Synthesis and biological evaluation of a gamma-cyclodextrin-based formulation of the anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet). (Q39676137)

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scientific article published on 4 June 2010

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English	Synthesis and biological evaluation of a gamma-cyclodextrin-based formulation of the anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet).	scientific article published on 4 June 2010

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8 February 2020

Synthesis and biological evaluation of a gamma-cyclodextrin-based formulation of the anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet) (English)

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8 February 2020

Simone Lucarini

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8 February 2020

Giuseppe Diamantini

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Alessandra Fraternale

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8 February 2020

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Francesca Antonietti

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Maria Filomena Paoletti

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Andrea Tontini

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Mauro Magnani

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Andrea Duranti

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4 June 2010

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8 February 2020

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4085-4093

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8 February 2020

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Creative Commons Attribution 4.0 International

4 June 2010

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Structure elucidation of acid reaction products of indole-3-carbinol: detection in vivo and enzyme induction in vitro

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A potent indole-3-carbinol derived antitumor agent with pleiotropic effects on multiple signaling pathways in prostate cancer cells.

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The major cyclic trimeric product of indole-3-carbinol is a strong agonist of the estrogen receptor signaling pathway

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Indole-3-carbinol as a chemopreventive and anti-cancer agent

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A new class of peroxisome proliferator-activated receptor gamma (PPARgamma) agonists that inhibit growth of breast cancer cells: 1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes.

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12 December 2020

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Activation of Nur77 by selected 1,1-Bis(3'-indolyl)-1-(p-substituted phenyl)methanes induces apoptosis through nuclear pathways

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https://pubmed.ncbi.nlm.nih.gov/20657428

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Enhancement of chemically-induced HL-60 cell differentiation by 3,3'-diindolylmethane derivatives

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https://pubmed.ncbi.nlm.nih.gov/20657428

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Aromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: comparisons with 2,3,7,8-tetrachlorodibenzo-p-dioxin

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https://pubmed.ncbi.nlm.nih.gov/20657428

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Effects of analogs of indole-3-carbinol cyclic trimerization product in human breast cancer cells.

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Synthesis and biological evaluation of fused thio- and selenopyrans as new indolocarbazole analogues with aryl hydrocarbon receptor affinity

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Novel 3,3'-diindolylmethane derivatives: synthesis and cytotoxicity, structural characterization in solid state

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Cytostatic and antiestrogenic effects of 2-(indol-3-ylmethyl)-3,3'-diindolylmethane, a major in vivo product of dietary indole-3-carbinol

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10.3390/MOLECULES15064085

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8 February 2020

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8 February 2020

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8 February 2020

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