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Journal ArticleDOI

Antiviral Activity of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol and its Derivatives Against Influenza A(H1N1)2009 Virus

TLDR
A number of new derivatives of monoterpenoid with a para-menthane framework 3-methyl-6-(prop-1-en-2- yl)cyclohex-3-ene-1,2-diol (-)-3 were synthesized and the absolute configuration of compound 6 was shown to be critical for its antiviral activity.
Abstract
A number of new derivatives of monoterpenoid with a para-menthane framework 3-methyl-6-(prop-1-en-2- yl)cyclohex-3-ene-1,2-diol (-)-3 were synthesized. The antiviral activity of (-)-3 and its derivatives against the pandemic influenza virus A/California/07/09 (H1N1)v was studied in vitro. Compound (-)-3 was found to be active against this vi- rus (selectivity index 7.5); for mononicotinate (+)-6 the selectivity index was 17. The absolute configuration of compound 6 was shown to be critical for its antiviral activity.

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Citations
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Journal ArticleDOI

Discovery of a new class of antiviral compounds: camphor imine derivatives.

TL;DR: A new class of compounds featuring a camphor moiety that exhibits potent inhibitory activity against influenza A (H1N1)pdm09 and A(H5N1), and the most potent antiviral compound is imine 2 with therapeutic index more than 500.
Journal ArticleDOI

Monoterpenes as a renewable source of biologically active compounds

TL;DR: In this article, a review of various types of biological activity exhibited by monoterpenes and their derivatives, including analgesic, anti-inflammatory, anticonvulsant, antidepressant and anti-Alzheimer, antiParkinsonian, antiviral, and antibacterial (anti-tuberculosis) effects is presented.
Journal ArticleDOI

Highly Potent Activity of (1R,2R,6S)-3-Methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in Animal Models of Parkinson’s Disease

TL;DR: The use of compound 1 resulted in nearly full recovery of the locomotor and exploratory activities and was as effective as the comparator agent (levodopa) in both MPTP and haloperidol animal models.
Journal ArticleDOI

Camphor-based symmetric diimines as inhibitors of influenza virus reproduction

TL;DR: Derivatives of camphor can be considered as prospective antiinfluenza compounds active against influenza viruses resistant to adamantane-based drugs.
Journal ArticleDOI

Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes

TL;DR: Just compound 5i that contains a fluorine substituent exhibited more potent anti-influenza activity along with low cytotoxicity, and two new promising types of antiviral compounds were identified.
References
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Journal ArticleDOI

Novel antiviral agents: a medicinal plant perspective

TL;DR: There are innumerable potentially useful medicinal plants and herbs waiting to be evaluated and exploited for therapeutic applications against genetically and functionally diverse viruses families such as Retroviridae, Hepadnaviridae and Herpesviridae.
Journal ArticleDOI

Chemical and biological evaluation of the essential oils of different Melaleuca species.

TL;DR: The essential oil of M. armillaris exhibited a marked antioxidant effect, it improved vitamin E, vitamin C and superoxide dismutase parameters so it can be used as a free radical suppressor in carbon tetrachloride treated animals.
Book ChapterDOI

Bioactivity of Essential Oils and Their Components

TL;DR: It is demonstrated that EOs and their components have many functional properties and exert their action in mammals as well as in other organisms (insects, fungi, bacteria and viruses) and the synergistic effect of EO components is a promising field that could lead to the optimisation of a given bioactivity.
Journal ArticleDOI

Reactions of Allyl Alcohols of the Pinane Series and of Their Epoxides in the Presence of Montmorillonite Clay

TL;DR: In this paper, the reactivity of allyl alcohols of the pinane series and of their epoxides in the presence of montmorillonite clay in intra-and intermolecular reactions was studied.
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