Neurotropic and antitumor activities of silyl- and germyl-isoxazolin-2-yl derivatives
โ Scribed by E. Lukevics; P. Arsenyan; S. Germane; I. Shestakova
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 37 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0268-2605
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โฆ Synopsis
Neurotropic and antitumor activities of the pyridyl-substituted 5-Si(Ge)-isoxazolines and (3alkyl-4-triphenylgermylisoxazolin-2-yl)-5-carboxylic acid ethyl esters have been investigated. It has been shown that silylisoxazolin-2-yl derivatives are more potent in protection against hypoxia and Corazole convulsions than their analogues. Germylisoxazolin-2-yl compounds are stronger tumor growth inhibitors and NOinducers than their silyl analogues.
๐ SIMILAR VOLUMES
Symmetrically 4,16-disubstituted (3a-c) and bridged (6a, b) bis(trimethylsilyl)[2.2]paracyclophane (3a) we also examined the Grignard reaction, and as a result the first successful use organometallic paracyclophane derivatives have been synthesized for use as monomeric precursors of or-of a 4,16-bis
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