“Anti-microbial Study and Synthesis of Schiff bases of 3-actyl 4-hydroxy Quinolin-2-one”
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Published:2023-02-28
Issue:1
Volume:39
Page:197-201
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ISSN:2231-5039
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Container-title:Oriental Journal Of Chemistry
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language:en
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Short-container-title:Orient. J. Chem
Author:
Anjanikar Shivraj S.1ORCID, Chandole Santosh S.2ORCID
Affiliation:
1. 1Department of Chemistry, Sharadchandra College, Naigaon, District- Nanded MS- 431709, India. 2. 2Department of Chemistry, S.G.B. College, Purna Jn., MS- 431511, India, (Affilated to Swami Ramanand Teerth Marathwada University, Nanded) India.
Abstract
Quinoline based new Schiff bases were synthesized from 3-Actyl 4-Hydroxy Quinolin-2-(1H)-one and screened their antibacterial and antifungal activity. The Schiff bases 4-hydroxy-3-(1-((4-picolin-2-yl)imino)ethyl)quinolin-2-(1H)-one(L1),4-hydroxy-3-(1-((5-picolin-2-yl)imino)ethyl)quinolin-2(1H)-one(L2),4-hydroxy-3-(1-((6-picolin-2-yl)-imino)ethyl)quinolin-2(1H)-one(L3) and 4-hydroxy-3-(1-((3-nitro-4-picolin-2-yl)imino)ethyl)quinolin-2-(1H)-one (L4) were preparedfrom 3-Acetyl 4-Hydroxy Quinolin-2-One with 2-amino picolines. The structures of Schiff bases were confirmed by Infrared, mass, proton-NMR and 13CNMR spectral analysis. In vitro studies of these Schiff bases were carried out for their antibacterial activity by Agar contact method and antifungal activity by the poison plate method. The bacterial species used were B. subtilis, E. coli, S. typhi, and S. aureus. Fungal species used were F. moneliforme, A.niger, A. flavus, and P. chrysogenum.
Publisher
Oriental Scientific Publishing Company
Subject
Drug Discovery,Environmental Chemistry,Biochemistry,General Chemistry
Reference34 articles.
1. 1. Shang X.F., Morris-Natschke S.L.,Liu Y.Q., Guo X., Xu X.S.,Goto M., Li J.C., Yang G.Z., and Lee K.H., Medicinal Research Reviews, 2018, (38)3, 775–828. 2. 2. Shang X.F., Morris-Natschke S.L., Susan L.L.; Yang G.Z., Liu Y.Q., Guo X., Xu X.S., Goto M., Masuo L.; Li J.C., Zhang J.Y., and Lee.K.H., Medicinal Research Reviews. 2018, (38)5, 1614–1660. 3. 3. Nazrullaev S.S., Bessonova I.A., Akhmedkhodzhaeva K.S., Chem. Nat. Compd., 2001, (37)6, 551-555. 4. 4. Barreca M.L., Manfroni G., Leyssen P., Winquist J., Kaushik-Basu N., Paeshuyse J., Krishnan R., Iraci N., Sabatini S., Tabarrini O., Basu A., Danielson U.H.,Neyts J., Cecchetti V., J. Med. Chem., 2013, (56)6, 2270-2282. 5. 5. Vicente J. de, Hendricks R.T., Smith D.B., Fell J.B., Fischer J., Spencer S.R., P.J., Stengel P. Mohr, RobinsonJ.E., Blake J.F., Hilgenkamp R.K., Yee C., Adjabeng G., Elworthy T.R., Tracy J., Chin E., Li J., Wang B., Bamberg J.T., Stephenson R., Oshiro C., Harris S.F., Ghate M., Leveque V.,Najera I., Le Pogam S., Rajyaguru S., Ao-Ieong G., Alexandrova L., Larrabee S., Brandl M., Briggs A., Sukhtankar S., Farrell R., Xu B.., Bioorg. Med. Chem. Lett., 2009, (19)13, 3642-3646,.
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