Mild Synthetic Approach to Novel Indole-1-Carbinols and Preliminary Evaluation of Their Cytotoxicity in Hepatocarcinoma Cells

Asymmetric Organocatalytic N-Alkylation of Indole-2-carbaldehydes with α,β-Unsaturated Aldehydes: One-Pot Synthesis of Chiral Pyrrolo[1,2-a]indole-2-carbaldehydes

(2009) Liang Hong et al.   CHEMISTRY-A EUROPEAN JOURNAL

Targeting of the Akt-Nuclear Factor- B Signaling Network by [1-(4-Chloro-3-nitrobenzenesulfonyl)-1H-indol-3-yl]-methanol (OSU-A9), a Novel Indole-3-Carbinol Derivative, in a Mouse Model of Hepatocellular Carcinoma

(2009) H. A. Omar et al.   MOLECULAR PHARMACOLOGY

Reduction of 1-pyrrolyl and 1-indolyl carbamates to hemiaminals

(2009) He-Chu Hsu et al.   TETRAHEDRON LETTERS

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

(2008) Jing-Ru Weng et al.   CANCER LETTERS

Discovery of 4-Aryl-4H-chromenes as a New Series of Apoptosis Inducers Using a Cell- and Caspase-Based High Throughput Screening Assay. 4. Structure–Activity Relationships ofN-Alkyl Substituted Pyrrole Fused at the 7,8-Positions

(2008) William Kemnitzer et al.   JOURNAL OF MEDICINAL CHEMISTRY

Characterization of a Three-Component Coupling Reaction on Proteins by Isotopic Labeling and Nuclear Magnetic Resonance Spectroscopy

(2008) Jesse M. McFarland et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY