2021
DOI: 10.3390/molecules26185448
|View full text |Cite
|
Sign up to set email alerts
|

Biological Effects on μ-Receptors Affinity and Selectivity of Arylpropenyl Chain Structural Modification on Diazatricyclodecane Derivatives

Abstract: Opioid analgesics are clinically used to relieve severe pain in acute postoperative and cancer pain, and also in the long term in chronic pain. The analgesic action is mediated by μ-, δ-, and κ-receptors, but currently, with few exceptions for k-agonists, μ-agonists are the only ones used in therapy. Previously synthesized compounds with diazotricyclodecane cores (DTDs) have shown their effectiveness in binding opioid receptors. Fourteen novel diazatricyclodecanes belonging to the 9-propionyl-10-substituted-9,… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 34 publications
0
2
0
Order By: Relevance
“…The Supporting Information is available free of charge on the Wiley VCH GmbH Publications website: Experimental protocols, nuclear magnetic resonance spectra, HPLC traces and X‐ray crystallographic data. Additional references are cited within the Supporting Information [30–59] …”
Section: Supporting Informationmentioning
confidence: 99%
“…The Supporting Information is available free of charge on the Wiley VCH GmbH Publications website: Experimental protocols, nuclear magnetic resonance spectra, HPLC traces and X‐ray crystallographic data. Additional references are cited within the Supporting Information [30–59] …”
Section: Supporting Informationmentioning
confidence: 99%
“…The Supporting Information is available free of charge on the Wiley VCH GmbH Publications website: Experimental protocols, nuclear magnetic resonance spectra, HPLC traces and X‐ray crystallographic data. Additional references are cited within the Supporting Information [30–59] …”
Section: Supporting Informationmentioning
confidence: 99%