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Tytuł artykułu

One-pot synthesis of some novel N-aryl-1,4- dihydropyridines derivatives bearing nitrogen mustard

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The synthesis of a novel dihydropyridine, bearing carbethoxy groups at C(3) and C(5), respectively, has been achieved by applying three component Hantzsch-type condensation. The products were assayed for their in vitro biological assay antibacterial activity against with two Gram-positive bacteria Staphylococcus aureus MTCC-96, Streptococcus pyogenes MTCC 443, two Gram-negative bacteria Escherichia coli MTCC 442, Pseudomonas aeruginosa MTCC 441 and three fungal strains Candida albicans MTCC 227, Aspergillus Niger MTCC 282, Aspergillus clavatus MTCC 1323 taking ampicillin, chloramphenicol, ciprofloxacin, norfloxacin, nystatin, and griseofulvin as standard drugs.
Rocznik
Tom
Strony
61--67
Opis fizyczny
Bibliogr. 17 poz., tab., wz.
Twórcy
  • Department of Chemistry, Saurashtra University, Rajkot - 360005, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360005, India
Bibliografia
  • [1] (a) W. G. Mayler, Calcium Antagonist Academic Press, London (1989) (b) R. A. Janis, P. J. Silver and D. J. Triggle, Adv. Drug Res. 16 (1987) 309–391; (c) F. Bossert and W. Vater, Med. Res. Rev. 9 (1989) 291–324; (d) N. Martı´n and C. Seoane, Quim. Ind., 36 (1990) 115–127; (e) R. Peri, S. Padmanabhan, A. Rutledge, S. Singh and D. J. Triggle, J. Med. Chem. 43 (2000) 2906–2914; (f) S. Tasaka, H. Ohmori, N. Gomi, M. Iino, T. Machida, A. Kiue, S. Naito and M. Kuwano, Bioorg. Med. Chem. Lett. 11 (2001) 275– 277; (g) J. L. Harper, C. S. Camerini-Otero, A. Li, S. Kim, K. A. Jacobson and J. W. Daly, Biochem. Pharmacol. 65 (2003) 329–338; (h) A. A. S. Fernandes, M. S. Santos, J. A. F. Vicente, A. J. M. Moreno, Aa. Velena, G. Duburs and C. R. Oliveira, Mitochondrion 3 (2003) 47–59; (i) T. Okamura, T. Kikuchi, A. Nagamine, K. Fukushi, T. Sekine, Y. Arano and T. Irie, Free Radical Biol. Med. 38 (2005) 1197–1205.
  • [2] (a) U. Eisner and J. Kuthan, Chem. Rev. 72 (1972) 1–42; (b) D. M. Stout and A. I. Meyers, Chem. Rev. 82 (1982) 223–243; (c) F. Bossert, H. Meyer and E. Wehinger, Angew. Chem., Int. Ed. Engl. 1981, 20, 762–769; (d) J. Kuthan and A. Kurfu¨ rst, Ind. Eng. Chem. Prod. Res. Dev. 21 (1982) 191–261; (e) R. J. Chorvat and K. J. Roring, J. Org. Chem., 53 (1988) 5779–5781; (f) A. Guzman, M. Romero, A. Maddox and J. Muchowski, J. Org. Chem. 55 1990 5793–5797; (g) C. O. Kappe, Tetrahedron 49 (1993) 6937–6963; (h) L.M. Yagupolskii, I. I. Maletina, K. L. Petko, D. V. Fedyuk, R. Handrock, S. S. Shavaran, B. M. Klebanov and S. Herzig, J. Fluorine Chem. 109 (2001) 87–94; (i) C. Vela´ zquez and E. E. Knaus, Bioorg. Med. Chem. 12 2004 3831–3840. Vela´ zquez and E. E. Knaus, Bioorg. Med. Chem. 12 (2004) 3831–3840.
  • [3] D. h. Sriram; P. Yogeeswari; K. Madhu, Bioorg. Med. Chem. Lett. 15 (2005) 4502.
  • [4] B. Desai, D. Sureja, Y. Naliapara, A. Shah, A. K.Saxena, Bioorg. Med. Chem. 9 (2001) 1993.
  • [5] M. Khoshnevizadeh, N. Edraki, K. Javidnia, A. Alborzi, B. Pourabbas, J. Mardenah, R. Miri, Bioorg. Med. Chem. 17 (2009) 1579.
  • [6] A. T. Manvar, R. R. Pissurlenkar, V. R. Virsodia, K. D. Upadhyay, D. R. Manvar, A. K. Mishra, H. D. Acharya, A. R. Parecha, C. D. Dholakia, A. K. Shah, E. C. Coutinho, Mol.Divers., 14 (2010) 285.
  • [7] P. S. Kharkar, B. Desai, H. Gaveria, B. Varu, R. Loriya, Y. Naliapara,; A. Shah, V. Kulkarni, M. J. Med. Chem. 45 (2002) 4858.
  • [8] K. Sirisha,; G. Achaiah,; V. M. Reddy, Arch. Pharm. 6 (2010) 342.
  • [9] M. H. Cynamon, S. P. Klemens, T. S. Chou, R. H. Gimi, J. T. Weleh, J. Med. Chem. 35 (1992) 1212.
  • [10] M. H.Cynamon, R. H. Gimi, F. Gyenes, C. A. Sharpe, K. E. Bergmann, H.-J. Jan, L. B.Gregor, R. Rapolu, G. Luciano, J. T. Weleh, J. Med. Chem. 38 (1995) 3902.
  • [11] R. J. Speirs, J. T. Weleh, M. H. Cynamon, Antimicrob. Agents Chemother. 39 (1995) 1269. 12. G. A.Wachter, M. C. Davis, A. R. Martin, S. G. Franzblau, J. Med. Chem. 41 (1998) 2436.
  • [12] C. Viegas-Junior, A. Danuello, B.V. da Silva, E.J. Barreiro, C.A. Fraga, Curr. Med. Chem. 14 (2007) 1829-1852.
  • [13] V. R. Solomon, C. Hua, H. Lee, Bioorg. Med. Chem. 17 (2009) 7585-7592.
  • [14] A. R. Trivedi, D. K Dodiya, B. H. Dholariya, V. B. Kataria, V. R. Bhuva, V. H. Shah, Bioorganic & medicinal chemistry letters 21 (18) (2011) 5181-5183.
  • [15] A. Trivedi, D. Dodiya, B. Dholariya, V. Kataria, V. Bhuva, V. Shah, Chemical biology & drug design 78 (5), 2011, 881-886.
  • [16] Vogel’s Textbook of Practical Organic Chemistry, Fifth Edition, ELBS, Longman Scientific and Technical: England. (1989) Reprinted (1994) 1150.
  • [17] National Committee for Clinical and Laboratory Standards, Method for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically Approved Standard, fourth ed. NCCLS, Villanova, Italy, Document M 100-S7. (1997) S100-S157.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-57e60860-8487-49de-836e-eb945084f71c
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