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Cefatrizin

Cefatrizine Struktur
51627-14-6
CAS-Nr.
51627-14-6
Bezeichnung:
Cefatrizin
Englisch Name:
Cefatrizine
Synonyma:
CEFATRIZINE PROPYLENE GLYCOL;Cephathiamidine;s640p;bls640;eta(r)))-;SKF-60771;CEFATRIZINE;cephatriazine;antibioticbl-640;CEPHATHIAMIDINUM
CBNumber:
CB3116636
Summenformel:
C18H18N6O5S2
Molgewicht:
462.5
MOL-Datei:
51627-14-6.mol

Cefatrizin Eigenschaften

Siedepunkt:
948.1±65.0 °C(Predicted)
Dichte
1.3806 (rough estimate)
Brechungsindex
1.7000 (estimate)
storage temp. 
Store at -20°C
L?slichkeit
DMSO: 95 mg/mL (201.02 mM);Ethanol: 23 mg/mL (48.67 mM)
pka
2+-.0.50(Predicted)
Wasserl?slichkeit
Water: 95 mg/mL (201.02 mM)
CAS Datenbank
51627-14-6(CAS DataBase Reference)

Sicherheit

Toxizit?t LD50 in male, female mice, male, female rats (mg/kg): 6880, 6410, 4325, 4325 i.p. (Matsuzaki)

Cefatrizin Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Cefatrizine was synthesized by BristolMyers Co. and Smith Klein & French Laboratories in 1974. It shows two to four times higher activity against gram-positive and four to eight times higher activity against gram-negative bacteria than cephalexin. Cefatrizine also shows excellent oral absorption, and its in vivo activity is 30 to 500 times higher than that of cephalexin.

Verwenden

Cefatrizine is a new orally administered cephalosporin with excellent activity against gram-positive cocci, inhibiting all except enterococci at minimal inhibitory concentrations below 1 μg/ml.

Definition

ChEBI: A cephalosporin compound having (1H-1,2,3-triazol-4-ylsulfanyl)methyl and [(2R)-2-amino-2-(4-hydroxyphenyl)]acetamido side-groups. An antibacterial drug first prepared in the 1970s, it has more recently been found to be n inhibitor of eukaryotic elongation factor-2 kinase (eEF2K), which is known to regulate apoptosis, autophagy and ER stress in many types of human cancers.

Antimicrobial activity

A semisynthetic cephalosporin formulated for oral use. The spectrum is similar to that of cefalexin but it is more active against H. influenzae. Wide strain variations in susceptibility have been reported.
It is only partially absorbed when given by mouth. A 500 mg oral dose achieves a concentration of c. 6 mg/L after 1–2 h. The normal half-life of 2.5 h is extended to 5.5 h in end-stage renal failure. Distribution resembles that of cefalexin. It crosses the placenta readily. Plasma protein binding is 40–60%.
Urinary recovery in 6 h is 35% of an oral dose, producing urinary levels of 50–1500 mg/L. It is presumed that the remainder is metabolized, but no metabolites have been identified.
Apart from some mild diarrhea, it is well tolerated. It is available in Japan.

Sicherheitsprofil

Moderately toxic byintraperitoneal and subcutaneous routes. An experimentalteratogen. Other experimental reproductive effects. Whenheated to decomposition it emits very highly toxic fumesof NOx and SOx.

Cefatrizin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Cefatrizin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 112)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Xiamen AmoyChem Co., Ltd
+86-86-5926051114
sales@amoychem.com China 6361 58
CONIER CHEM AND PHARMA LIMITED

sales@conier.com China 49906 58
career henan chemical co
+86-0371-86658258
factory@coreychem.com China 29780 58
SIMAGCHEM CORP
+86-5922680277 +86-13806087780
sale@simagchem.com China 17339 58
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000
marketing@targetmol.com United States 32431 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +86-189 4982 3763
sales@tnjchem.com China 34526 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-17392587031
1059@dideu.com China 9984 58
Baoji Guokang Healthchem Co., Ltd.
+86-0917-3909592 +86-13892490616
gksales1@gk-bio.com China 9040 58
BOC Sciences
16314854226; +8616314854226
inquiry@bocsci.com United States 19852 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 17705817739
info@dycnchem.com China 52693 58

51627-14-6(Cefatrizin)Verwandte Suche:


  • CEFATRIZINE
  • 7-[2-(4-hydroxyphenyl)-2-aminoacetamido]-3-(1,2,3-triazole-4-ylthio)methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
  • antibioticbl-640
  • antibioticbl-s640
  • bls640
  • cephatriazine
  • eta(r)))-
  • l)acetyl)amino)-8-oxo-3-((1h-1,2,3-triazol-4-ylthio)methyl)-,(6r-(6-alpha,7-b
  • s640p
  • SKF-60771
  • CEFATRIZINE IMPURITY A7-AMINO-(6R,7R)-3-[(2H-1,2,3-TRIAZOL-4-YL)SULFANYL]-METHYL-8-OXO-5-THIA-1-AZABICYCLO[4.2.O]OCT-2-ENE-2-CARBOXYLIC ACID(7-ACA TRIAZOLE) EPC(CRM STANDARD)
  • CEPHATHIAMIDINUM
  • (6R,7R)-7-[[2-amino-2-(4-hydroxyphenyl)acetyl]amino]-8-oxo-3-(2H-triazol-4-ylsulfanylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2R)-2-aMino-2-(4-hydroxyphenyl)acetyl]aMino]-8-oxo-3-[(1H-1,2,3-triazol-5-ylthio)Methyl]-,(6R,7R)-
  • Cefatrizine USP/EP/BP
  • Cefathiamidine?(sterile)
  • CEFATRIZINE PROPYLENE GLYCOL
  • Cephathiamidine
  • 51627-14-6
  • 57627-40-2
  • 330175-00-2
  • C19H28N4O6S2
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