Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents
Само за регистроване кориснике
2012
Аутори
Trisović, NemanjaTimić, Tamara

Divljaković, Jovana
Rogan, Jelena
Poleti, Dejan
Savić, Miroslav

Uscumlić, Gordana
Чланак у часопису (Објављена верзија)

Метаподаци
Приказ свих података о документуАпстракт
Considering the importance of hydantoin derivatives in treatment of status epilepticus, four 5-phenylhydantoins, whose lipophilicities were estimated to be similar to that of phenytoin, were synthesized. Evaluation of their anticonvulsant activities was performed on rats by subcutaneous pentylenetetrazol seizure test and intravenous pentylenetetrazol threshold test, and spontaneous locomotor activity test was used to assess possible sedative effects. X-ray analysis of three compounds suggested that certain analogies might be drawn between interactions in crystal packing and biological interactions responsible for their anticonvulsant activity. It was found that 5-ethyl-5-phenyl-3-propylhydantoin exhibits the most favorable pharmacological properties among the synthesized compounds, i.e., anticonvulsant activity comparable to phenytoin with lower liability for induction of sedation in rats.
Кључне речи:
Hydantoin derivatives / Anticonvulsant activity / Sedative effects / Crystal structureИзвор:
Monatshefte für Chemie Chemical Monthly, 2012, 143, 10, 1451-1457Издавач:
- Springer Wien, Wien
Финансирање / пројекти:
- Проучавање синтезе, структуре и активности органских једињења природног и синтетског порекла (RS-172013)
DOI: 10.1007/s00706-012-0791-8
ISSN: 0026-9247
WoS: 000309253500015
Scopus: 2-s2.0-84867096117
Институција/група
PharmacyTY - JOUR AU - Trisović, Nemanja AU - Timić, Tamara AU - Divljaković, Jovana AU - Rogan, Jelena AU - Poleti, Dejan AU - Savić, Miroslav AU - Uscumlić, Gordana PY - 2012 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1649 AB - Considering the importance of hydantoin derivatives in treatment of status epilepticus, four 5-phenylhydantoins, whose lipophilicities were estimated to be similar to that of phenytoin, were synthesized. Evaluation of their anticonvulsant activities was performed on rats by subcutaneous pentylenetetrazol seizure test and intravenous pentylenetetrazol threshold test, and spontaneous locomotor activity test was used to assess possible sedative effects. X-ray analysis of three compounds suggested that certain analogies might be drawn between interactions in crystal packing and biological interactions responsible for their anticonvulsant activity. It was found that 5-ethyl-5-phenyl-3-propylhydantoin exhibits the most favorable pharmacological properties among the synthesized compounds, i.e., anticonvulsant activity comparable to phenytoin with lower liability for induction of sedation in rats. PB - Springer Wien, Wien T2 - Monatshefte für Chemie Chemical Monthly T1 - Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents VL - 143 IS - 10 SP - 1451 EP - 1457 DO - 10.1007/s00706-012-0791-8 ER -
@article{ author = "Trisović, Nemanja and Timić, Tamara and Divljaković, Jovana and Rogan, Jelena and Poleti, Dejan and Savić, Miroslav and Uscumlić, Gordana", year = "2012", abstract = "Considering the importance of hydantoin derivatives in treatment of status epilepticus, four 5-phenylhydantoins, whose lipophilicities were estimated to be similar to that of phenytoin, were synthesized. Evaluation of their anticonvulsant activities was performed on rats by subcutaneous pentylenetetrazol seizure test and intravenous pentylenetetrazol threshold test, and spontaneous locomotor activity test was used to assess possible sedative effects. X-ray analysis of three compounds suggested that certain analogies might be drawn between interactions in crystal packing and biological interactions responsible for their anticonvulsant activity. It was found that 5-ethyl-5-phenyl-3-propylhydantoin exhibits the most favorable pharmacological properties among the synthesized compounds, i.e., anticonvulsant activity comparable to phenytoin with lower liability for induction of sedation in rats.", publisher = "Springer Wien, Wien", journal = "Monatshefte für Chemie Chemical Monthly", title = "Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents", volume = "143", number = "10", pages = "1451-1457", doi = "10.1007/s00706-012-0791-8" }
Trisović, N., Timić, T., Divljaković, J., Rogan, J., Poleti, D., Savić, M.,& Uscumlić, G.. (2012). Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents. in Monatshefte für Chemie Chemical Monthly Springer Wien, Wien., 143(10), 1451-1457. https://doi.org/10.1007/s00706-012-0791-8
Trisović N, Timić T, Divljaković J, Rogan J, Poleti D, Savić M, Uscumlić G. Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents. in Monatshefte für Chemie Chemical Monthly. 2012;143(10):1451-1457. doi:10.1007/s00706-012-0791-8 .
Trisović, Nemanja, Timić, Tamara, Divljaković, Jovana, Rogan, Jelena, Poleti, Dejan, Savić, Miroslav, Uscumlić, Gordana, "Synthesis, structural and biological characterization of 5-phenylhydantoin derivatives as potential anticonvulsant agents" in Monatshefte für Chemie Chemical Monthly, 143, no. 10 (2012):1451-1457, https://doi.org/10.1007/s00706-012-0791-8 . .