Dodecanoic acid derivatives: Synthesis, antimicrobial evaluation and development of one-target and multi-target QSAR models

被引:16
|
作者
Sarova, Devinder [2 ]
Kapoor, Archana [2 ]
Narang, Rakesh [2 ]
Judge, Vikramjeet [2 ]
Narasimhan, Balasubramanian [1 ]
机构
[1] Maharshi Dayanand Univ, Fac Pharmaceut Sci, Rohtak 124001, Haryana, India
[2] Guru Jambheshwar Univ Sci & Technol, Dept Pharmaceut Sci, Hisar 125001, Haryana, India
关键词
Dodecanoic acid derivatives; Antimicrobial activity; Ot-QSAR; Mt-QSAR; POLYUNSATURATED FATTY-ACIDS; ANTIFUNGAL ACTIVITY; IN-VITRO; ANTIMYCOBACTERIAL ACTIVITY; UNIFIED QSAR; PREDICTION; ANTIBACTERIAL; CHEMISTRY; NETWORKS;
D O I
10.1007/s00044-010-9383-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study a series of dodecanoic acid derivatives (1-30) were synthesized and evaluated for in vitro antimicrobial activity against the panel of Gram positive, Gram negative bacterial and fungal strains. 4-Nitro phenyl dodecanoate (4) and quinolin-8-yl dodecanoate (5) emerged as most effective antibacterial agents, and 1-(4-benzylpiperazin-1-yl) dodecan-1-one (15) was found to be the most effective antifungal agent amongst the synthesized dodecanoic acid derivatives. Quantitative structure activity relationship (QSAR) studies performed by the development of one-target and multi-target models indicated that multi-target model was effective in describing the antimicrobial activity of dodecanoic acid derivatives as well demonstrated the importance of topological parameter, zero-order molecular connectivity index ((0)chi).
引用
收藏
页码:769 / 781
页数:13
相关论文
共 50 条
  • [21] BET bromodomain inhibitors: fragment-based in silico design using multi-target QSAR models
    Alejandro Speck-Planche
    Marcus T. Scotti
    Molecular Diversity, 2019, 23 : 555 - 572
  • [22] Using the TOPS-MODE approach to fit multi-target QSAR models for tyrosine kinases inhibitors
    Marzaro, Giovanni
    Chilin, Adriana
    Guiotto, Adriano
    Uriarte, Eugenio
    Brun, Paola
    Castagliuolo, Ignazio
    Tonus, Francesca
    Gonzalez-Diaz, Humberto
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2011, 46 (06) : 2185 - 2192
  • [23] BET bromodomain inhibitors: fragment-based in silico design using multi-target QSAR models
    Speck-Planche, Alejandro
    Scotti, Marcus T.
    MOLECULAR DIVERSITY, 2019, 23 (03) : 555 - 572
  • [24] Role of Moving Average Analysis for Development of Multi-Target (Q)SAR Models
    Khatri, N.
    Dutt, R.
    Madan, A. K.
    MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2015, 15 (08) : 659 - 676
  • [25] First multi-target QSAR model for predicting the cytotoxicity of acrylic acid-based dental monomers
    Halder, Amit Kumar
    Delgado, Antonio H. S.
    Cordeiro, M. Natalia D. S.
    DENTAL MATERIALS, 2022, 38 (02) : 333 - 346
  • [26] Synthesis, antimicrobial evaluation and QSAR studies of p-coumaric acid derivatives
    Khatkar, Anurag
    Nanda, Arun
    Kumar, Pradeep
    Narasimhan, Balasubramanian
    ARABIAN JOURNAL OF CHEMISTRY, 2017, 10 : S3804 - S3815
  • [27] SYNTHESIS, ANTIMICROBIAL EVALUATION, QSAR AND IN SILICO ADMET STUDIES OF DECANOIC ACID DERIVATIVES
    Kumar, Ashwani
    Singh, Surender
    Jain, Sandeep
    Kumar, Parvin
    ACTA POLONIAE PHARMACEUTICA, 2011, 68 (02): : 191 - 204
  • [28] Predicting antiprotozoal activity of benzyl phenyl ether diamine derivatives through QSAR multi-target and molecular topology
    Garcia-Domenech, Ramon
    Zanni, Riccardo
    Galvez-Llompart, Maria
    Galvez, Jorge
    MOLECULAR DIVERSITY, 2015, 19 (02) : 357 - 366
  • [29] Predicting antiprotozoal activity of benzyl phenyl ether diamine derivatives through QSAR multi-target and molecular topology
    Ramon Garcia-Domenech
    Riccardo Zanni
    Maria Galvez-Llompart
    Jorge Galvez
    Molecular Diversity, 2015, 19 : 357 - 366
  • [30] Development of indolealkylamine derivatives as potential multi-target agents for COVID-19 treatment
    Chauhan, Jyoti
    Cecon, Erika
    Labani, Nedjma
    Gbahou, Florence
    Real, Fernando
    Bomsel, Morgane
    Dubey, Kshatresh Dutta
    Das, Ranajit
    Dam, Julie
    Jockers, Ralf
    Sen, Subhabrata
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 249