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Sutezolid

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Chemical compound

Pharmaceutical compound
Sutezolid
Clinical data
Other namesPNU-100480, PF-02341272
Identifiers
IUPAC name
  • N-methyl]acetamide
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.237.103 Edit this at Wikidata
Chemical and physical data
FormulaC16H20FN3O3S
Molar mass353.41 g·mol
3D model (JSmol)
SMILES
  • CC(=O)NC1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCSCC3)F
InChI
  • InChI=InChI=1S/C16H20FN3O3S/c1-11(21)18-9-13-10-20(16(22)23-13)12-2-3-15(14(17)8-12)19-4-6-24-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1
  • Key:FNDDDNOJWPQCBZ-ZDUSSCGKSA-N

Sutezolid is an investigational new drug that is being evaluated for the treatment of extensively drug-resistant tuberculosis. It differs from linezolid by replacement of the morpholine oxygen with a sulfur atom. Like linezolid, sutezolid is a bacterial protein synthesis inhibitor. In preclinical studies, sutezolid demonstrated superior antituberculosis activity compared to linezolid.

References

  1. "Sutezolid - Global Alliance for TB Drug Development/Sequella". AdisInsight. Springer Nature Switzerland AG.
  2. Chen RH, Burke A, Cho JG, Alffenaar JW, Davies Forsman L (June 2024). "New Oxazolidinones for Tuberculosis: Are Novel Treatments on the Horizon?". Pharmaceutics. 16 (6): 818. doi:10.3390/pharmaceutics16060818. PMC 11207443. PMID 38931939.
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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