青霉素
化学
普鲁卡因
分子
钾
青霉素耐药性
立体化学
抗生素
结晶学
生物化学
有机化学
生物
神经科学
作者
David D. Dexter,J. M. VAN DER VEEN
出处
期刊:Perkin Transactions
[The Royal Society of Chemistry]
日期:1978-01-01
卷期号:3 (3): 185-185
被引量:47
摘要
The geometric details and mode of puckering of the five-membered (thiazolidine) ring have been found to be different in two penicillin G salts. In procaine penicillin G monohydrate (aqueous procaine penicillin G or APPG) the penicillin molecule is in an 'extended' form whereas it is 'coiled' in potassium penicillin G. The solid-state conformation of penicillin G therefore depends more on local environment than on nature of substitution in the side chain. The procaine molecules in APPG adopt an enlarged (91°) torsion angle in the O–C–C–N group and exhibit little quinonoid character in the p-aminobenzoate group.
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