Studies toward bivalent κ opioids derived from Salvinorin A: heteromethylation of the furan ring reduces affinity

Munro, Thomas A, Xu, Wei, Ho, Douglas M, Liu-Chen, Lee-Yuan and Cohen, Bruce M 2013, Studies toward bivalent κ opioids derived from Salvinorin A: heteromethylation of the furan ring reduces affinity, Beilstein journal of organic chemistry, vol. 9, pp. 2916-2924, doi: 10.3762/bjoc.9.328.

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Title Studies toward bivalent κ opioids derived from Salvinorin A: heteromethylation of the furan ring reduces affinity
Author(s) Munro, Thomas AORCID iD for Munro, Thomas A orcid.org/0000-0002-3366-7149
Xu, Wei
Ho, Douglas M
Liu-Chen, Lee-Yuan
Cohen, Bruce M
Journal name Beilstein journal of organic chemistry
Volume number 9
Start page 2916
End page 2924
Total pages 9
Publisher Beilstein-Institut
Place of publication Frankfurt, Germany
Publication date 2013-12-20
ISSN 1860-5397
Keyword(s) JDTic
Salvinorin A
allotopic
bivalent ligand
designed multiple ligand
natural products
κ-opioid receptor
science and technology
physical sciences
chemistry
Language eng
DOI 10.3762/bjoc.9.328
Field of Research 030503 Organic Chemical Synthesis
060101 Analytical Biochemistry
0305 Organic Chemistry
HERDC Research category C1.1 Refereed article in a scholarly journal
ERA Research output type C Journal article
Copyright notice ©2013, Munro et al
Persistent URL http://hdl.handle.net/10536/DRO/DU:30093500

Document type: Journal Article
Collection: School of Life and Environmental Sciences
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