Asian Journal of Research in Chemistry

Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Synthesis Characterization and Antimicrobial Activities of Schiff bases of 3-Formyl chromones


Affiliations
1 Assistant Professor, Department of Chemistry, Kisan PG College Babhnan, Gonda, India., India
2 Associate Professor, Department of Chemistry, KS Saket PG College Ayodhya, India., India
     

   Subscribe/Renew Journal


The present paper is all about the synthesis of some novel schiff bases of chromones. The structure conformation of ligand molecule is done by using various spectroscopic techniques such as 1H NMR, IR and elemental analysis. The antibacterial and anti-fungal activities of synthesized complexes were tested according to standard procedure.

Keywords

Schiff base, Chromones, Antibacterial activity, Anti-fungal activity, Pharmacological activity, Condensation, H1NMR, IR, etc.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Egorov A M, Ulyashova M M & Rubtsova M Y, Acta Naturae, 10 (2018) 33.

  • Karrouchi K, Radi S, Ramli Y, Taoufik J, Mabkhot Y N, Al-aizari F A & Mhammed A, Molecules, 23 (2018) 134.

  • Steinbach G, Lynch P M, Phillips R K S, Wallace M H, Hawk E, Gordon G B, Wakabayashi N, Saunders B, Shen Y, Fujimura T, Su L K, Levin B, Godio L, Patterson S, Rodriguez-Bigas M A, Jester S L, King K L, Schumacher M, Abbruzzese J, DuBois R N, Hittelman W N, Zimmerman S, Sherman J W & Kelloff G, New Eng J Med Chem, 342 (2000) 1946.

  • Uslaner J M, Parmentier-Batteur S, Flick R B, Surles N O, Lam J S H, McNaughton C H, Jacobson M A & Hutson P H, Neuropharmacology, 57 (2009) 531.

  • Gosselin F, O’Shea P D, Webster R A, Reamer R A, Tillyer R D & Grabowski E J J, Synlett, 19 (2006) 3267.

  • Ismail M M F, Khalifa N M, Fahmy H H, EL-Sahrawy H M & Nossier E S, Biomed Res, 27 (2016) 1087.

  • Domínguez J N, Charris J E, Caparelli M & Riggione F, Arzneim Forsch Drug Res, 52 (2002) 482.

  • Bhat M A, Al-Omar M A & Naglah A M, J Enzyme Inhib Med Chem, 33 (2017) 978.

  • Trindade N R, Lopes P R, Naves L M, Fajemiroye J O, Alves P H, AmaralN O, Lião L M, Rebelo A C S, Castro C H, Braga V A, Menegatti R & Pedrino G R , Front Physiol, 9 (2018) 10.

  • Hassan G S, Abdel Rahman D E, Abdelmajeed E A, Refaey R H, Alaraby Salem M, & Nissan Y M, Euro J Med Chem, 171 (2019) 332.

  • Hassan Feid-Allah R S, El Sadany S K & Mohamed H F, J Pharm Sci, 70 (1981) 626.

  • Z. Cimerman, S. Miljanic, and N. Gali; Croatica Chemica Acta, vol. 73, no. 1, pp. 81–95, 2000.

  • H. Schiff; Justus Liebigs Annalen der Chemie, vol. 131, no. 1, pp.

  • –119, 1864.

  • D. N. Dhar and C. L. Taploo; Journal of Scientific and Industrial Research, vol. 41, no. 8, pp. 501–506, 1982.

  • B.S. Sathe, E. Jaychandran, V.A. Jagtap, and G.M. Sreenivasa; International Journal of Pharmaceutical Research and Development, vol. 3, no. 3, pp. 164–169, 2011.

  • S. M. Sondhi, N. Singh, A. Kumar, O. Lozach, and L. Meijer; Bioorganic and Medicinal Chemistry, vol. 14, no. 11, pp. 3758– 3765, 2006.

  • A. Pandey, D. Dewangan, S. Verma, A. Mishra, and R. D. Dubey; International Journal of ChemTech Research, vol. 3, no. 1, pp.178–184, 2011.

  • C. Chandramouli, M. R. Shivanand, T. B. Nayanbhai, B. Bheemachari, and R. H. Udupi, Journal of Chemical and Pharmaceutical Research, vol. 4, no. 2, pp. 1151– 1159, 2012.

  • R. P. Chinnasamy, R. Sundararajan, and S; Govindaraj; Journal of Advanced Pharmaceutical Technology and Research, vol. 1, no. 3, pp. 342–347, 2010.

  • K. Mounika, B. Anupama, J. Pragathi, and C. Gyanakumari; Journal of Scientific Research, vol. 2, no. 3, pp. 513–524, 2010.

  • P. Venkatesh; Asian Journal of Pharmaceutical and Health Sciences, vol. 1, no. 1, pp. 8–11, 2011.

  • A. K. Chaubey and S. N. Pandeya; International Journal of PharmTech Research, vol. 4, no. 4, pp. 590–598, 2012.

  • T. Aboul-Fadl, F. A. Mohammed, and E. A. Hassan; Archives of Pharmacal Research, vol. 26, no. 10, pp. 778–784, 2003.

  • R. Miri, N. Razzaghi-asl, and M. K. Mohammadi; Journal of Molecular Modeling, vol. 19, no. 2, pp. 727–735, 2013.

  • S. M. M. Ali, M. Abul Kalam Azad, M. Jesmin et al.; Asian Pacific Journal of Tropical Biomedicine, vol. 2, no. 6, pp. 438– 442, 2012.

  • D. Wei, N. Li, G. Lu, and K. Yao; Science in China B, vol. 49, no. 3, pp. 225–229, 2006.

  • P. G. Avaji, C. H. Vinod Kumar, S. A. Patil, K. N. Shivananda, and C. Nagaraju; European Journal of Medicinal Chemistry, vol. 44, no. 9, pp. 3552–3559, 2009.

  • S. Li, S. Chen, S. Lei, H. Ma, R. Yu, and D. Liu; Corrosion Science, vol. 41, no. 7, pp. 1273–1287, 1999.

  • A. Kriza, A.Reiss, S.Florea T. Caproiu, J.Ind. Chem.Soc., 77 (2000) 207.

  • L.Bravo, Nutr.Rev., 56 (1998) 317.

  • S.M.Kuo, Crit.Rev.Oncog., 8 (1997) 47


Abstract Views: 127

PDF Views: 0




  • Synthesis Characterization and Antimicrobial Activities of Schiff bases of 3-Formyl chromones

Abstract Views: 127  |  PDF Views: 0

Authors

Ram Vishun Prasad
Assistant Professor, Department of Chemistry, Kisan PG College Babhnan, Gonda, India., India
Ashutosh Singh
Associate Professor, Department of Chemistry, KS Saket PG College Ayodhya, India., India

Abstract


The present paper is all about the synthesis of some novel schiff bases of chromones. The structure conformation of ligand molecule is done by using various spectroscopic techniques such as 1H NMR, IR and elemental analysis. The antibacterial and anti-fungal activities of synthesized complexes were tested according to standard procedure.

Keywords


Schiff base, Chromones, Antibacterial activity, Anti-fungal activity, Pharmacological activity, Condensation, H1NMR, IR, etc.

References