메뉴 건너뛰기




Volumn 21, Issue 7, 2012, Pages 1199-1206

Synthesis, characterization, and antimicrobial studies of novel 1,3,4-thiadiazolium-5-thiolates

Author keywords

1,3,4 Thiadiazolium 5 thiolate; Antibacterial activity; Mesoionic; Quinazoline

Indexed keywords

1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (2 CHLORO 5 NITROPHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (3 NITROPHENYL) 3 [4 [(2 PHENYL 4 QUINAZOLINYL)AMINO]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (3 NITROPHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3 (4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 CHLORO 3 NITROPHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3 (4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 CHLOROPHENYL) 3 [4 [(2 PHENYL 4 QUINAZOLINYL)AMINO]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 CHLOROPHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3 (4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 METHOXY 3 NITROPHENYL) 3 [4 [(2 PHENYL 4 QUINAZOLINYL)AMINO]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 METHOXY 3 NITROPHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3 (4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 NITROPHENYL) 3 [4 [(2 PHENYL 4 QUINAZOLINYL)AMINO]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (4 NITROPHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3 (4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (METHYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (PHENYL) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 (SUBSTITUTED) 3 [4 [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 [[4 (4 OXO 2 PHENYLQUINAZOLINE 3(4H) YL] PHENYL]CARBONYL]HYDRAZINE CARBODITHIOIC ACID; 2 [[4 [4 OXO 2 PHENYLQUINAZOLINE 3(4H) YL] PHENYL]CARBONYL]HYDRAZINE CARBODITHIOIC ACID; 2 METHYL 3 [4 [(2 PHENYL 4 QUINAZOLINYL)AMINO]BENZOYL]1,3,4 THIADIAZOLIUM 5 THIOLATE; 2 METHYL 3 O TOLYL 4 (3H) QUINAZOLINONE; 2 PHENYLQUINAZOLIN 4(3H) ONE; 2 SUBSTITUTED 3 [4 [(2 PHENYL 4 QUINAZOLINYL)AMINO]BENZOYL] 1,3,4 THIADIAZOLIUM 5 THIOLATE; 4 [(2 PHENYL 3,4 DIHYDROQUINAZOLIN 4 YL)AMINO]BENZOHYDRAZIDE; 4 [(2 PHENYL 3,4 DIHYDROQUINAZOLIN 4 YL)AMINO]BENZOIC ACID; 4 [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]BENZOHYDRAZIDE; 4 [4 OXO 2 PHENYLQUINAZOLIN 3(4H) YL]BENZOIC ACID; 4 CHLORO 2 PHENYL 3,4 DIHYDROQUINAZOLINE; ANTHRANILIC ACID; ANTIINFECTIVE AGENT; QUINAZOLINE DERIVATIVE; THIADIAZOLE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84861890736     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-011-9632-2     Document Type: Article
Times cited : (20)

