Design, synthesis and molecular modeling study of acylated 1,2,4-triazole-3-acetates with potential anti-inflammatory activity

被引:97
作者
Abdel-Megeed, Ashraf M. [1 ]
Abdel-Rahman, Hamdy A. [1 ]
Alkaramany, Gamal-Eldien S. [1 ]
El-Gendy, Mahmoud A. [1 ]
机构
[1] Assiut Univ, Fac Pharm, Div Med Chem, Assiut 71526, Egypt
关键词
Heteroarylacetic acids; 1,2,4-Triazole; Acylation; Anti-inflammatory; Docking; COX-2; PHARMACOLOGICAL EVALUATION; ACID-DERIVATIVES; AGENTS; INHIBITORS; ANALOGS; ESTER;
D O I
10.1016/j.ejmech.2008.03.017
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The present investigation is concerned with the synthesis of different acylated 1,2,4-triazole-3-acetates with the objective of discovering novel and potent anti-inflammatory agents. Structures of the synthesized compounds were elucidated by spectral and elemental analyses. The obtained compounds were evaluated for their anti-inflammatory activites as well as gastric ulcerogenic effects and acute toxicity. Results showed that 1-acylated-5-amino-1,2,4-triazole-3-acetates 3a-e showed higher anti-inflammatory activity than the corresponding 5-acylamino derivatives 4a-e in carageenan-induced rat paw edema test with low gastric ulcerogenicity compared with indomethacin. Furthermore, molecular modeling studies were performed in order to rationalize the obtained biological results. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 23 条
  • [1] [Anonymous], 1980, Chem. Heterocycl.Compd. (Engl. Trans.), DOI [10.1007/BF00496616, DOI 10.1007/BF00496616]
  • [2] [Anonymous], 2005, MOL OP ENV MOE VERS
  • [3] Synthesis and anti-inflammatory activity of some [4,6-(4-substituted aryl)-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl]-acetic acid derivatives
    Bahekar, SS
    Shinde, DB
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (07) : 1733 - 1736
  • [4] Design and synthesis of some substituted 1H-pyrazolyl-oxazolidines or 1H-pyrazolyl-thiazolidines as anti-inflammatory-antimicrobial agents
    Bekhit, AA
    Fahmy, HTY
    [J]. ARCHIV DER PHARMAZIE, 2003, 336 (02) : 111 - 118
  • [5] 1,3,4-OXADIAZOLE, 1,3,4-THIADIAZOLE, AND 1,2,4-TRIAZOLE ANALOGS OF THE FENAMATES - IN-VITRO INHIBITION OF CYCLOOXYGENASE AND 5-LIPOXYGENASE ACTIVITIES
    BOSCHELLI, DH
    CONNOR, DT
    BORNEMEIER, DA
    DYER, RD
    KENNEDY, JA
    KUIPERS, PJ
    OKONKWO, GC
    SCHRIER, DJ
    WRIGHT, CD
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (13) : 1802 - 1810
  • [6] SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF ANTIINFLAMMATORY 1-METHYL-2-(4-X-BENZOYL)IMIDAZOLE-5-ACETIC ACIDS
    CALIENDO, G
    CIRINO, G
    GRECO, G
    NOVELLINO, E
    PERISSUTTI, E
    PINTO, A
    SANTAGADA, V
    SILIPO, C
    SORRENTINO, L
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1994, 29 (05) : 381 - 388
  • [7] 1,2,4-TRIAZOLES .6. SYNTHESIS OF NEW 1,5-DIPHENYL-3-1H-1,2,4-TRIAZOLES SUBSTITUTED WITH H-, ALKYL, OR CARBOXYL GROUPS AT C-3
    CZOLLNER, L
    SZILAGYI, G
    LANGO, J
    JANAKY, J
    [J]. ARCHIV DER PHARMAZIE, 1990, 323 (04) : 225 - 227
  • [8] Synthesis and pharmacological evaluation of 1-methyl-5-[substituted-4(3H)-oxo-1,2,3-benzotriazin-3-yl]-1H-pyrazole-4-acetic acid derivatives
    Daidone, G
    Maggio, B
    Plescia, S
    Raffa, D
    Schillaci, D
    Migliara, O
    Caruso, A
    Cutuli, VMC
    Amico-Roxas, M
    [J]. FARMACO, 1998, 53 (05): : 350 - 356
  • [9] Structural approaches to explain the selectivity of COX-2 inhibitors: Is there a common pharmacophore?
    Dannhardt, G
    Laufer, S
    [J]. CURRENT MEDICINAL CHEMISTRY, 2000, 7 (11) : 1101 - 1112
  • [10] Synthesis, structure and properties of N-acetylated derivatives of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate
    Dzygiel, A
    Rzeszotarska, B
    Masiukiewicz, E
    Cmoch, P
    Kamienski, B
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2004, 52 (02) : 192 - 198