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CasNo: 62893-20-3
Molecular Formula: C25H27N9O8S2. Na
Appearance: Faint beige powder
Therapeutic Function |
Antibiotic |
Biological Activity |
cefoperazone is a new semisynthetic cephalosporin with a broad spectrum of antibacterial activity. cefoperazone shows high activity against gram-positive bacteria and gram-negative bacilli, such as escherichia coli, klebsiella pneumoniae, and proteus species [1]. |
Veterinary Drugs and Treatments |
Cefoperazone is used to treat serious infections, particularly susceptible Enterobacteriaceae not susceptible to other less expensive agents or when aminoglycosides are not indicated (due to their potential toxicity). |
in vitro |
there was only a small spread between the minimum inhibitory concentrations and the minimum bactericidal concentrations of cefoperazone and a significant decrease in activity with an increase in inoculum size. cefoperazone is relatively stable to hydrolysis to β-lactamases produced by gram-negative bacteria. relative rates of hydrolysis of cefoperazone by cephalosporinases were 7.0 to 0.01[1]. in 50 strains of n. gonorrhoeae, the mic50 of cefoperazone was ≤ 0.004-0.06 μg/ml [2]. |
in vivo |
in four patients with cholelithiasis and one patient with carcinoma of the head of the pancreas, all of whom had normal renal functions, cefoperazone was intravenously administrated. in common duct bile, the maximum concentrations of cefoperazone ranged from 373.4 to 3,100 μg/ml while the concentrations ranged from 6.8 to 680 μg/ml in gall bladder bile. cefoperazone concentrations of the gall bladder wall ranged from 16.8 to 48.0 μg/g [3]. |
references |
[1] matsubara n, minami s, muraoka t, et al. in vitro antibacterial activity of cefoperazone (t-1551), a new semisynthetic cephalosporin[j]. antimicrobial agents and chemotherapy, 1979, 16(6): 731-735.[2] baker c n, thornsberry c, jones r n. in vitro antimicrobial activity of cefoperazone, cefotaxime, moxalactam (ly127935), azlocillin, mezlocillin, and other beta-lactam antibiotics against neisseria gonorrhoeae and haemophilus influenzae, including beta-lactamase-producing strains[j]. antimicrobial agents and chemotherapy, 1980, 17(4): 757-761.[3] nakamura t, hashimoto i, sawada y, et al. cefoperazone concentrations in bile and gall bladder wall after intravenous administration[j]. antimicrobial agents and chemotherapy, 1980, 18(6): 980-982. |
InChI:InChI=1/C25H27N9O8S2.Na/c1-3-32-8-9-33(21(39)20(32)38)24(42)27-15(12-4-6-14(35)7-5-12)18(36)26-16-19(37)34-17(23(40)41)13(10-43-22(16)34)11-44-25-28-29-30-31(25)2;/h4-7,15-16,22,35H,3,8-11H2,1-2H3,(H,26,36)(H,27,42)(H,40,41);/q;+1/p-1/t15-,16-,22-;/m1./s1
The invention discloses new adaptation d...
The invention discloses a cefoperazone s...
The invention discloses a cefoperazone s...
The present invention relates to a new c...
cefoperazone
Cefobis
Conditions | Yield |
---|---|
With
sodium hydrogencarbonate;
In
water; acetone;
at 15 - 25 ℃;
for 0.666667h;
pH=6.5 - 6.6;
|
98.1% |
With
sodium isooctanoate; pyrographite;
In
acetone;
at 25 ℃;
pH=6.6;
Reagent/catalyst;
pH-value;
|
71.8% |
With
sodium carbonate;
In
water; ethyl acetate;
at 25 ℃;
pH=6.2;
Temperature;
Solvent;
pH-value;
|
102.61 g |
With
sodium hydrogencarbonate;
In
ethanol; water;
at 30 ℃;
pH=6;
Reagent/catalyst;
Solvent;
Temperature;
pH-value;
|
453g |
7-Aminocephalosporanic acid
Cefobis
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps
1: pyridine; titanium tetrachloride; tetrabutoxytitanium / acetonitrile / 3 h / 5 - 30 °C
2: chloro-trimethyl-silane / N,N-dimethyl-formamide / 4 h / -25 - -20 °C
3: sodium isooctanoate; pyrographite / acetone / 25 °C / pH 6.6
With
pyridine; tetrabutoxytitanium; chloro-trimethyl-silane; sodium isooctanoate; titanium tetrachloride; pyrographite;
In
N,N-dimethyl-formamide; acetone; acetonitrile;
|
cefoperazone
7-Aminocephalosporanic acid
C25H26N9O8S2(1-)*Fe(2+)*Cl(1-)
C25H26N9O8S2(1-)*Cd(2+)*Cl(1-)