Non-vanillyl resiniferatoxin analogues as potent and metabolically stable transient receptor potential vanilloid 1 agonists-Reference-Cited by-同舟云学术

Non-vanillyl resiniferatoxin analogues as potent and metabolically stable transient receptor potential vanilloid 1 agonists

Published:2009-01 Issue:2 Volume:17 Page:690-698
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Choi Hyun-Kyung,Choi Sun,Lee Yoonji,Kang Dong Wook,Ryu HyungChul,Maeng Han-Joo,Chung Suk-Jae,Pavlyukovets Vladimir A.,Pearce Larry V.,Toth Attila,Tran Richard,Wang Yun,Morgan Matthew A.,Blumberg Peter M.,Lee Jeewoo

Publisher

Elsevier BV

Subject

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

Reference32 articles.

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3. Structure-activity Relations of Polyfunctional Diterpenes of the Daphnane Type. I. Revised Structure For Resiniferatoxin and Structure-activity Relations of Resini-feronol and Some of its Esters

4. Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analog of capsaicin, the irritant constituent in red pepper

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