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Volumn 12, Issue , 2015, Pages 6-8

Quinazolinone alkaloids from actinomycete Streptomyces sp. BCC 21795

Author keywords

Actinomycetes; Bioactive secondary metabolites; Quinazolinones; Streptomyces

Indexed keywords

1H INDOLE 3 CARBALDEHYDE; 2 (1H INDOL 3 YL)QUINAZOLIN 4 (3H)ONE; 2 (4 HYDROXYPHENYL) QUINAZOLIN 4 (3H)ONE; 2 ACETAMIDO BENZAMIDE; 2 METHYLQUINAZOLIN 4 (3H)ONE; 2 PHENYLACETAMIDE; 4 PHENYLBUT 3 ENAMIDE; ALKALOID DERIVATIVE; AMPHOTERICIN B; ANTIBIOTIC AGENT; ANTIFUNGAL AGENT; ANTINEOPLASTIC AGENT; DOXORUBICIN; QUINAZOLIN 4 (3H)ONE; QUINAZOLINONE DERIVATIVE; UNCLASSIFIED DRUG; VANCOMYCIN;

EID: 84923584943     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2015.02.007     Document Type: Article
Times cited : (16)

References (24)
  • 3
    • 33847406585 scopus 로고
    • A bronchodilator alkaloid (vasicinone) from Adhatoda vasica Nees
    • A.H. Amin, and D.R. Mehta A bronchodilator alkaloid (vasicinone) from Adhatoda vasica Nees Nature 184 1959 1317
    • (1959) Nature , vol.184 , pp. 1317
    • Amin, A.H.1    Mehta, D.R.2
  • 4
    • 2142712991 scopus 로고    scopus 로고
    • Effect of active synthetic 2-substituted quinazolinones on anti-platelet aggregation and the inhibition of superoxide anion generation by neutrophils
    • F.-R. Chang, C.-C. Wu, T.-L. Hwang, R. Patnam, R.-Y. Kuo, W.-Y. Wang, Y.-H. Lan, and Y.-C. Wu Effect of active synthetic 2-substituted quinazolinones on anti-platelet aggregation and the inhibition of superoxide anion generation by neutrophils Arch. Pharm. Res. 26 2003 511 515
    • (2003) Arch. Pharm. Res. , vol.26 , pp. 511-515
    • Chang, F.-R.1    Wu, C.-C.2    Hwang, T.-L.3    Patnam, R.4    Kuo, R.-Y.5    Wang, W.-Y.6    Lan, Y.-H.7    Wu, Y.-C.8
  • 5
    • 0344443250 scopus 로고    scopus 로고
    • Improved green fluorescent protein reporter gene-based microplate screening for antituberculosis compounds by utilizing an acetamidase promoter
    • C. Changsen, S.G. Franzblau, and P. Palittapongarnpim Improved green fluorescent protein reporter gene-based microplate screening for antituberculosis compounds by utilizing an acetamidase promoter Antimicrob. Agents Chemother. 47 2003 3682 3687
    • (2003) Antimicrob. Agents Chemother. , vol.47 , pp. 3682-3687
    • Changsen, C.1    Franzblau, S.G.2    Palittapongarnpim, P.3
  • 6
    • 0033598323 scopus 로고    scopus 로고
    • Substituted isoquinolines and quinazolines as potential antiinflammatory agents. Synthesis and biological evaluation of inhibitors of tumor necrosis factor α
    • Q. Chao, L. Deng, H. Shih, L.M. Leoni, D. Genini, D.A. Carson, and H.B. Cottam Substituted isoquinolines and quinazolines as potential antiinflammatory agents. Synthesis and biological evaluation of inhibitors of tumor necrosis factor α J. Med. Chem. 42 1999 3860 3873
    • (1999) J. Med. Chem. , vol.42 , pp. 3860-3873
    • Chao, Q.1    Deng, L.2    Shih, H.3    Leoni, L.M.4    Genini, D.5    Carson, D.A.6    Cottam, H.B.7
  • 7
    • 43049128809 scopus 로고    scopus 로고
    • Gallium(III) triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones
    • J. Chen, D. Wu, F. He, M. Liu, H. Wu, J. Ding, and W. Su Gallium(III) triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones Tetrahedron Lett. 49 2008 3814 3818
    • (2008) Tetrahedron Lett. , vol.49 , pp. 3814-3818
    • Chen, J.1    Wu, D.2    He, F.3    Liu, M.4    Wu, H.5    Ding, J.6    Su, W.7
  • 9
    • 0034934409 scopus 로고    scopus 로고
    • Identification and isolation of the cyclooxygenase-2 inhibitory principle in Isatis tinctoria
    • H. Danz, S. Stoyanova, P. Wippich, A. Brattström, and M. Hamburger Identification and isolation of the cyclooxygenase-2 inhibitory principle in Isatis tinctoria Planta Med. 67 2001 411 416
    • (2001) Planta Med. , vol.67 , pp. 411-416
    • Danz, H.1    Stoyanova, S.2    Wippich, P.3    Brattström, A.4    Hamburger, M.5
  • 11
    • 84896964497 scopus 로고    scopus 로고
    • Preparation of one-carbon homologated amides from aldehydes or primary alcohols
