Antinociceptive activity of the novel fentanyl analogue iso-carfentanil in rats
Само за регистроване кориснике
2000
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
A large number of fentanyl analogues have been synthesized so far, both to establish the structure-activity-relationship (SAR) and to find novel, clinically useful antinociceptive drugs. In this study, the newly synthesized fentanyl analogue 3-carbomethoxy fentanyl (iso-carfentanil) was compared to fentanyl for its antinociceptive activity (tail-immersion test) in rats. It was revealed that the introduction of a 3-carbomethoxy group in the piperidine ring of fentanyl skeleton reduced the potency and shortened the duration of action of the parent compound, i.e., fentanyl. The antinociceptive potency of 3-carbomethoxy fentanyl is influenced mainly by the steric factor (voluminosity of the carbomethoxy group and the cis/trans isomerism), while the chemical nature of the group is probably irrelevant. This is in agreement with SAR studies of other 3-substituted fentanyl analogues. In contrast to potency, the duration of action is not affected by cis/trans isomerism. It is assumed that the t...ime course of action of 3-carbomethoxy fentanyl is influenced by the nature of the carbomethoxy group. Since the potency and the duration of action of this novel antinociceptive compound are interesting from the aspect of SAR studies and have potential promise for clinical application, 3-carbomethoxy fentanyl deserves to be extensively evaluated.
Кључне речи:
antinociception / fentanyl / carfentanil / structure-activity-relationshipИзвор:
Japanese Journal of Pharmacology, 2000, 84, 2, 188-195Издавач:
- Japanese Pharmacological Soc, Kyoto
Напомена:
- Free full text: https://doi.org/10.1254/jjp.84.188
DOI: 10.1254/jjp.84.188
ISSN: 0021-5198
PubMed: 11128042
WoS: 000090069100011
Scopus: 2-s2.0-0033763920
Колекције
Институција/група
Hemijski fakultet / Faculty of ChemistryTY - JOUR AU - Vuckovic, S AU - Prostran, M AU - Ivanović, Milovan AU - Ristovic, Z AU - Stojanović, R. PY - 2000 UR - https://cherry.chem.bg.ac.rs/handle/123456789/388 AB - A large number of fentanyl analogues have been synthesized so far, both to establish the structure-activity-relationship (SAR) and to find novel, clinically useful antinociceptive drugs. In this study, the newly synthesized fentanyl analogue 3-carbomethoxy fentanyl (iso-carfentanil) was compared to fentanyl for its antinociceptive activity (tail-immersion test) in rats. It was revealed that the introduction of a 3-carbomethoxy group in the piperidine ring of fentanyl skeleton reduced the potency and shortened the duration of action of the parent compound, i.e., fentanyl. The antinociceptive potency of 3-carbomethoxy fentanyl is influenced mainly by the steric factor (voluminosity of the carbomethoxy group and the cis/trans isomerism), while the chemical nature of the group is probably irrelevant. This is in agreement with SAR studies of other 3-substituted fentanyl analogues. In contrast to potency, the duration of action is not affected by cis/trans isomerism. It is assumed that the time course of action of 3-carbomethoxy fentanyl is influenced by the nature of the carbomethoxy group. Since the potency and the duration of action of this novel antinociceptive compound are interesting from the aspect of SAR studies and have potential promise for clinical application, 3-carbomethoxy fentanyl deserves to be extensively evaluated. PB - Japanese Pharmacological Soc, Kyoto T2 - Japanese Journal of Pharmacology T1 - Antinociceptive activity of the novel fentanyl analogue iso-carfentanil in rats VL - 84 IS - 2 SP - 188 EP - 195 DO - 10.1254/jjp.84.188 ER -
@article{ author = "Vuckovic, S and Prostran, M and Ivanović, Milovan and Ristovic, Z and Stojanović, R.", year = "2000", abstract = "A large number of fentanyl analogues have been synthesized so far, both to establish the structure-activity-relationship (SAR) and to find novel, clinically useful antinociceptive drugs. In this study, the newly synthesized fentanyl analogue 3-carbomethoxy fentanyl (iso-carfentanil) was compared to fentanyl for its antinociceptive activity (tail-immersion test) in rats. It was revealed that the introduction of a 3-carbomethoxy group in the piperidine ring of fentanyl skeleton reduced the potency and shortened the duration of action of the parent compound, i.e., fentanyl. The antinociceptive potency of 3-carbomethoxy fentanyl is influenced mainly by the steric factor (voluminosity of the carbomethoxy group and the cis/trans isomerism), while the chemical nature of the group is probably irrelevant. This is in agreement with SAR studies of other 3-substituted fentanyl analogues. In contrast to potency, the duration of action is not affected by cis/trans isomerism. It is assumed that the time course of action of 3-carbomethoxy fentanyl is influenced by the nature of the carbomethoxy group. Since the potency and the duration of action of this novel antinociceptive compound are interesting from the aspect of SAR studies and have potential promise for clinical application, 3-carbomethoxy fentanyl deserves to be extensively evaluated.", publisher = "Japanese Pharmacological Soc, Kyoto", journal = "Japanese Journal of Pharmacology", title = "Antinociceptive activity of the novel fentanyl analogue iso-carfentanil in rats", volume = "84", number = "2", pages = "188-195", doi = "10.1254/jjp.84.188" }
Vuckovic, S., Prostran, M., Ivanović, M., Ristovic, Z.,& Stojanović, R.. (2000). Antinociceptive activity of the novel fentanyl analogue iso-carfentanil in rats. in Japanese Journal of Pharmacology Japanese Pharmacological Soc, Kyoto., 84(2), 188-195. https://doi.org/10.1254/jjp.84.188
Vuckovic S, Prostran M, Ivanović M, Ristovic Z, Stojanović R. Antinociceptive activity of the novel fentanyl analogue iso-carfentanil in rats. in Japanese Journal of Pharmacology. 2000;84(2):188-195. doi:10.1254/jjp.84.188 .
Vuckovic, S, Prostran, M, Ivanović, Milovan, Ristovic, Z, Stojanović, R., "Antinociceptive activity of the novel fentanyl analogue iso-carfentanil in rats" in Japanese Journal of Pharmacology, 84, no. 2 (2000):188-195, https://doi.org/10.1254/jjp.84.188 . .