Name | azlocillin |
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Synonyms |
(2S,5R,6R)-3,3-Dimethyl-7-oxo-6-{[(2R)-2-{[(2-oxo-1-imidazolidinyl)carbonyl]amino}-2-phenylacetyl]amino}-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Azlocillin 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[[(2R)-2-[[(2-oxo-1-imidazolidinyl)carbonyl]amino]-2-phenylacetyl]amino]-, (2S,5R,6R)- (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-((R)-2-(2-oxo-1-imidazolidinecarboxamido)-2-phenylacetamido)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid |
Description | Azlocillin, an antibiotic, is a semisynthetic penicillin, and has broad-spectrum antibacterial activity. Azlocillin is active against drug-tolerant B. burgdorferi sensu stricto JLB31 infection[1][2]. |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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Molecular Formula | C20H23N5O6S |
Molecular Weight | 461.491 |
Exact Mass | 461.136902 |
PSA | 173.45000 |
LogP | -0.34 |
Index of Refraction | 1.697 |
~89% 37091-66-0 |
Literature: Koenig, Hans-Bodo; Metzer, Karl-Georg; Offe, Hans-Albert; Schroeck, Wilfried European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 59 - 63 |
~% 37091-66-0 |
Literature: Koenig, Hans-Bodo; Metzer, Karl-Georg; Offe, Hans-Albert; Schroeck, Wilfried European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 59 - 63 |
Precursor 4 | |
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DownStream 0 |