Design and Synthesis of Pyrazolomorphinan Derivatives as Novel Delta Opioid Receptor Agonists

We designed pyrazolomorphinan derivatives <b>3</b> as novel δ opioid receptor (DOR) selective agonists with an unprecedented chemotype according to the drug design concept for the DOR selective agonist KNT-127 which encompassed the message-address concept, the accessory site concept, and the conversion of an indole ring into a quinoline ring. The designed compounds <b>3</b> as well as their regioisomers <b>9</b> showed potent DOR agonistic activities with low or almost no activities for the μ (MOR) and κ opioid receptors (KOR). Among the tested compounds, SYK-1106 (<b>9j</b>) bearing a cyclohexyl substituent was the most potent and efficacious DOR agonist (DOR: EC<sub>50</sub> = 0.089 nM, <i>E</i><sub>max</sub> = 111%; agonistic activities for the MOR and KOR were not determined). SYK-1106 showed dose-dependent and DOR antagonist NTI reversible antidepressant-like effects at 0.3 mg/kg, s.c. in the mouse forced-swimming tests without an effect on locomotor activity and with no convulsive effects.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-12-03
DOI
https://doi.org/10.1021/acs.jmedchem.5c02499
Primary Topic
Neuropeptides and Animal Physiology
Type
article
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article

Design and Synthesis of Pyrazolomorphinan Derivatives as Novel Delta Opioid Receptor Agonists

H. Fujii, Chiharu Iwamatsu, Saki Ishizaki, Shigeto Hirayama et al.
Journal of Medicinal Chemistry
Neuropeptides and Animal Physiology
article

Design and Synthesis of Pyrazolomorphinan Derivatives as Novel Delta Opioid Receptor Agonists

H. Fujii, Chiharu Iwamatsu, Saki Ishizaki, Shigeto Hirayama, Fumika Karaki, Hideki Nakamura, Jun‐ichi Niwa, Shiro Shirakura, Akiyoshi Saitoh, Daisuke Yamada, Pengfei Liu, Toshinori Yoshioka, S. YAMADA
article en

Abstract

We designed pyrazolomorphinan derivatives <b>3</b> as novel δ opioid receptor (DOR) selective agonists with an unprecedented chemotype according to the drug design concept for the DOR selective agonist KNT-127 which encompassed the message-address concept, the accessory site concept, and the conversion of an indole ring into a quinoline ring. The designed compounds <b>3</b> as well as their regioisomers <b>9</b> showed potent DOR agonistic activities with low or almost no activities for the μ (MOR) and κ opioid receptors (KOR). Among the tested compounds, SYK-1106 (<b>9j</b>) bearing a cyclohexyl substituent was the most potent and efficacious DOR agonist (DOR: EC<sub>50</sub> = 0.089 nM, <i>E</i><sub>max</sub> = 111%; agonistic activities for the MOR and KOR were not determined). SYK-1106 showed dose-dependent and DOR antagonist NTI reversible antidepressant-like effects at 0.3 mg/kg, s.c. in the mouse forced-swimming tests without an effect on locomotor activity and with no convulsive effects.

Journal of Medicinal ChemistryVol. 68(24)
Tokyo University of Science (JP), Nippon Chemiphar (Japan) (JP), Pharmaceutical Biotechnology (Czechia) (CZ), Kitasato University (JP)
Openalex Percentile: Top 59%
Neuropeptides and Animal Physiology
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