Paper Title
A BRIEF REVIEW ON SYNTHESIS AND BIOLOGICAL ACTIVITY OF RANOLAZINE
Article Identifiers
Authors
Miss.Isha Dnyandeo Gunjawate , Miss.Priti Kolpe , Miss.Jyoti Jawale , Miss.Ishwari Kale , Miss.Kranti Payghan
Keywords
Ranolazine, Synthesis, Anti-anginal, Biological activity, structure
Abstract
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.
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How To Cite
"A BRIEF REVIEW ON SYNTHESIS AND BIOLOGICAL ACTIVITY OF RANOLAZINE ", IJNRD - INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT (www.IJNRD.org), ISSN:2456-4184, Vol.8, Issue 10, page no.d622-d628, October-2023, Available :https://ijnrd.org/papers/IJNRD2310384.pdf
Issue
Volume 8 Issue 10, October-2023
Pages : d622-d628
Other Publication Details
Paper Reg. ID: IJNRD_207752
Published Paper Id: IJNRD2310384
Downloads: 000121233
Research Area: Pharmacy
Country: Pune, Maharashtra, India
Published Paper PDF: https://ijnrd.org/papers/IJNRD2310384.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2310384
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Journal Name: INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT(IJNRD)
ISSN: 2456-4184 | IMPACT FACTOR: 8.76 Calculated By Google Scholar | ESTD YEAR: 2016
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