Design, synthesis, computational and biological evaluation of new anxiolytics

被引:128
作者
Geronikaki, A [1 ]
Babaev, E
Dearden, J
Dehaen, W
Filimonov, D
Galaeva, I
Krajneva, V
Lagunin, A
Macaev, F
Molodavkin, G
Poroikov, V
Pogrebnoi, S
Saloutin, V
Stepanchikova, A
Stingaci, E
Tkach, N
Vlad, L
Voronina, T
机构
[1] Aristotle Univ Thessaloniki, Dept Pharmaceut Chem, Sch Pharm, Thessaloniki 54124, Greece
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
[3] Liverpool John Moores Univ, Sch Pharm & Chem, Liverpool L3 3AF, Merseyside, England
[4] Catholic Univ Louvain, B-3001 Louvain, Belgium
[5] Russian Acad Med Sci, Inst Biomed Chem, Moscow 119121, Russia
[6] Russian Acad Med Sci, Inst Pharmacol, Moscow 125315, Russia
[7] Moldavian Acad Sci, Inst Chem, MD-2028 Kishinev, Moldova
[8] Russian Acad Sci, Inst Organ Chem, Urals Div, Ekaterinburg 620219, Russia
关键词
anxiolytics; synthesis; thiazoles; pyrazoles; 2-indolinones; fused imidazoles; PASS;
D O I
10.1016/j.bmc.2004.09.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
New anxiolytics have been discovered by prediction of biological activity with computer programs PASS and DEREK for a heterogeneous set of 5494 highly chemically diverse heterocyclic compounds (thiazoles, pyrazoles, isatins, a-fused imidazoles and others). The majority of tested compounds exhibit the predicted anxiolytic effect. The most potent activity was found in 2-(4-nitrophenyl)-3-(4-phenylpiperazinomethyl)imidazo[1,2-a]pyridine 8, 1-[(4-bromophenyl)-2-oxoethyl]-3-(1,3-dioxolano)-2-indolinone 3, 5hydroxy-3-methoxycarbonyl-l-phenylpyrazole 5 and 2-(4-fluorophenyl)-3-(4-methylpiperazinomethyl)imidazo[1,2-cr]pyridine 7. The application of the computer-assisted approach significantly reduced the number of synthesized and tested compounds and increased the chance of finding new chemical entities (NCEs). circle dot 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6559 / 6568
页数:10
相关论文
共 51 条
  • [21] Effects of the novel analgesic, cizolirtine, in a rat model of neuropathic pain
    Kayser, V
    Farré, A
    Hamon, M
    Bourgoin, S
    [J]. PAIN, 2003, 104 (1-2) : 169 - 177
  • [22] ANTI-INFLAMMATORY AGENTS .17. 4.5-BIS-(4-METHOXYPHENYL)-2-(ARYLTHIO)AZOLES WITH ANTI-INFLAMMATORY ACTIVITY
    KLOSE, W
    NIEDBALLA, U
    SCHWARZ, K
    BOTTCHER, I
    [J]. ARCHIV DER PHARMAZIE, 1983, 316 (11) : 941 - 951
  • [23] Computer-aided selection of potential antihypertensive compounds with dual mechanism of action
    Lagunin, AA
    Gomazkov, OA
    Filimonov, DA
    Gureeva, TA
    Dilakyan, EA
    Kugaevskaya, EV
    Elisseeva, YE
    Solovyeva, NI
    Poroikov, VV
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (15) : 3326 - 3332
  • [24] LAKHAN R, 1986, FARMACO, V41, P788
  • [25] Lange J, 2001, Acta Pol Pharm, V58, P43
  • [26] Selecting screening candidates for kinase and G protein-coupled receptor targets using neural networks
    Manallack, DT
    Pitt, WR
    Gancia, E
    Montana, JG
    Livingstone, DJ
    Ford, MG
    Whitley, DC
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 2002, 42 (05): : 1256 - 1262
  • [27] IMIDAZO[2,1-B]BENZOTHIAZOLES .2. NEW IMMUNOSUPPRESSIVE AGENTS
    MASE, T
    ARIMA, H
    TOMIOKA, K
    YAMADA, T
    MURASE, K
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (03) : 386 - 394
  • [28] Molodavkin G. M., 1995, Eksperimental'naya i Klinicheskaya Farmakologiya, V58, P54
  • [29] Nash Lawrence T, 2002, Expert Opin Pharmacother, V3, P555
  • [30] POTENTIAL ANTI-CONVULSANTS .6. CONDENSATION OF ISATINS WITH CYCLOHEXANONE AND OTHER CYCLIC-KETONES
    PAJOUHESH, H
    PARSON, R
    POPP, FD
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (03) : 318 - 321