메뉴 건너뛰기




Volumn 27, Issue 11, 2004, Pages 1093-1098

Synthesis and antimicrobial activity of certain novel quinoxalines

Author keywords

2 4 (Ethoxycarbonyl) anilino 3 methylquinoxaline; Antimicrobial agents; Oxadiazoiyl quinoxalines

Indexed keywords

ANTIINFECTIVE AGENT; QUINOXALINE DERIVATIVE;

EID: 16644389614     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/BF02975110     Document Type: Article
Times cited : (118)

References (17)
  • 1
    • 0042286626 scopus 로고    scopus 로고
    • Synthesis of certain substituted quinoxalines as antimicrobial agents. Part II
    • PID: 12643584, COI: 1:CAS:528:DC%2BD3sXitlCru7o%3D
    • Badran, M. M., Abouzid, K. A. M., and Hussein, M. H. M., Synthesis of certain substituted quinoxalines as antimicrobial agents. Part II.Arch. Pharm. Res., 26, 107–113 (2003). DOI: 10.1007/BF02976653
    • (2003) Arch. Pharm. Res. , vol.26 , pp. 107-113
    • Badran, M.M.1    Abouzid, K.A.M.2    Hussein, M.H.M.3
  • 3
    • 34248672644 scopus 로고
    • Synthetic antimalerials. Part. XXXIX Dialkylaminoalkylamino quinoxalines
    • Crowther, A. F., Curd, F. H. S., Davey, D. G., and Stacey, G. J., Synthetic antimalerials. Part. XXXIX Dialkylaminoalkylamino quinoxalines.J. Chem. Soc., 1260–1262 (1949).
    • (1949) J. Chem. Soc. , pp. 1260-1262
    • Crowther, A.F.1    Curd, F.H.S.2    Davey, D.G.3    Stacey, G.J.4
  • 4
    • 0018139986 scopus 로고
    • Synthesis and antibacterial Activity of Isomeric 6-and 7-acetyl-3-methyl-2-quinoxaline-carboxamide 1,4-dioxides
    • PID: 660596, COI: 1:CAS:528:DyaE1cXhsVKhtLs%3D
    • Dirlam, J. P. and Presslitz, J. E., Synthesis and antibacterial Activity of Isomeric 6-and 7-acetyl-3-methyl-2-quinoxaline-carboxamide 1,4-dioxides.J. Med. Chem., 21, 483–485 (1978). DOI: 10.1021/jm00203a017
    • (1978) J. Med. Chem. , vol.21 , pp. 483-485
    • Dirlam, J.P.1    Presslitz, J.E.2
  • 5
    • 0028846491 scopus 로고
    • Synthesis of some quinoxaline derivatives containing indoline-2,3-dione or thiazolidine residue as potential antimicrobial agents
    • COI: 1:CAS:528:DyaK2MXmvVyrsLk%3D
    • El-Gendy, A. A., El-Meligie, S., El-Ansary, A., and Ahmedy, A. M., Synthesis of some quinoxaline derivatives containing indoline-2,3-dione or thiazolidine residue as potential antimicrobial agents.Arch. Pharm. Res., 18, 44–47 (1995). DOI: 10.1007/BF02976507
    • (1995) Arch. Pharm. Res. , vol.18 , pp. 44-47
    • El-Gendy, A.A.1    El-Meligie, S.2    El-Ansary, A.3    Ahmedy, A.M.4
  • 6
    • 0032733071 scopus 로고    scopus 로고
    • Quinoxaline derivatives Part II: synthesis and antimicrobial testing of 1,2, 4-triazolo[4,3-a]quinoxalines, 1,2,4-triazino[4,3-a]quinoxalines and 2-pyrazolylquinoxalines
    • PID: 10603606, COI: 1:CAS:528:DyaK1MXnslOjsbc%3D
    • El-Hawash, S. A., Habib, N. S., and Fanaki, N. H., Quinoxaline derivatives Part II: synthesis and antimicrobial testing of 1,2, 4-triazolo[4,3-a]quinoxalines, 1,2,4-triazino[4,3-a]quinoxalines and 2-pyrazolylquinoxalines.Pharmazie, 54, 808–815 (1999).
    • (1999) Pharmazie , vol.54 , pp. 808-815
    • El-Hawash, S.A.1    Habib, N.S.2    Fanaki, N.H.3
  • 7
    • 3242819850 scopus 로고
    • Synthesis and characterization of 1,2,4-triazolo[4,3-a]quinoxalines and 1,2,4-triazolo-s-triazines as potential antimicrobial agent
    • COI: 1:CAS:528:DyaK38XlvFehtw%3D%3D
    • El-Kerdawy, M., Tantawy, A., Gad, L. M., and Rady, E., Synthesis and characterization of 1,2,4-triazolo[4,3-a]quinoxalines and 1,2,4-triazolo-s-triazines as potential antimicrobial agent.Zhonghua yaoxue zazhi, 43, 355–364 (1991).
    • (1991) Zhonghua yaoxue zazhi , vol.43 , pp. 355-364
    • El-Kerdawy, M.1    Tantawy, A.2    Gad, L.M.3    Rady, E.4
  • 8
    • 0009834369 scopus 로고
    • Inhibition of glucosamine-6-phosphate synthase from Candida albicans by quinoxaline-2,3-diones
    • COI: 1:CAS:528:DyaK3sXhvVarsLY%3D
    • Griffith, R. K., Chittur, S. V., and Chen, Y. C., Inhibition of glucosamine-6-phosphate synthase from Candida albicans by quinoxaline-2,3-diones.Med. Chem. Res., 2, 467–473 (1992).
