The determination of the absolute configuration of a chiral 2,3'-diindolylarylmethane by NMR spectroscopy.

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The determination of the absolute configuration of a chiral 2,3'-diindolylarylmethane by NMR spectroscopy.

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The determination of the absol ...... ylmethane by NMR spectroscopy.

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The determination of the absol ...... ylmethane by NMR spectroscopy.

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The determination of the absol ...... ylmethane by NMR spectroscopy.

@en

The determination of the absol ...... ylmethane by NMR spectroscopy.

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The determination of the absol ...... ylmethane by NMR spectroscopy.

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The determination of the absol ...... ylmethane by NMR spectroscopy.

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P1476

The determination of the absol ...... ylmethane by NMR spectroscopy.

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P2093

Chuan-Qing Kang

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Fu-She Han

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Shuai Qi

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Peroxisome proliferator-activated receptor gamma-dependent activity of indole ring-substituted 1,1-bis(3'-indolyl)-1-(p-biphenyl)methanes in cancer cells.

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Antiproliferative acetogenins from a Uvaria sp. from the Madagascar dry forest.

Combining radiation and molecular targeting in cancer therapy.

Application of electronic circular dichroism in configurational and conformational analysis of organic compounds.

Cancer chemotherapy with indole-3-carbinol, bis(3'-indolyl)methane and synthetic analogs.

1,1-bis(3'-indolyl)-1-(p-substituted phenyl)methanes decrease mitochondrial membrane potential and induce apoptosis in endometrial and other cancer cell lines

1,1-bis(3'-indolyl)-1-(p-substitutedphenyl)methanes inhibit growth, induce apoptosis, and decrease the androgen receptor in LNCaP prostate cancer cells through peroxisome proliferator-activated receptor gamma-independent pathways.

A novel ring-substituted diindolylmethane,1,1-bis[3'-(5-methoxyindolyl)]-1-(p-t-butylphenyl) methane, inhibits extracellular signal-regulated kinase activation and induces apoptosis in acute myelogenous leukemia.

Chiral aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole template: synthesis, absolute configuration, and in vitro activity.

P304

181-187

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P31

scholarly article

P356

10.1002/MRC.4192

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-01-22T00:00:00Z

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P698

25612164

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