Synthesis, characterization and antimicrobial activity of some new dihydropyrano[c]chromenes

• Autorzy: Bhalu A. , Moteriya P. , Chanda S. , Baluja S.
• Języki publikacji: EN

Abstrakty

EN

Some new dihydropyrano[c]chromenes derivatives are synthesized from 4-hydroxycoumarin. The structure of newly synthesized compounds was confirmed by mass, 1H NMR and IR spectroscopy. Further, antimicrobial screening of these synthesized compounds was done against some bacterial (Gram positive as well as Gram negative) and fungal strains in N,N-dimethylformamide. It is observed that some of synthesized compounds exhibited significant antibacterial activity against Gram positive bacterial strains. The selected fungal strains were most resistant for the studied compounds as none of the synthesized compounds showed activity against any of the fungal strain studied. The best antibacterial activity was shown by ABR-10.

Słowa kluczowe

EN

Dihydropyrano[c]chromenes; antibacterial activity; Gram positive bacteria; Gram negative bacteria; N,N-Dimethylformamide

• Wydawca: Przedsiębiorstwo Wydawnictw Naukowych "DARWIN"
• Czasopismo: International Letters of Chemistry, Physics and Astronomy
• Rocznik: 2014
• Tom: Vol. 12
• Strony: 1--6
• Opis fizyczny: Bibliogr. 10 poz., rys., tab., wz.

Twórcy

autor

Bhalu A.

• Department of Chemistry, Saurashtra University, Rajkot 360005, India

autor

Moteriya P.

• Department of Bioscience, Saurashtra University, Rajkot 360005, India

autor

Chanda S.

• Department of Bioscience, Saurashtra University, Rajkot 360005, India

autor

Baluja S.

• Department of Chemistry, Saurashtra University, Rajkot 360005, India

Bibliografia

• [1] Trapkov VA, Parfenov EA, Smirnov LD. Pharm. Chem. J. 30 (1996) 445-447.
• [2] Vukovic N, Sukdolak S, Solujic S, Niciforovic N. Arch. Pharm. Res. 33 (2010) 5-15.
• [3] Emmanuel-Giota AA, Fylaktakidou KC, Hadjipavlou-Litina DJ, Litinas KE, Nicolaides DN., J. Heterocyclic Chem. 38 (2001) 717-722.
• [4] Hamdi N, Dixneuf PH. Topics in Heterocyclic Chemistry, Springer-Verlag, BerlinHeidelberg, 2007.
• [5] Basanagouda M, Kulkarni MV, Sharma D, Gupta VK, Sandhyarani P, Sasal VP. J. Chem. Sci. 121 (2009) 485-495.
• [6] Liu X, Dong M, Chen X, Jiang M, Lv X, Zhou J., Appl Microbiol Biotechnol. 78 (2008) 241-247.
• [7] Wang M, Wang L, Li Y, Li Q., Trans. Met. Chem. 26 (2001) 307-310.
• [8] Marchenko MM, Kopyl’chuk GP, Shmarakov IA, Ketsa OV, Kushnir VN, Pharm. Chem. J. 40 (2006) 296-297.
• [9] Perez C, Paul M, Bazerque P., Acta Biol Med Exp 15 (1990) 113-115.
• [10] Baluja S, Parekh J, Chanda S, Vaishnani KP, J Indian Chem Soc 86 (2009) 1338-1342.