Cefazolin structure
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Common Name | Cefazolin | ||
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CAS Number | 25953-19-9 | Molecular Weight | 454.507 | |
Density | 2.0±0.1 g/cm3 | Boiling Point | N/A | |
Molecular Formula | C14H14N8O4S3 | Melting Point | 198-200ºC | |
MSDS | N/A | Flash Point | N/A |
Use of CefazolinCefazolin is an antibiotic used for the research of a number of anti-bacterial infections. Cefazolin can be used for the prophylaxis of surgical antimicrobial. Cefazolin has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD)[1]. |
Name | cefazolin |
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Synonym | More Synonyms |
Description | Cefazolin is an antibiotic used for the research of a number of anti-bacterial infections. Cefazolin can be used for the prophylaxis of surgical antimicrobial. Cefazolin has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD)[1]. |
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Related Catalog | |
Target |
Antibiotic[1] |
In Vitro | Cefazolin (50-300 μg/mL; 6 or 24 hours) has a direct anti-inflammatory effect on C8-B4 cells stimulated by LPS (1 μg/mL)[1]. Cell Viability Assay[1] Cell Line: Mouse C8-B4 microglial cells Concentration: 50, 100, 150, 200, 250, and 300 μg/mL Incubation Time: 6 or 24 hours Result: Inhibited proinflammatory cytokine production. Inhibited IL-6 production at 50 and 100 μg/mL. |
In Vivo | Cefazolin (300 mg/kg; injected intraperitoneally 1 h before surgery and then once per day for 5 days after surgery) can attenuate surgery-induced post-operative memory and learning impairment in mice. Cefazolin alone may induce cognitive dysfunction possibly by transient gut dysbiosis in mice without surgery[1]. Animal Model: Six- to 8-week-old CD-1 male mice (weighing 31-36 g) [1] Dosage: 300-500 mg/kg Administration: 10 mg in 0.1 mL was intraperitoneally injected 30 min before surgery and then once every day for 5 days. Result: Improved learning and memory after surgery and might impair learning and memory in mice without surgery. |
References |
Density | 2.0±0.1 g/cm3 |
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Melting Point | 198-200ºC |
Molecular Formula | C14H14N8O4S3 |
Molecular Weight | 454.507 |
Exact Mass | 454.029999 |
PSA | 234.93000 |
LogP | 1.13 |
Index of Refraction | 1.961 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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~76% Cefazolin CAS#:25953-19-9 |
Literature: WO2005/20904 A2, ; Page/Page column 19 ; |
~92% Cefazolin CAS#:25953-19-9 |
Literature: Tetrahedron, , vol. 41, # 22 p. 5133 - 5139 |
~70% Cefazolin CAS#:25953-19-9 |
Literature: Tetrahedron Letters, , vol. 38, # 26 p. 4693 - 4696 |
~78% Cefazolin CAS#:25953-19-9 |
Literature: Journal of Organic Chemistry, , vol. 62, # 26 p. 9099 - 9106 |
~% Cefazolin CAS#:25953-19-9 |
Literature: Tetrahedron Letters, , vol. 38, # 26 p. 4693 - 4696 |
~% Cefazolin CAS#:25953-19-9 |
Literature: Tetrahedron Letters, , vol. 38, # 26 p. 4693 - 4696 |
~% Cefazolin CAS#:25953-19-9 |
Literature: Journal of Organic Chemistry, , vol. 62, # 26 p. 9099 - 9106 |
~% Cefazolin CAS#:25953-19-9 |
Literature: Chemical and Pharmaceutical Bulletin, , vol. 44, # 3 p. 599 - 601 |
Precursor 9 | |
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DownStream 0 |
HS Code | 3004909090 |
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Isolation of Escherichia coli strains with AcrAB-TolC efflux pump-associated intermediate interpretation or resistance to fluoroquinolone, chloramphenicol and aminopenicillin from dogs admitted to a university veterinary hospital.
J. Vet. Med. Sci. 76(7) , 937-45, (2014) Understanding the prevalence of antimicrobial-resistance and the relationship between emergence of resistant bacteria and clinical treatment can facilitate design of effective treatment strategies. We... |
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Aspiration sclerotherapy combined with pasireotide to improve reduction of large symptomatic hepatic cysts (SCLEROCYST): study protocol for a randomized controlled trial.
Trials 16 , 82, (2015) Aspiration sclerotherapy is an effective therapeutic option for large symptomatic hepatic cysts. However, incomplete cyst reduction following aspiration sclerotherapy is frequently reported. Strong po... |
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Skeletal muscle and plasma concentrations of cefazolin during cardiac surgery in infants.
J. Thorac. Cardiovasc. Surg. 148(6) , 2634-41, (2014) To describe the pharmacokinetics and tissue disposition of prophylactic cefazolin into skeletal muscle in a pediatric population undergoing cardiac surgery.The subjects included 12 children, with a me... |
Cephazolin |
7-(1-(1H)-Tetrazolylacetamido)-3-[2-(5-methyl-1,3,4-thiadiazolyl)thiomethyl]-D3-cephem-4-carboxylic Acid |
Cephamezine |
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-7-[[2-(1H-tetrazol-1-yl)acetyl]amino]-, (6R,7R)- |
Cefazolinum |
Cefazolina |
Cephazoline |
5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-, (6R,7R)- |
(6R,7R)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-7-[[2-(tetrazol-1-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
Cefazoline |
(6R,7R)-3-{[(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
Cephazolidin |
Ancef |
MFCD00243010 |
EINECS 247-362-8 |
Cefazolin |
(6R)-3-(5-methyl-[1,3,4]thiadiazol-2-ylsulfanylmethyl)-8-oxo-7t-(2-tetrazol-1-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
(6R,7R)-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl}-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
Cefamezin |
Cefazolin Acid |