Heterocyclic Resveratrol Analogs: Synthesis and Physiological Activity. Part 2: Analogs Obtained by the Replacement of Ethylene Fragments with Heterocyclic Residues

[1]  Gheyath K Nasrallah,et al.  Potential Adverse Effects of Resveratrol: A Literature Review , 2020, International journal of molecular sciences.

[2]  G. Lizard,et al.  Aza- and Azo-Stilbenes: Bio-Isosteric Analogs of Resveratrol , 2020, Molecules.

[3]  P. Wlaź,et al.  Anticonvulsant Activity of Pterostilbene in Zebrafish and Mouse Acute Seizure Tests , 2019, Neurochemical Research.

[4]  P. Vicendo,et al.  Clearing up the photochemistry of resveratrol: Effect of the solvent , 2018, Journal of Photochemistry and Photobiology A: Chemistry.

[5]  R. Dellinger,et al.  Polyphenolic Phytochemicals in Cancer Prevention and Therapy: Bioavailability versus Bioefficacy. , 2017, Journal of medicinal chemistry.

[6]  Tsai-Teng Tzeng,et al.  Neuroprotective and Antineuroinflammatory Effects of Hydroxyl-Functionalized Stilbenes and 2-Arylbenzo[b]furans. , 2017, Journal of medicinal chemistry.

[7]  S. Chatterjee,et al.  Dominant Carbons in trans- and cis-Resveratrol Isomerization. , 2017, The journal of physical chemistry. B.

[8]  J. Palazón,et al.  Production of highly bioactive resveratrol analogues pterostilbene and piceatannol in metabolically engineered grapevine cell cultures , 2016, Plant biotechnology journal.

[9]  I. Mlinarič-Raščan,et al.  Antioxidant and anti-inflammatory properties of 1,2,4-oxadiazole analogs of resveratrol. , 2015, Chemico-biological interactions.

[10]  O. Ivashkevich,et al.  Deprotometalation-iodolysis and computed CH acidity of 1,2,3- and 1,2,4-triazoles. Application to the synthesis of resveratrol analogues. , 2015, Bioorganic & medicinal chemistry.

[11]  Špela Zupančič,et al.  Stability and solubility of trans-resveratrol are strongly influenced by pH and temperature. , 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[12]  Xingshu Li,et al.  Design, synthesis, and biological evaluation of benzoselenazole-stilbene hybrids as multi-target-directed anti-cancer agents. , 2015, European journal of medicinal chemistry.

[13]  F. Bellina,et al.  Imidazole analogues of resveratrol: synthesis and cancer cell growth evaluation , 2015 .

[14]  E. Novellino,et al.  Biological activity of 3-chloro-azetidin-2-one derivatives having interesting antiproliferative activity on human breast cancer cell lines. , 2013, Bioorganic & medicinal chemistry letters.

[15]  E. Novellino,et al.  Synthesis and cytotoxic activity evaluation of 2,3-thiazolidin-4-one derivatives on human breast cancer cell lines. , 2013, Bioorganic & medicinal chemistry letters.

[16]  J. Pezzuto,et al.  Optimization of thiazole analogues of resveratrol for induction of NAD(P)H:quinone reductase 1 (QR1). , 2012, Bioorganic & medicinal chemistry.

[17]  L. M. Mansky,et al.  Anti-HIV-1 activity of resveratrol derivatives and synergistic inhibition of HIV-1 by the combination of resveratrol and decitabine. , 2012, Bioorganic & medicinal chemistry letters.

[18]  B. Siewert,et al.  Synthesis and biological evaluation of novel (E) stilbene-based antitumor agents. , 2012, European journal of medicinal chemistry.

[19]  J. Pezzuto,et al.  Optimization of the aromatase inhibitory activities of pyridylthiazole analogues of resveratrol. , 2012, Bioorganic & medicinal chemistry.

[20]  Bo Zhou,et al.  Synthesis and biological evaluation of hydroxylated 3-phenylcoumarins as antioxidants and antiproliferative agents. , 2011, Bioorganic & medicinal chemistry letters.

[21]  T. Tuccinardi,et al.  Synthesis of heterocycle-based analogs of resveratrol and their antitumor and vasorelaxing properties. , 2010, Bioorganic & medicinal chemistry.

[22]  T. Mueller,et al.  4-(3-Halo/amino-4,5-dimethoxyphenyl)-5-aryloxazoles and -N-methylimidazoles that are cytotoxic against combretastatin A resistant tumor cells and vascular disrupting in a cisplatin resistant germ cell tumor model. , 2010, Journal of medicinal chemistry.

[23]  A. Brancale,et al.  Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cis-restricted combretastatin analogues. , 2010, Journal of medicinal chemistry.

[24]  M. Recanatini,et al.  Identification of a terphenyl derivative that blocks the cell cycle in the G0-G1 phase and induces differentiation in leukemia cells. , 2006, Journal of medicinal chemistry.

[25]  G. Tron,et al.  Rapid synthesis of triazole-modified resveratrol analogues via click chemistry. , 2006, Journal of medicinal chemistry.

[26]  G. Giannini,et al.  Heterocyclic and phenyl double-bond-locked combretastatin analogues possessing potent apoptosis-inducing activity in HL60 and in MDR cell lines. , 2005, Journal of medicinal chemistry.

[27]  R. Baruchello,et al.  Synthesis and biological evaluation of resveratrol and analogues as apoptosis-inducing agents. , 2003, Journal of medicinal chemistry.

[28]  J. Pezzuto,et al.  Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets. , 2012, Bioorganic & medicinal chemistry.