INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT International Peer Reviewed & Refereed Journals, Open Access Journal ISSN Approved Journal No: 2456-4184 | Impact factor: 8.76 | ESTD Year: 2016
Scholarly open access journals, Peer-reviewed, and Refereed Journals, Impact factor 8.76 (Calculate by google scholar and Semantic Scholar | AI-Powered Research Tool) , Multidisciplinary, Monthly, Indexing in all major database & Metadata, Citation Generator, Digital Object Identifier(DOI)
Currently approved as a second-line treatment for chronic stable angina pectoris in both the US and Europe, ranolazine is a derivative of Piperazine. Chemically defined as N(6,2dimethylphenyl)-2-(4-2-hydroxy-3-(2-methoxyphenoxy)propyl)piperazin-1-yl)acetamide, ranolazine is a racemic combination. Ranolazine belongs to a group of drugs known as anti-angina drugs. Usually, this medication is taken in combination with other medications. It can be taken either on its alone or in combination with calcium channel blockers, beta-blockers, angiotensin receptor blockers, anti-platelet medications, and nitrates. Many medicinal chemists are interested in investigating the entity's diverse pharmacological and biological potentials. Because of its strong biological action, ranolazine is a key component in medicinal chemistry. The synthetic process utilised to prepare ranolazine last year is revised in this article and has demonstrated biological.
"A BRIEF REVIEW ON SYNTHESIS AND BIOLOGICAL ACTIVITY OF RANOLAZINE ", International Journal of Novel Research and Development (www.ijnrd.org), ISSN:2456-4184, Vol.8, Issue 10, page no.d622-d628, October-2023, Available :http://www.ijnrd.org/papers/IJNRD2310384.pdf
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2456-4184 | IMPACT FACTOR: 8.76 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.76 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator
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