Synthesis of Biologically Active Molecules through Multicomponent Reactions

被引:171
作者
Insuasty, Daniel [1 ]
Castillo, Juan [2 ,3 ]
Becerra, Diana [2 ]
Rojas, Hugo [2 ]
Abonia, Rodrigo [4 ]
机构
[1] Univ Norte, Dept Quim & Biol, Grp Invest Quim & Biol, Km 5 Via Puerto Colombia 1569, Barranquilla 081007, Atlantico, Colombia
[2] UPTC, Escuela Ciencias Quim, Grp Catalisis, Ave Cent Norte 39-115, Tunja 150003, Colombia
[3] Univ Los Andes, Dept Chem, Bioorgan Cpds Res Grp, Carrera 1 18A-10, Bogota 111711, Colombia
[4] Univ Valle, Dept Chem, Res Grp Heterocycl Cpds, Cali 25360, Colombia
关键词
multicomponent reactions (MCRs); medicinal chemistry; biological activity; drug discovery; ONE-POT SYNTHESIS; DIVERSITY-ORIENTED SYNTHESIS; 3 COMPONENT REACTION; BIQUINOLINE-PYRIDINE HYBRIDS; 3-COMPONENT SYNTHESIS; ANTICANCER ACTIVITY; ANTITUMOR-ACTIVITY; BIGINELLI REACTION; FACILE SYNTHESIS; 1,4-DIHYDROPYRIDINE DERIVATIVES;
D O I
10.3390/molecules25030505
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
Focusing on the literature progress since 2002, the present review explores the highly significant role that multicomponent reactions (MCRs) have played as a very important tool for expedite synthesis of a vast number of organic molecules, but also, highlights the fact that many of such molecules are biologically active or at least have been submitted to any biological screen. The selected papers covered in this review must meet two mandatory requirements: (1) the reported products should be obtained via a multicomponent reaction; (2) the reported products should be biologically actives or at least tested for any biological property. Given the diversity of synthetic approaches utilized in MCRs, the highly diverse nature of the biological activities evaluated for the synthesized compounds, and considering their huge structural variability, much of the reported data are organized into concise schemes and tables to facilitate comparison, and to underscore the key points of this review.
引用
收藏
页数:71
相关论文
共 235 条
[21]   Novel coumarin benzimidazole derivatives as antioxidants and safer anti-inflammatory agents [J].
Arora, Radha Krishan ;
Kaur, Navneet ;
Bansal, Yogita ;
Bansal, Gulshan .
ACTA PHARMACEUTICA SINICA B, 2014, 4 (05) :368-375
[22]   Novel spirooxindole-pyrrolidine compounds: Synthesis, anticancer and molecular docking studies [J].
Arun, Y. ;
Saranraj, K. ;
Balachandran, C. ;
Perumal, P. T. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 74 :50-64
[23]   Facile one-pot synthesis of novel dispirooxindole-pyrrolidine derivatives and their antimicrobial and anticancer activity against A549 human lung adenocarcinoma cancer cell line [J].
Arun, Y. ;
Bhaskar, G. ;
Balachandran, C. ;
Ignacimuthu, S. ;
Perumal, P. T. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (06) :1839-1845
[24]   Novel pyrano [3,2-b]xanthen-7(2H)-ones: Synthesis, antimicrobial, antioxidant and molecular docking studies [J].
Ashok, Dongamanti ;
Devulapally, Mohan Gandhi ;
Aamate, Vikas Kumar ;
Gundu, Srinivas ;
Adam, Shaik ;
Murthy, S. D. S. ;
Balasubramanian, Sridhar ;
Naveen, Baindla ;
Parthasarathy, Tigulla .
JOURNAL OF MOLECULAR STRUCTURE, 2019, 1177 :215-228
[26]   Recent applications of 1,3-thiazole core structure in the identification of new lead compounds and drug discovery [J].
Ayati, Adile ;
Emami, Saeed ;
Asadipour, Ali ;
Shafiee, Abbas ;
Foroumadi, Alireza .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2015, 97 :699-718
[27]   Coumarin: a potential nucleus for anti-inflammatory molecules [J].
Bansal, Yogita ;
Sethi, Purva ;
Bansal, Gulshan .
MEDICINAL CHEMISTRY RESEARCH, 2013, 22 (07) :3049-3060
[28]   Antibacterial studies of hydroxyspiro [indoline-3,9-xanthene] trione against spiro[indoline3,9-xanthene] trione and their use as acetyl and butyrylcholinesterase inhibitors [J].
Barmak, Alireza ;
Niknam, Khodabakhsh ;
Mohebbi, Gholamhossein ;
Pournabi, Hamid .
MICROBIAL PATHOGENESIS, 2019, 130 :95-99
[29]   Design, synthesis, structure-activity relationships, and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents [J].
Barreca, ML ;
Balzarini, J ;
Chimirri, A ;
De Clercq, E ;
De Luca, L ;
Höltje, HD ;
Höltje, M ;
Monforte, AM ;
Monforte, P ;
Pannecouque, C ;
Rao, A ;
Zappalà, M .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (24) :5410-5413
[30]   Synthesis of novel 5-arylidenethiazolidinones with apoptotic properties via a three component reaction using piperidine as a bifunctional reagent [J].
Bathula, Chandramohan ;
Tripathi, Sayantan ;
Srinivasan, Ramprasad ;
Jha, Kunal Kumar ;
Ganguli, Arnab ;
Chakrabarti, G. ;
Singh, Shailja ;
Munshi, Parthapratim ;
Sen, Subhabrata .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2016, 14 (34) :8053-8063