Synthesis of heterocyclic ring-fused tricyclic diterpene analogs as novel inhibitors of RANKL-induced osteoclastogenesis and bone resorption-Reference-Cited by-同舟云学术

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Synthesis of heterocyclic ring-fused tricyclic diterpene analogs as novel inhibitors of RANKL-induced osteoclastogenesis and bone resorption

Published:2017-05 Issue: Volume:131 Page:48-67
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Wei Gao,Wu Yalan,He Xiao-Long,Liu Ting,Liu Mingyao,Luo Jian,Qiu Wen-Wei

Funder

Shanghai Science and Technology Council

National Key Technology R&D Program

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference41 articles.

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2. Safety and tolerability of denosumab for the treatment of postmenopausal osteoporosis;Lewiecki;Drug Healthc. Patient Saf.,2011

3. The complexities of skeletal biology;Karsenty;Nature,2003

4. Bisphosphonate-induced osteonecrosis of the jaw: a review of 2,400 patient cases;Filleul;J. Cancer Res. Clin. Oncol.,2010

5. Risks of hormone therapy in the 50-59 year age group;van de Weijer;Maturitas,2008

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3. Synthesis and Biological Evaluation of Heterocyclic Ring-Fused 20(S)-Protopanaxadiol Derivatives as Potent Antiosteoporosis Agents;Journal of Medicinal Chemistry;2023-08-19

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