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???? ? >7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID
7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID
7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID ??
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189.2-191.0°
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D25 +366° (pyridine)
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648.4±55.0 °C(Predicted)
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1.43±0.1 g/cm3(Predicted)
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Hygroscopic, -20°C Freezer, Under inert atmosphere
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DMSO(??), ???(??), ???(??)? ???
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2.45±0.50(Predicted)
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Danger
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P- ??
H317
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P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H334
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P261, P285, P304+P341, P342+P311,P501
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P261
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P272
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P280
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P285
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P302+P352
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P304+P341
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P321
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P333+P313
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P342+P311
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P363
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P501
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7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID C??? ??, ??, ??
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Hetacillin was synthesized by Bristol-Myers
Laboratories in 1964. It shows activity as strong
as that of ampicillin against a variety of
gram-positive and gram-negative bacteria.
Hetacillin shows almost the same pharmacokinetic properties as ampicillin when administered
orally and a later serum peak when given by intramuscular administration. When administered
either orally or intramuscularly, it is hydrolyzed
in vivo into ampicillin. Therefore, the clinical
applications of hetacillin are the same as those
of ampicillin.
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Antibacterial.
7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID ?? ?? ? ???
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7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID ?? ??
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China 21
Germany 1
India 1
United Kingdom 1
United States 11
Global 35
7-(2,2-DIMETHYL-5-OXO-4-PHENYL-IMIDAZOLIDIN-1-YL)-3,3-DIMETHYL-6-OXO-2-THIA-5-AZABICYCLO[3.2.0]HEPTANE-4-CARBOXYLIC ACID ?? ??: