Synthesis and biological activity of (theobromine-1-yl)acetic acid benzyliden hydrazides

dc.contributor.authorIvanchenko, D. G.
dc.contributor.authorVarahabhatla, S. C. R. V.
dc.contributor.authorІванченко, Дмитро Григорович
dc.date.accessioned2018-12-21T08:42:30Z
dc.date.available2018-12-21T08:42:30Z
dc.date.issued2015
dc.description.abstractKey way for creating new medicinal drugs is structural modification of known and existent natural compounds with high biological activity. In this aspect researchers’ attention is drawn by xanthine derivatives which appear to be antagonists of adenosine receptors, phosphodiesterase inhibitors and histone deacetylase inducers. This resulted in their widespread application in medicine as diuretics, analgesics, heart pacemakers, anti-inflammatory, psychotropic and renal protective agents.uk_UK
dc.identifier.citationIvanchenko D. G. Synthesis and biological activity of (theobromine-1-yl)acetic acid benzyliden hydrazides / D. G. Ivanchenko, S. C. R. V. Varahabhatla; scientific supervisor: Dr., prof. Romanenko M. I. // Сучасні аспекти медицини і фармації – 2015 : тези доп. Всеукр. наук.-практ. конф. молодих вчених та студентів з міжнар. участю, присвяч. Дню науки, 14-15 трав. 2015 р. – Запоріжжя, 2015. – С. 169.uk_UK
dc.identifier.urihttps://zsmu.rosbai.com/handle/123456789/8874
dc.language.isoenuk_UK
dc.publisherЗапорізький державний медичний університетuk_UK
dc.subjectтезиuk_UK
dc.titleSynthesis and biological activity of (theobromine-1-yl)acetic acid benzyliden hydrazidesuk_UK
dc.typeOtheruk_UK

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