    • M.K. Gupta, Z. Li, and T.S. Snowden Preparation of one-carbon homologated amides from aldehydes or primary alcohols Org. Lett. 16 2014 1602 1605
    • (2014) Org. Lett. , vol.16 , pp. 1602-1605
    • Gupta, M.K.1    Li, Z.2    Snowden, T.S.3
  • 12
    • 0025302762 scopus 로고
    • Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization
    • J.B. Jiang, D.P. Hesson, B.A. Dusak, D.L. Dexter, G.J. Kang, and E. Hamel Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization J. Med. Chem. 33 1990 1721 1728
    • (1990) J. Med. Chem. , vol.33 , pp. 1721-1728
    • Jiang, J.B.1    Hesson, D.P.2    Dusak, B.A.3    Dexter, D.L.4    Kang, G.J.5    Hamel, E.6
  • 14
    • 79959861665 scopus 로고    scopus 로고
    • Exploration of antimicrobial and antioxidant potential of newly synthesized 2,3-disubstituted quinazoline-4(3H)-ones
    • A. Kumar, P. Sharma, P. Kumari, and B. Lal Kalal Exploration of antimicrobial and antioxidant potential of newly synthesized 2,3-disubstituted quinazoline-4(3H)-ones Bioorg. Med. Chem. Lett. 21 2011 4353 4357
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 4353-4357
    • Kumar, A.1    Sharma, P.2    Kumari, P.3    Lal Kalal, B.4
  • 15
    • 0345708435 scopus 로고    scopus 로고
    • Newer potential quinazolinones as hypotensive agents
    • A. Kumar, M. Tyagi, and V.K. Srivastava Newer potential quinazolinones as hypotensive agents Indian J. Chem. Sec. B 42B 2003 2142 2145
    • (2003) Indian J. Chem. Sec. B , vol.42 B , pp. 2142-2145
    • Kumar, A.1    Tyagi, M.2    Srivastava, V.K.3
  • 16
    • 84863144304 scopus 로고    scopus 로고
    • Quinazolin-4-one: A highly important hetrocycle with diverse biological activities: A review
    • S. Kumar, G. Mishra, P. Singh, K.K. Jha, R.L. Khosa, and S.K. Gupta Quinazolin-4-one: a highly important hetrocycle with diverse biological activities: a review Der Chem. Sin. 2 2011 36 58
    • (2011) Der Chem. Sin. , vol.2 , pp. 36-58
    • Kumar, S.1    Mishra, G.2    Singh, P.3    Jha, K.K.4    Khosa, R.L.5    Gupta, S.K.6
  • 18
    • 0033856957 scopus 로고    scopus 로고
    • Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity
    • J. O'Brien, I. Wilson, T. Orton, and F. Pongnan Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity Eur. J. Biochem. 267 2000 5421 5426
    • (2000) Eur. J. Biochem. , vol.267 , pp. 5421-5426
    • O'Brien, J.1    Wilson, I.2    Orton, T.3    Pongnan, F.4
  • 20
    • 84877050350 scopus 로고    scopus 로고
    • 3-MCM-41: An efficient magnetic nanocatalyst and recyclable reaction media for the synthesis of quinazolin-4(3H)-one derivatives
    • 3-MCM-41: an efficient magnetic nanocatalyst and recyclable reaction media for the synthesis of quinazolin-4(3H)-one derivatives J. Mol. Catal. A: Chem. 374-375 2013 102 110
    • (2013) J. Mol. Catal. A: Chem. , vol.374-375 , pp. 102-110
    • Rostamizadeh, S.1    Nojavan, M.2    Aryan, R.3    Isapoor, E.4    Azad, M.5
  • 21
    • 84885865579 scopus 로고    scopus 로고
    • Cytotoxic compounds from Laminaria japonica
    • C. Wang, Y. Yang, Z. Mei, and X. Yang Cytotoxic compounds from Laminaria japonica Chem. Nat. Compd. 49 2013 699 701
    • (2013) Chem. Nat. Compd. , vol.49 , pp. 699-701
    • Wang, C.1    Yang, Y.2    Mei, Z.3    Yang, X.4
  • 23
    • 79958727587 scopus 로고    scopus 로고
    • Antifungal quinazolinones from marine-derived Bacillus cereus and their preparation
    • Z. Xu, Y. Zhang, H. Fu, H. Zhong, K. Hong, and W. Zhu Antifungal quinazolinones from marine-derived Bacillus cereus and their preparation Bioorg. Med. Chem. Lett. 21 2011 4005 4007
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 4005-4007
    • Xu, Z.1    Zhang, Y.2    Fu, H.3    Zhong, H.4    Hong, K.5    Zhu, W.6
  • 24
    • 84877033951 scopus 로고    scopus 로고
    • Quinazoline alkaloids from Streptomyces michiganensis
    • J. Xue, L. Xu, Z.-H. Jiang, and X. Wei Quinazoline alkaloids from Streptomyces michiganensis Chem. Nat. Compd. 48 2012 839 841
    • (2012) Chem. Nat. Compd. , vol.48 , pp. 839-841
    • Xue, J.1    Xu, L.2    Jiang, Z.-H.3    Wei, X.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.