Replacement of the hydrophobic part of 9-cis-retinoic acid with cyclic terpenoid moiety results in RXR-selective agonistic activity-Reference-Cited by-同舟云学术

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Replacement of the hydrophobic part of 9-cis-retinoic acid with cyclic terpenoid moiety results in RXR-selective agonistic activity

Published:2011-05 Issue:9 Volume:19 Page:2939-2949
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Okitsu Takashi,Sato Kana,Iwatsuka Kinya,Sawada Natsumi,Nakagawa Kimie,Okano Toshio,Yamada Shoya,Kakuta Hiroki,Wada Akimori

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference24 articles.

1. Orphan Nuclear Receptors: From Gene to Function

2. Design of selective nuclear receptor modulators: RAR and RXR as a case study

3. Co-regulator recruitment and the mechanism of retinoic acid receptor synergy

4. Structural Determinants of Allosteric Ligand Activation in RXR Heterodimers

5. Retinoid X Receptor Heterodimers in the Metabolic Syndrome

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1. Chemical Biology Studies Using Vitamin A Analogs;YAKUGAKU ZASSHI;2021-04-01

2. Concise Preparation and Biological Evaluations of 9-cis-Retinoic Acid Analogues Having an Aromatic Ring;HETEROCYCLES;2021

3. Pd ‐Catalyzed C  C Bond‐Forming Reactions;Applied Organic Chemistry;2020-12-11

4. Application of copper(i) salt and fluoride promoted Stille coupling reactions in the synthesis of bioactive molecules;Organic & Biomolecular Chemistry;2019

5. Interrupted carbonyl-olefin metathesis via oxygen atom transfer;Science;2018-09-28

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