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Cefotiam

Cefotiam ??? ???
?? ??:
61622-34-2
???:
Cefotiam
???(??):
SCE 963;Texodil;CEFOTIAM;Taketiam;cgp14221e;Pansporin T;CEFOTIAM HCL;(6r-trans)--oxo;Cefotiam USP/EP/BP;Pansporin:Pansporine
CBNumber:
CB7367629
???:
C18H23N9O4S3
??? ??:
525.63
MOL ??:
61622-34-2.mol

Cefotiam ??

?? ?
843℃
??
1.80±0.1 g/cm3(Predicted)
RTECS ??
XI0366000
???
>110°(230°F)
?? ??
2-8°C
?? ?? (pKa)
2.57±0.50(Predicted)
???
??
CAS ??????
61622-34-2(CAS DataBase Reference)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
????(GHS): GHS hazard pictograms
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H317 ????? ?? ??? ??? ? ?? ?? ??? ?? ?? 1 ?? GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H334 ?? ? ????? ??, ?? ?? ?? ?? ?? ??? ? ?? ??? ??? ?? ?? 1 ?? GHS hazard pictograms P261, P285, P304+P341, P342+P311,P501
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P272 ??? ??? ??? ??? ???? ???.
P280 ????/???/???/?????? ?????.
P285 ??? ? ?? ?? ???? ??? ???? ?????
P302+P352 ??? ??? ??? ?? ????.
P304+P341 ???? ??,??? ??? ?? ??? ??? ??? ?? ??? ??? ???? ?? ??? ??? ??? ?
P321 (…) ??? ???.
P333+P313 ????? ?? ??? ???? ???? ??·??? ????.
P342+P311 ??? ??? ???? ????(??)? ??? ????.
P363 ?? ??? ??? ??? ?????.
P501 ...? ??? / ??? ?? ???.

Cefotiam C??? ??, ??, ??

??

Antibacterial

??

ChEBI: A cephalosporin with ({1-[2-(dimethylamino)ethyl]-1H-tetrazol-5-yl}sulfanyl)methyl and (2-amino-1,3-thiazol-4-yl)acetamido substituents at positions 3 and 7, respectively, of the cephem skeleton. A third generation beta-lactam cephalospo in antibiotic, it is active against a broad spectrum of both Gram positive and Gram negative bacteria.

Antimicrobial activity

A semisynthetic cephalosporin formulated as the dihydrochloride for injection and as a prodrug ester, cefotiam hexetil, for oral administration. Activity is similar to that of cefuroxime, but it is somewhat more active against a range of enterobacteria .
A 30-min intravenous infusion of the dihydrochloride produces a peak serum concentration of 35 mg/L; the corresponding concentration after a 1 g intramuscular dose is 17 mg/L. Oral absorption of the hexetil ester is around 65%. Food delays absorption of the ester. The plasma half-life is 0.6–1.1 h. Around 40% is bound to plasma protein. Urinary excretion is almost complete 4 h after the end of intravenous infusion, but only 50–67% is recovered unchanged; there is substantial non-renal elimination and some evidence of saturation of renal tubular excretion at doses above 2 g. In anuria the plasma elimination half-life rises to 13 h and plasma and renal clearances parallel creatinine clearance. A small amount is excreted in bile. In patients with cholelithiasis given 0.5 or 1 g intravenously, mean concentrations in gallbladder bile and gallbladder wall 30 min after the dose were around 17 and 32 mg/L, respectively. In patients with normal liver function, hepatic bile concentrations can exceed 1 g/L.
It is generally well tolerated and has been used successfully to treat lower respiratory infections, skin and soft-tissue infection. It is not widely used, but is available in Japan and some other countries.

Cefotiam ?? ?? ? ???

???

?? ??


Cefotiam ?? ??

???( 96)?? ??
??? ?? ??? ?? ?? ? ??
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Cefotiam ?? ??:

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