Heteroatom-Substituted Analogues of Orphan Nuclear Receptor Small Heterodimer Partner Ligand and Apoptosis Inducer (E)-4-[3-(1-Adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic Acid-Reference-Cited by-同舟云学术

Heteroatom-Substituted Analogues of Orphan Nuclear Receptor Small Heterodimer Partner Ligand and Apoptosis Inducer (E)-4-[3-(1-Adamantyl)-4-hydroxyphenyl]-3-chlorocinnamic Acid

Published:2011-05-06 Issue:11 Volume:54 Page:3793-3816
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Xia Zebin¹,Farhana Lulu²,Correa Ricardo G.¹,Das Jayanta K.²,Castro David J.¹,Yu Jinghua¹,Oshima Robert G.¹,Reed John C.¹,Fontana Joseph A.²,Dawson Marcia I.¹

Affiliation:

1. Cancer Center, Sanford-Burnham Medical Research Institute, La Jolla, California 92037, United States

2. Department of Veterans Affairs Medical Center and Wayne State University School of Medicine, Detroit, Michigan 48201, United States

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm200051z

Reference78 articles.

1. Activation of the p38 and JNK/SAPK Mitogen-Activated Protein Kinase Pathways during Apoptosis Is Mediated by a Novel Retinoid

2. Induction of apoptosis of human B-CLL and ALL cells by a novel retinoid and its nonretinoidal analog

3. Antagonist Analogue of 6-[3‘-(1-Adamantyl)-4‘-hydroxyphenyl]-2-naphthalenecarboxylic Acid (AHPN) Family of Apoptosis Inducers That Effectively Blocks AHPN-Induced Apoptosis but Not Cell-Cycle Arrest

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