References (14)
  • 1
    • 0030450411 scopus 로고    scopus 로고
    • Studies on disease-modifying antirheumatic drugs: Synthesis of novel quinoline and quinazoline derivatives and their anti-inflammatory effect
    • Baba A, Kawamura N, Makino H, Ohta Y, Taketomi S, Sohda T (1996) Studies on disease-modifying antirheumatic drugs: synthesis of novel quinoline and quinazoline derivatives and their anti-inflammatory effect. J Med Chem 39:5176-5182
    • (1996) J Med Chem , vol.39 , pp. 5176-5182
    • Baba, A.1    Kawamura, N.2    Makino, H.3    Ohta, Y.4    Taketomi, S.5    Sohda, T.6
  • 2
    • 70350749082 scopus 로고    scopus 로고
    • Mesoionic compounds: An unconventional class of aromatic heterocycles
    • Badami BV (2006) Mesoionic compounds: an unconventional class of aromatic heterocycles. Resonance 11:40-48
    • (2006) Resonance , vol.11 , pp. 40-48
    • Badami, B.V.1
  • 3
    • 4544342467 scopus 로고    scopus 로고
    • Synthesis and biological activity of novel antibacterial quinazolines
    • Bedi PMS, Kumar V, Mahajan MP (2004) Synthesis and biological activity of novel antibacterial quinazolines. Bioorg Med Chem Lett 14:5211-5213
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 5211-5213
    • Pms, B.1    Kumar, V.2    Mahajan, M.P.3
  • 4
    • 1342279612 scopus 로고    scopus 로고
    • Structure-activity relationship study of antimalarial indolo [2,1-b]quinazoline-6,12-diones (tryptanthrins). Three dimensional pharmacophore modeling and identification of new antimalarial candidates
    • Bhattacharjee AK, Hartell MG, Nichols DA, Hicks RP, Stanton B, van Hamont JE, Milhous WA (2004) Structure-activity relationship study of antimalarial indolo [2,1-b]quinazoline-6,12-diones (tryptanthrins). Three dimensional pharmacophore modeling and identification of new antimalarial candidates. Eur J Med Chem 39:59-67
    • (2004) Eur J Med Chem , vol.39 , pp. 59-67
    • Bhattacharjee, A.K.1    Hartell, M.G.2    Nichols, D.A.3    Hicks, R.P.4    Stanton, B.5    Van Hamont, J.E.6    Milhous, W.A.7
  • 5
    • 67651117729 scopus 로고
    • Studies with the agar cup-plate method I. A standardized agar cup-plate technique
    • Brandt Rose S, Miller RE (1939) Studies with the agar cup-plate method I. A standardized agar cup-plate technique. J Bacteriol 38(5):525-537
    • (1939) J Bacteriol , vol.38 , Issue.5 , pp. 525-537
    • Brandt Rose, S.1    Miller, R.E.2
  • 7
    • 0016196782 scopus 로고
    • Potential antileprotic agents. 3. Inhibition of mycobacterial dihydrofolic reductase by 2,4-diamino-5-methyl-6-alkylquinazolines
    • DeGraw JI, Brown GH, Colwell WT (1974) Potential antileprotic agents. 3. Inhibition of mycobacterial dihydrofolic reductase by 2,4-diamino-5-methyl-6- alkylquinazolines. J Med Chem 17: 762-764
    • (1974) J Med Chem , vol.17 , pp. 762-764
    • De Graw, J.I.1    Brown, G.H.2    Colwell, W.T.3
  • 8
    • 19944393889 scopus 로고    scopus 로고
    • Niementowski reaction: Microwave induced and conventional synthesis of quinazolinones and 3-methyl-1H-5-pyrazolones and their antimicrobial activity
    • Desai AR, Desai KR (2005) Niementowski reaction: microwave induced and conventional synthesis of quinazolinones and 3-methyl-1H-5-pyrazolones and their antimicrobial activity. Arkivoc 13:98-108
    • (2005) Arkivoc , vol.13 , pp. 98-108
    • Desai, A.R.1    Desai, K.R.2
  • 9
    • 0032434409 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of some non-nucleoside 2,3-disubstituted quinazoline derivatives (Part-V)
    • Desai NC, Undavia NK, Trivedi PB, Dave D, Vyas GD (1998) Synthesis and anti-HIV activity of some non-nucleoside 2,3-disubstituted quinazoline derivatives (Part-V). Indian J Exp Biol 36:1280-1283
    • (1998) Indian J Exp Biol , vol.36 , pp. 1280-1283
    • Desai, N.C.1    Undavia, N.K.2    Trivedi, P.B.3    Dave, D.4    Vyas, G.D.5
  • 10
    • 51449107911 scopus 로고    scopus 로고
    • Biological evaluation of novel 6-arylbenzimidazo [1,2-c]quinazoline derivatives as inhibitors of LPS-induced TNF-alpha secretion
    • Galarce GD, Foncea RE, Edwards AM, Pessoa-mahana H, Pessoamahana CD, Ebensperger RA (2008) Biological evaluation of novel 6-arylbenzimidazo [1,2-c]quinazoline derivatives as inhibitors of LPS-induced TNF-alpha secretion. Biol Res 41:43-50
    • (2008) Biol Res , vol.41 , pp. 43-50
    • Galarce, G.D.1    Foncea, R.E.2    Edwards, A.M.3    Pessoa-Mahana, H.4    Pessoamahana, C.D.5    Ebensperger, R.A.6
  • 11
    • 62649102716 scopus 로고    scopus 로고
    • Transition metal complexes of a potential anticancer quinazoline ligand
    • Gudasi KB, Patil SA, Kulkarni MV, Nethaji M (2009) Transition metal complexes of a potential anticancer quinazoline ligand. Trans Met Chem 34(3):325-330
    • (2009) Trans Met Chem , vol.34 , Issue.3 , pp. 325-330
    • Gudasi, K.B.1    Patil, S.A.2    Kulkarni, M.V.3    Nethaji, M.4
  • 12
    • 77954083642 scopus 로고    scopus 로고
    • Anticonvulsant and sedative-hypnotic activity of some novel 3-[5-(4-substituted) phenyl-1,3,4-oxadiazole-2yl] -2-styrylquinazoline-4(3H)- ones
    • Kashaw SK, Gupta V, Kashaw V, Mishra P, Stables JP, Jain NK (2010) Anticonvulsant and sedative-hypnotic activity of some novel 3-[5-(4-substituted) phenyl-1,3,4-oxadiazole-2yl]-2-styrylquinazoline-4(3H)-ones. Med Chem Res 19:250-261
    • (2010) Med Chem Res , vol.19 , pp. 250-261
    • Kashaw, S.K.1    Gupta, V.2    Kashaw, V.3    Mishra, P.4    Stables, J.P.5    Jain, N.K.6
  • 13
    • 0000479718 scopus 로고
    • An alkaloid with high antimalarial activity from Dichroa febrifuga
    • Koepfli JB, Mead JF, Brockman JA Jr (1947) An alkaloid with high antimalarial activity from Dichroa febrifuga. J Am Chem Soc 69:1837
    • (1947) J Am Chem Soc , vol.69 , pp. 1837
    • Koepfli, J.B.1    Mead, J.F.2    Brockman Jr., J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.