    • (1992) Med. Chem. Res. , vol.2 , pp. 467-473
    • Griffith, R.K.1    Chittur, S.V.2    Chen, Y.C.3
  • 9
    • 0022981623 scopus 로고
    • Synthesis of 3-(α-chlorophenylhydrazono) heteroarylmethyl-2-oxo-1,2-dihydroquinoxalines with antimicrobial activity [I]
    • COI: 1:CAS:528:DyaL1cXjslOrsg%3D%3D
    • Kurasawa, Y. Muramatsu, M., Yamazaki, K., Okamoto, Y., and Takade, A., Synthesis of 3-(α-chlorophenylhydrazono) heteroarylmethyl-2-oxo-1,2-dihydroquinoxalines with antimicrobial activity [I].J. Heterocyclic Chem., 23, 1387- 1390 (1986a). DOI: 10.1002/jhet.5570230526
    • (1986) J. Heterocyclic Chem. , vol.23 , pp. 1387- 1390
    • Kurasawa, Y.1    Muramatsu, M.2    Yamazaki, K.3    Okamoto, Y.4    Takade, A.5
  • 10
    • 84986435676 scopus 로고
    • A Facile synthesis of 1-aryl-3- heteroaryl-1H-pyrazolo[3,4-b]quinoxalines and related compounds with antifungal activity [I]
    • COI: 1:CAS:528:DyaL1cXitFygtA%3D%3D
    • Kurasawa, Y., Muramatsu, M., Yamazaki, K., Tajima, S., Okamoto, Y., and Takada, A., A Facile synthesis of 1-aryl-3- heteroaryl-1H-pyrazolo[3,4-b]quinoxalines and related compounds with antifungal activity [I].J. Heterocyclic Chem., 23, 1391–1394 (1986b).
    • (1986) J. Heterocyclic Chem. , vol.23 , pp. 1391-1394
    • Kurasawa, Y.1    Muramatsu, M.2    Yamazaki, K.3    Tajima, S.4    Okamoto, Y.5    Takada, A.6
  • 11
    • 10544251444 scopus 로고    scopus 로고
    • High affinity a-aminobutyric acid A/ Benzo diazepine ligands: Synthesis and structure-activity relationship. Studies of a new series of tertracyclic imidazoquinoxalines
    • PID: 8917654, COI: 1:CAS:528:DyaK28Xmt1ylsLw%3D
    • Mickelson, J. W., Jacobsen, E. J., Carter, D. B., Im, H. K., Im, W. B., Schreur, P. J. K. D., Sethy, V. H., Tang., A. H., McGee, J. E., and Petke, J. D., High affinity a-aminobutyric acid A/ Benzo diazepine ligands: Synthesis and structure-activity relationship. Studies of a new series of tertracyclic imidazoquinoxalines.J. Med. Chem., 39, 4654–4666 (1996). DOI: 10.1021/jm960401i
    • (1996) J. Med. Chem. , vol.39 , pp. 4654-4666
    • Mickelson, J.W.1    Jacobsen, E.J.2    Carter, D.B.3    Im, H.K.4    Im, W.B.5    Schreur, P.J.K.D.6    Sethy, V.H.7    Tang, A.H.8    McGee, J.E.9    Petke, J.D.10
  • 14
    • 0025306964 scopus 로고
    • 4-Amino[1,2,4]triazolo [4,3-a] quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants
    • PID: 2374150, COI: 1:CAS:528:DyaK3cXksF2is74%3D
    • Sarges, R., Howard, H. R., Browne, R. G., Lebel, L. A., Seymour, P. A., and Koe, B. K., 4-Amino[1,2,4]triazolo [4,3-a] quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants.J. Med. Chem., 33, 2240–2254 (1990). DOI: 10.1021/jm00170a031
    • (1990) J. Med. Chem. , vol.33 , pp. 2240-2254
    • Sarges, R.1    Howard, H.R.2    Browne, R.G.3    Lebel, L.A.4    Seymour, P.A.5    Koe, B.K.6
  • 15
    • 0344815145 scopus 로고
    • Studies on compounds related to pyrazine. II. The reaction of 3-substituted-2-hydrazinoqu-inoxalines with carbonyl compounds
    • COI: 1:CAS:528:DyaF38Xns12q
    • Shiho, D. and Tagami, S., Studies on compounds related to pyrazine. II. The reaction of 3-substituted-2-hydrazinoqu-inoxalines with carbonyl compounds.J. Am. Chem. Soc, 82, 4044–4054 (1960). DOI: 10.1021/ja01500a058
    • (1960) J. Am. Chem. Soc , vol.82 , pp. 4044-4054
    • Shiho, D.1    Tagami, S.2
  • 16
    • 0028314652 scopus 로고
    • Antagonist, Partial agonist and full agonist imidazo[1,5- a] quinoxaline amides and carbamates acting through the GABA/Benzodiazepine receptor
    • PID: 8145225, COI: 1:CAS:528:DyaK2cXktlGmsbs%3D
    • TenBrink, R. E., Im, W. B., Sethy, V. H., Tang, A. H., and Carter, D. B., Antagonist, Partial agonist and full agonist imidazo[1,5- a] quinoxaline amides and carbamates acting through the GABA/Benzodiazepine receptor.J. Med. Chem., 37, 758- 768 (1994). DOI: 10.1021/jm00032a008
    • (1994) J. Med. Chem. , vol.37 , pp. 758- 768
    • TenBrink, R.E.1    Im, W.B.2    Sethy, V.H.3    Tang, A.H.4    Carter, D.B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.