Modeling of the D2 dopamine receptor arylpiperazine binding site for 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4-arylpiperazines
Samo za registrovane korisnike
2004
Autori
Šukalović, VladimirZlatović, Mario
Andrić, Deana
Roglić, Goran
Kostić Rajačić, Slađana
Šoškić, Vukić
Članak u časopisu (Objavljena verzija)
,
Wiley-VCH Verlag
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
Docking of several 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4- and 1-benzylarylpiperazines to the D 2 dopamine receptor (DAR) was examined. The binding pocket of the D 2 DAR defined according to Teeter and DuRand [1] was extended using the Insight II software. It was found that (i) the interaction of the protonated N1 of the piperazine ring with Asp86, (ii) the hydrogen bond formation between the benzimidazole part of the ligand and Ser141, as well as Ser122, and (iii) the edge-to-face interactions of the aromatic ring or arylpiperazine part of the ligand with Phe178, Tyr216 and Trp182 of the receptor represent the mayor stabilizing forces. Besides, the hydrogen bond acceptor group in position 2 of the phenylpiperazine aromatic ring could form one more hydrogen bond with Trp182. Bulky substituents in position 4 are not tolerated, due to the unfavorable sterical interaction with Phe178. Substituents in positions 2 and 3 are sterically well tolerated. Electron-attractive groups (F, Cl,... CF 3 , and NO 2 ) decreased, while electron donors (-OMe) and the second aromatic ring (naphthyl) increased the binding affinity, as compared to that of the parent compound 1. This can be explained by strong edge-to-face interactions of negative electrostatic surface potential (ESP) in the center of aromatic residues of the ligand with positive-ESP protons in the aromatic residues of the receptor. Thus, besides the salt bridges and hydrogen bonds, edge-to-face interactions significantly contribute to arylpiperazine ligands forming complexes with the D 2 DAR.
Ključne reči:
Arylpiperazines / D2 receptor / Binding pocketIzvor:
Archiv der Pharmazie, 2004, 337, 9, 502-512Izdavač:
- Wiley-VCH Verlag
DOI: 10.1002/ardp.200400901
ISSN: 0365-6233
PubMed: 15362123
WoS: 000224140000005
Scopus: 2-s2.0-4644326189
Institucija/grupa
IHTMTY - JOUR AU - Šukalović, Vladimir AU - Zlatović, Mario AU - Andrić, Deana AU - Roglić, Goran AU - Kostić Rajačić, Slađana AU - Šoškić, Vukić PY - 2004 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2822 AB - Docking of several 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4- and 1-benzylarylpiperazines to the D 2 dopamine receptor (DAR) was examined. The binding pocket of the D 2 DAR defined according to Teeter and DuRand [1] was extended using the Insight II software. It was found that (i) the interaction of the protonated N1 of the piperazine ring with Asp86, (ii) the hydrogen bond formation between the benzimidazole part of the ligand and Ser141, as well as Ser122, and (iii) the edge-to-face interactions of the aromatic ring or arylpiperazine part of the ligand with Phe178, Tyr216 and Trp182 of the receptor represent the mayor stabilizing forces. Besides, the hydrogen bond acceptor group in position 2 of the phenylpiperazine aromatic ring could form one more hydrogen bond with Trp182. Bulky substituents in position 4 are not tolerated, due to the unfavorable sterical interaction with Phe178. Substituents in positions 2 and 3 are sterically well tolerated. Electron-attractive groups (F, Cl, CF 3 , and NO 2 ) decreased, while electron donors (-OMe) and the second aromatic ring (naphthyl) increased the binding affinity, as compared to that of the parent compound 1. This can be explained by strong edge-to-face interactions of negative electrostatic surface potential (ESP) in the center of aromatic residues of the ligand with positive-ESP protons in the aromatic residues of the receptor. Thus, besides the salt bridges and hydrogen bonds, edge-to-face interactions significantly contribute to arylpiperazine ligands forming complexes with the D 2 DAR. PB - Wiley-VCH Verlag T2 - Archiv der Pharmazie T1 - Modeling of the D2 dopamine receptor arylpiperazine binding site for 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4-arylpiperazines VL - 337 IS - 9 SP - 502 EP - 512 DO - 10.1002/ardp.200400901 ER -
@article{ author = "Šukalović, Vladimir and Zlatović, Mario and Andrić, Deana and Roglić, Goran and Kostić Rajačić, Slađana and Šoškić, Vukić", year = "2004", abstract = "Docking of several 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4- and 1-benzylarylpiperazines to the D 2 dopamine receptor (DAR) was examined. The binding pocket of the D 2 DAR defined according to Teeter and DuRand [1] was extended using the Insight II software. It was found that (i) the interaction of the protonated N1 of the piperazine ring with Asp86, (ii) the hydrogen bond formation between the benzimidazole part of the ligand and Ser141, as well as Ser122, and (iii) the edge-to-face interactions of the aromatic ring or arylpiperazine part of the ligand with Phe178, Tyr216 and Trp182 of the receptor represent the mayor stabilizing forces. Besides, the hydrogen bond acceptor group in position 2 of the phenylpiperazine aromatic ring could form one more hydrogen bond with Trp182. Bulky substituents in position 4 are not tolerated, due to the unfavorable sterical interaction with Phe178. Substituents in positions 2 and 3 are sterically well tolerated. Electron-attractive groups (F, Cl, CF 3 , and NO 2 ) decreased, while electron donors (-OMe) and the second aromatic ring (naphthyl) increased the binding affinity, as compared to that of the parent compound 1. This can be explained by strong edge-to-face interactions of negative electrostatic surface potential (ESP) in the center of aromatic residues of the ligand with positive-ESP protons in the aromatic residues of the receptor. Thus, besides the salt bridges and hydrogen bonds, edge-to-face interactions significantly contribute to arylpiperazine ligands forming complexes with the D 2 DAR.", publisher = "Wiley-VCH Verlag", journal = "Archiv der Pharmazie", title = "Modeling of the D2 dopamine receptor arylpiperazine binding site for 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4-arylpiperazines", volume = "337", number = "9", pages = "502-512", doi = "10.1002/ardp.200400901" }
Šukalović, V., Zlatović, M., Andrić, D., Roglić, G., Kostić Rajačić, S.,& Šoškić, V.. (2004). Modeling of the D2 dopamine receptor arylpiperazine binding site for 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4-arylpiperazines. in Archiv der Pharmazie Wiley-VCH Verlag., 337(9), 502-512. https://doi.org/10.1002/ardp.200400901
Šukalović V, Zlatović M, Andrić D, Roglić G, Kostić Rajačić S, Šoškić V. Modeling of the D2 dopamine receptor arylpiperazine binding site for 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4-arylpiperazines. in Archiv der Pharmazie. 2004;337(9):502-512. doi:10.1002/ardp.200400901 .
Šukalović, Vladimir, Zlatović, Mario, Andrić, Deana, Roglić, Goran, Kostić Rajačić, Slađana, Šoškić, Vukić, "Modeling of the D2 dopamine receptor arylpiperazine binding site for 1-{2-[5-(1H-benzimidazole-2-thione)]ethyl}-4-arylpiperazines" in Archiv der Pharmazie, 337, no. 9 (2004):502-512, https://doi.org/10.1002/ardp.200400901 . .