.