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Natural Products Chemistry and Pharmacognosy Commons

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331 full-text articles. Page 16 of 16.

Pharmaceutical Crops: An Overview, Shiyou Li, Wei Yuan, Peiying Yang, Mikhail Antoun, Michael Balick, Gordon Cragg 2010 Stephen F Austin State University, Arthur Temple College of Forestry and Agriculture

Pharmaceutical Crops: An Overview, Shiyou Li, Wei Yuan, Peiying Yang, Mikhail Antoun, Michael Balick, Gordon Cragg

Faculty Publications

Pharmaceutical crops is an ambiguous term used by biologists and chemists for different categories of plants. We define pharmaceutical crops as those cultivated species that are used for extraction or preparation of therapeutic substances such as active pharmaceutical ingredients (APIs), excipients used in pharmaceutical formulations, vaccines and antibodies, as well as other therapeutic proteins. Based on the type of pharmaceutical product, these crops can be classified into three distinct yet sometimes overlapping categories: crops for the production of small therapeutic molecules (STMs), large therapeutic molecules (LMTs), or standard therapeutic extracts (STEs). This review briefly discusses the relationships of pharmaceutical crops ...


The Nonpsychoactive Cannabinoid Cannabidiol Inhibits 5-Hydroxytryptamine3a Receptor-Mediated Currents In Xenopus Laevis Oocytes, Keun-Hang Susan Yang, Sehamuddin Galadari, Dmytro Isaev, Georg Petroianu, Toni S. Shippenberg, Murat Oz 2010 Chapman University

The Nonpsychoactive Cannabinoid Cannabidiol Inhibits 5-Hydroxytryptamine3a Receptor-Mediated Currents In Xenopus Laevis Oocytes, Keun-Hang Susan Yang, Sehamuddin Galadari, Dmytro Isaev, Georg Petroianu, Toni S. Shippenberg, Murat Oz

Mathematics, Physics, and Computer Science Faculty Articles and Research

The effect of the plant-derived nonpsychotropic cannabinoid, cannabidiol (CBD), on the function of hydroxytryptamine (5-HT)3A receptors expressed in Xenopus laevis oocytes was investigated using two-electrode voltage-clamp techniques. CBD reversibly inhibited 5-HT (1 μM)-evoked currents in a concentration-dependent manner (IC50 = 0.6 μM). CBD (1 μM) did not alter specific binding of the 5-HT3A antagonist [3H]3-(5-methyl-1H-imidazol-4-yl)-1-(1-methylindol-3-yl)propan-1-one (GR65630), in oocytes expressing 5-HT3A receptors. In the presence of 1 μM CBD, the maximal 5-HT-induced currents were also inhibited. The EC50 values were 1.2 and 1.4 μM, in the absence and presence of CBD, indicating ...


Synthesis Of (±)-Nosyberkol (Isotuberculosinol, Revised Structure Of Edaxadiene) And (±)-Tuberculosinol, Nathan Maugel, Francis M. Mann, Matthew L. Hillwig, Reuben J. Peters, Barry B. Snider 2010 Brandeis University

Synthesis Of (±)-Nosyberkol (Isotuberculosinol, Revised Structure Of Edaxadiene) And (±)-Tuberculosinol, Nathan Maugel, Francis M. Mann, Matthew L. Hillwig, Reuben J. Peters, Barry B. Snider

Biochemistry, Biophysics and Molecular Biology Publications

Me2AlCl-catalyzed Diels-Alder reaction of N-tigloyloxazolidinone with 6,6-dimethyl-1-vinylcyclohexene selectively provided the exo adduct, which was converted to nosyberkol (isotuberculosinol) and tuberculosinol. The spectral data for nosyberkol are identical with those reported for edaxadiene, whose structure is revised accordingly.


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