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Volumn , Issue 1, 2009, Pages 163-169

Synthesis and antibacterial activity of quinazolinone derivatives

Author keywords

Antibacterial activity; Quinazolinone derivatives

Indexed keywords

2 (4 NITROPHENOXY) N [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]ACETAMIDE; 2 CHLORO N [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]ACETAMIDE; ACETAMIDE DERIVATIVE; ACETONE; AMPICILLIN; ANTIINFECTIVE AGENT; PHENOL DERIVATIVE; POTASSIUM CARBONATE; POTASSIUM IODIDE; QUINAZOLINE DERIVATIVE; QUINAZOLINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77953467230     PISSN: None     EISSN: 09751491     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (20)

References (8)
  • 1
    • 33845625595 scopus 로고    scopus 로고
    • Synthesis, insecticidal and antimicrobial activities of some heterocyclic derivatives of quinazolinone
    • Tripti Singh, Shalabh Sharma, Virendra Kishore Srivastava & Ashok Kumar. Synthesis, insecticidal and antimicrobial activities of some heterocyclic derivatives of quinazolinone, Indian Journal of Chemistry 2006; 45B: 2558-2565.
    • (2006) Indian Journal of Chemistry , vol.45 B , pp. 2558-2565
    • Singh, T.1    Sharma, S.2    Kishore Srivastava, V.3    Kumar, A.4
  • 2
    • 0642378328 scopus 로고    scopus 로고
    • Synthesis, Analgesic and Anti-inflammatory Activities of Some Novel 2,3-Disubstituted Quinazolin-4 (3H)-ones
    • Veerachamy Alagarsamy, Veluchamy Muthukumar, Nagendran Pavalarani, Poongavanam Vasanthanathan, and Rajappan Revathi. Synthesis, Analgesic and Anti-inflammatory Activities of Some Novel 2,3-Disubstituted Quinazolin-4 (3H)-ones, Biol. Pharm. Bull.2003; 26(4): 557-559.
    • (2003) Biol. Pharm. Bull , vol.26 , Issue.4 , pp. 557-559
    • Alagarsamy, V.1    Muthukumar, V.2    Pavalarani, N.3    Vasanthanathan, P.4    Revathi, R.5
  • 3
    • 33745542076 scopus 로고    scopus 로고
    • Synthesis and Antifungal Bioactivities of 3-Alkylquinazolin-4-one Derivatives
    • Guiping Ouyang, Peiquan Zhang, Gangfang Xu, Baoan Song, Song Yang, Linhong Jin, Wei Xue, Deyu Hu, Ping Lu and Zhuo Chen. Synthesis and Antifungal Bioactivities of 3-Alkylquinazolin-4-one Derivatives, Molecules 2006; 11: 383-392.
    • (2006) Molecules , vol.11 , pp. 383-392
    • Ouyang, G.1    Zhang, P.2    Xu, G.3    Song, B.4    Yang, S.5    Jin, L.6    Xue, W.7    Hu, D.8    Lu, P.9    Chen, Z.10
  • 4
    • 35948973607 scopus 로고    scopus 로고
    • Ashis Kumar Nanda, Subarna Ganguli and Ranadhir Chakraborty. Antibacterial Activity of Some 3-(Arylideneamino)-2-phenylquinazoline-4(3H)- ones: Synthesis and Preliminary QSAR Studies, Molecules 2007; 12: 2413-2426.
    • Ashis Kumar Nanda, Subarna Ganguli and Ranadhir Chakraborty. Antibacterial Activity of Some 3-(Arylideneamino)-2-phenylquinazoline-4(3H)- ones: Synthesis and Preliminary QSAR Studies, Molecules 2007; 12: 2413-2426.
  • 6
    • 38149104561 scopus 로고    scopus 로고
    • Synthesis and Antiviral Bioactivities of 2-Aryl- or 2-Methyl-3-(substituted- Benzalamino)-4(3H)-quinazolinone Derivatives
    • Xingwen Gao, Xuejian Cai, Kai Yan, Baoan Song, Lili Gao and Zhuo Chen. Synthesis and Antiviral Bioactivities of 2-Aryl- or 2-Methyl-3-(substituted- Benzalamino)-4(3H)-quinazolinone Derivatives, Molecules 2007; 12: 2621-2642.
    • (2007) Molecules , vol.12 , pp. 2621-2642
    • Gao, X.1    Cai, X.2    Yan, K.3    Song, B.4    Gao, L.5    Chen, Z.6
  • 7
    • 77953396517 scopus 로고    scopus 로고
    • Indian Pharmacopoeia. 3rd ed. The controller of publications, Delhi; 1996. p. 105-107.
    • Indian Pharmacopoeia. 3rd ed. The controller of publications, Delhi; 1996. p. 105-107.
  • 8
    • 33644944329 scopus 로고    scopus 로고
    • Synthesis and evaluation of new quinazolone derivatives of nalidixic acid as potential antibacterial and antifungal agents
    • Gaurav Grover, Suvarna G. Kini. Synthesis and evaluation of new quinazolone derivatives of nalidixic acid as potential antibacterial and antifungal agents, European Journal of Medicinal Chemistry 2006; 41: 256-262.
    • (2006) European Journal of Medicinal Chemistry , vol.41 , pp. 256-262
    • Grover, G.1    Kini, S.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.