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Wikipedia

Ceftezole

Ceftezole (or ceftezol) is a semisynthetic first-generation cephalosporin antibiotic.[1]

Ceftezole
Clinical data
ATC code
Identifiers
  • (6R,7R)-8-oxo-7-{[2-(tetrazol-1-yl)acetyl]amino}-
    3-(1,3,4-thiadiazol-2-ylsulfanylmethyl)-5-thia-
    1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS Number
  • 26973-24-0
PubChem CID
  • 65755
ChemSpider
  • 59178 Y
UNII
  • 2Z86SYP11W
KEGG
  • D07656 Y
ChEMBL
  • ChEMBL1697829
CompTox Dashboard (EPA)
  • DTXSID0022771
ECHA InfoCard100.113.941
Chemical and physical data
FormulaC13H12N8O4S3
Molar mass440.47 g·mol−1
3D model (JSmol)
  • Interactive image
  • O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)Cn3nnnc3)CSc4nncs4)C(=O)O
  • InChI=1S/C13H12N8O4S3/c22-7(1-20-4-14-18-19-20)16-8-10(23)21-9(12(24)25)6(2-26-11(8)21)3-27-13-17-15-5-28-13/h4-5,8,11H,1-3H2,(H,16,22)(H,24,25)/t8-,11-/m1/s1 Y
  • Key:DZMVCVMFETWNIU-LDYMZIIASA-N Y

Ceftezole binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis.[citation needed]

Ceftezole is having (1,3,4-thiadiazol-2-ylsulfanyl)methyl and [2-(1H-tetrazol-1-yl)acetamido side groups located at positions 3 and 7 respectively. It is a cephalosporin and a member of thiadiazoles.[citation needed]

References edit

  1. ^ Berger SA (2021). "Ceftezole". GIDEON Guide to Antimicrobial Agents. Los Angeles: Gideon Informatics, Incorporated. p. 301. ISBN 978-1-4988-2958-8.

Note edit

  •   This article incorporates public domain material from Ceftezole (compound). National Center for Biotechnology Information - the National Library of Medicine - PubChem®.

External links edit

  •   Media related to Ceftezole at Wikimedia Commons


ceftezole, ceftezol, semisynthetic, first, generation, cephalosporin, antibiotic, clinical, dataatc, codej01db12, identifiersiupac, name, tetrazol, acetyl, amino, thiadiazol, ylsulfanylmethyl, thia, azabicyclo, carboxylic, acidcas, number26973, 0pubchem, cid65. Ceftezole or ceftezol is a semisynthetic first generation cephalosporin antibiotic 1 CeftezoleClinical dataATC codeJ01DB12 WHO IdentifiersIUPAC name 6R 7R 8 oxo 7 2 tetrazol 1 yl acetyl amino 3 1 3 4 thiadiazol 2 ylsulfanylmethyl 5 thia 1 azabicyclo 4 2 0 oct 2 ene 2 carboxylic acidCAS Number26973 24 0PubChem CID65755ChemSpider59178 YUNII2Z86SYP11WKEGGD07656 YChEMBLChEMBL1697829CompTox Dashboard EPA DTXSID0022771ECHA InfoCard100 113 941Chemical and physical dataFormulaC 13H 12N 8O 4S 3Molar mass440 47 g mol 13D model JSmol Interactive imageSMILES O C2N1 C C CS C H 1 C H 2NC O Cn3nnnc3 CSc4nncs4 C O OInChI InChI 1S C13H12N8O4S3 c22 7 1 20 4 14 18 19 20 16 8 10 23 21 9 12 24 25 6 2 26 11 8 21 3 27 13 17 15 5 28 13 h4 5 8 11H 1 3H2 H 16 22 H 24 25 t8 11 m1 s1 YKey DZMVCVMFETWNIU LDYMZIIASA N YCeftezole binds to and inactivates penicillin binding proteins PBPs located on the inner membrane of the bacterial cell wall PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division Inactivation of PBPs interferes with the cross linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity This results in the weakening of the bacterial cell wall and causes cell lysis citation needed Ceftezole is having 1 3 4 thiadiazol 2 ylsulfanyl methyl and 2 1H tetrazol 1 yl acetamido side groups located at positions 3 and 7 respectively It is a cephalosporin and a member of thiadiazoles citation needed References edit Berger SA 2021 Ceftezole GIDEON Guide to Antimicrobial Agents Los Angeles Gideon Informatics Incorporated p 301 ISBN 978 1 4988 2958 8 Note edit nbsp This article incorporates public domain material from Ceftezole compound National Center for Biotechnology Information the National Library of Medicine PubChem External links edit nbsp Media related to Ceftezole at Wikimedia Commons nbsp This systemic antibiotic related article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Ceftezole amp oldid 1167644595, wikipedia, wiki, book, books, library,

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