Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Ivanović Milovan"'
Autor:
Jevtić Ivana I., Penjišević Jelena Z., Savić-Vujović Katarina R., Srebro Dragana P., Vučković Sonja M., Ivanović Milovan D., Kostić-Rajačić Slađana V.
Publikováno v:
Journal of the Serbian Chemical Society, Vol 85, Iss 6, Pp 711-720 (2020)
Herein, the synthesis and pharmacological evaluation of 13 novel compounds, designed as potential heterobivalent ligands for μ-opioid receptor (MOR) and dopamine D2 receptors (D2DAR), are reported. The compounds consisted of anilido piperidine and N
Externí odkaz:
https://doaj.org/article/9a224bd97bb9405aab39da7b126ece23
Publikováno v:
Journal of the Serbian Chemical Society, Vol 84, Iss 7, Pp 639-647 (2019)
A scalable, cost-efficient and simple synthetic pathway towards potential bivalent opioid/dopamine receptor ligands was developed and optimized. Three novel compounds that contain both opioid and dopamine pharmacophores linked by the four methylene g
Externí odkaz:
https://doaj.org/article/1bc32f98f1f44fa199620f2d1c4f97b2
Publikováno v:
Hemijska Industrija, Vol 69, Iss 5, Pp 523-536 (2015)
Glutarimides, 2,6-dioxopiperidines are compounds that rarely occur in natural sources, but so far isolated ones exert widespread pharmacological activities, which makes them valuable as potential pharmacotherapeutics. Glutarimides act as androgen
Externí odkaz:
https://doaj.org/article/137029d4968040cbabaf1ff18b81cfab
Publikováno v:
Journal of the Serbian Chemical Society, Vol 74, Iss 11, Pp 1207-1217 (2009)
The δ-opioid receptor is sensitive to ligand geometry. In order to assist the synthesis of new δ-selective opioid ligands, the structure elements of δ-selective opioid ligands necessary for their effective binding were investigated. The automated
Externí odkaz:
https://doaj.org/article/18e97c74691448a7b11b58ee6030c943
Publikováno v:
Journal of the Serbian Chemical Society, Vol 72, Iss 7, Pp 643-654 (2007)
Fentanyl is a highly potent and clinically widely used narcotic analgesic. The synthesis of its analogs remains a challenge in an attempt to develop highly selective µ-opioid receptor agonists with specific pharmacological properties. In this paper,
Externí odkaz:
https://doaj.org/article/d3bd83da30b544feac0496cd98bcd240
Autor:
Ivanović Milovan D., Mićović I.V., Vučković Sonja M., Prostran Milica Š., Todorović Zoran M., Kricojević V.D., Đorđević J.B., Došen-Mićović Ljiljana I.
Publikováno v:
Journal of the Serbian Chemical Society, Vol 69, Iss 7, Pp 511-526 (2004)
A general, five step method for the synthesis of 3-alkylfentanyl analogues (i.e., cis and trans 3-alkyl-4-anilidopiperidines 6.1–6.6) has been developed. The starting N-phenethyl- 4-piperidone 1 was first converted into the cyclohexylimine derivati
Externí odkaz:
https://doaj.org/article/87b18d5918ee4a109bf3aa5c816ccb74
Autor:
Ivanović Milovan D., Mićović I.V., Vučković Sonja M., Prostran Milica Š., Todorović Zoran M., Ivanović Evica R., Kiricojević Vesna D., Đorđević J.B., Došen-Mićović Ljiljana I.
Publikováno v:
Journal of the Serbian Chemical Society, Vol 69, Iss 11, Pp 955-968 (2004)
An efficient, five-step synthetic approach to various acyclic 1,3-diamines has been developed and applied to the preparation of a novel class of open-chained fentanyl analogues. The acyclic derivatives 5.1–5.5 (all new compounds) were synthesized w
Externí odkaz:
https://doaj.org/article/45b6a12468a347489950895914c7ff92
Autor:
Vučković Sonja M., Prostran Milica Š., Ivanović Milovan D., Todorović Zoran M., Stojanović Radan M., Nešić Zorica I., Matić Ivana, Milovanović Slobodan R.
Publikováno v:
Vojnosanitetski Pregled, Vol 61, Iss 4, Pp 413-421 (2004)
Externí odkaz:
https://doaj.org/article/93c29f54057f41c48822c3ab1d283bcb
Autor:
Kiricojević Vesna D., Ivanović Milovan D., Mićović I.V., Đorđević J.B., Roglić Goran M., Došen-Mićović Ljiljana I.
Publikováno v:
Journal of the Serbian Chemical Society, Vol 67, Iss 12, Pp 793-802 (2002)
An efficient synthesis of methyl 4-[(1-oxopropyl)phenylamino]piperidine-4-carboxylate (7) has been developed starting from 1-benzylpiperidin-4-one (1). The compound is a key intermediate in the synthesis of new generation, highly active narcotic anal
Externí odkaz:
https://doaj.org/article/0277921e67744638877e535414c5a4a7
Autor:
Krunić, Mihajlo, Penjišević, Jelena, Jevtić, Ivana, Ivanović, Milovan, Kostić-Rajačić, Slađana
Publikováno v:
Book of Abstracts-26th EFMC-ISMC, International Symposium on Medicinal Chemistry, Aug. 29-Sept. 2, 2021, virtual event
Alzheimer’s disease (AD) is a neurodegenerative disease which affects over 50 milion people worldwide.1) AD mainly affects people ages 65 and above. Symptoms are memory loss, decline in learning capacity, and language problems. One of currently ava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4273::4c587c97a3cba6e9a489435dcc4e8eb3
https://hdl.handle.net/21.15107/rcub_cer_5843
https://hdl.handle.net/21.15107/rcub_cer_5843
