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Eperezolid

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Chemical compound Pharmaceutical compound
Eperezolid
Skeletal formula of eperezolid
Space-filling model of the eperezolid molecule
Clinical data
ATC code
  • none
Identifiers
IUPAC name
  • (S)-N-phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC18H23FN4O5
Molar mass394.403 gยทmol
3D model (JSmol)
SMILES
  • CC(=O)NC1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCN(CC3)C(=O)CO)F
InChI
  • InChI=1S/C18H23FN4O5/c1-12(25)20-9-14-10-23(18(27)28-14)13-2-3-16(15(19)8-13)21-4-6-22(7-5-21)17(26)11-24/h2-3,8,14,24H,4-7,9-11H2,1H3,(H,20,25)/t14-/m0/s1
  • Key:SIMWTRCFFSTNMG-AWEZNQCLSA-N
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Eperezolid is an oxazolidinone antibiotic.

Synthesis

Eperezolid synthesis

See also

References

  1. Brickner SJ, Hutchinson DK, Barbachyn MR, Manninen PR, Ulanowicz DA, Garmon SA, et al. (February 1996). "Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant gram-positive bacterial infections". Journal of Medicinal Chemistry. 39 (3): 673โ€“9. doi:10.1021/jm9509556. PMID 8576909.
Antibacterials that inhibit protein synthesis (J01A, J01B, J01F, J01G, QJ01XQ)
30S
Aminoglycosides
(initiation inhibitors)
-mycin (Streptomyces)
-micin (Micromonospora)
other
Tetracycline antibiotics
(tRNA binding)
Tetracyclines
Glycylcyclines
50S
Oxazolidinone
(initiation inhibitors)
Peptidyl transferase
Amphenicols
MLS (transpeptidation/translocation)
Macrolides
Ketolides
Lincosamides
Streptogramins
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