## Abstract The fungistatic activity of 127 benzene derivatives is reported and their behaviour related to structure and, in less detail, to solubility. The aromatic nucleus is more effective than its saturated counterpart. The effect of hydrophilic and nitro groups substituted in the benzene ring
Relationship between spatial structure and pharmacological activity of a series of β-adrenomimetics
✍ Scribed by B. S. Zhorov; V. A. Govyrin
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 455 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0020-7608
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✦ Synopsis
Abstract
All equilibrium conformations of a series of N‐alkyl‐α‐alkyl derivatives of noradrenaline and their synthetic precursors—phenylaminoketones—have been calculated. It has been shown that spasmodic changes in bronchodilating activity of the catecholamines, observed with the increase in α‐alkyl substituent size, may arise from the difference in the ratio of diastereoisomers produced by reduction of aminoketones.
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