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John M. Pezzuto

Researcher at Long Island University

Publications -  599
Citations -  38474

John M. Pezzuto is an academic researcher from Long Island University. The author has contributed to research in topics: Cancer & Resveratrol. The author has an hindex of 88, co-authored 588 publications receiving 35901 citations. Previous affiliations of John M. Pezzuto include Purdue University & Bandung Institute of Technology.

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Nigranoic acid, a triterpenoid from Schisandra sphaerandra that inhibits HIV-1 reverse transcriptase

TL;DR: Nigranoic acid showed activity in several anti-HIV reverse transcriptase and polymerase assays and its structure elucidation and unambiguous NMR spectral assignment were achieved by the combination of 1D- and 2D-NMR techniques with the aid of computer modeling.
PatentDOI

Aromatase inhibitors from Broussonetia papyrifera

TL;DR: In this article, a composition and method of cancer treatment using B. papyrifera extract and compounds having aromatase inhibition properties was presented. But the method was not described.
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Resveratrol inhibits phorbol ester and UV-induced activator protein 1 activation by interfering with mitogen-activated protein kinase pathways.

TL;DR: The results suggest that the effects of resveratrol on AP-1 and MAPK pathways may involve the inhibition of both protein tyrosine kinases and protein kinase C.
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Inhibition of aromatase activity by flavonoids.

TL;DR: In searching for potent cancer chemopreventive agents from synthetic or natural products, 28 randomly selected flavonoids were screened for inhibitory effects against partially purified aromatase prepared from human placenta, with greatest activity being demonstrated with apigenin,rysin, and hesperetin.
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Potential anti-inflammatory phenolic glycosides from the medicinal plant Moringa oleifera fruits

TL;DR: Bioassay-guided isolation and purification of the ethyl acetate extract of Moringa oleifera fruits yielded three new phenolic glycosides that are reported to have potent NO-inhibitory activity and reduced LPS-mediated iNOS expression.