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Volumn 59, Issue 4, 2004, Pages 243-250

Pyrido[3,2-b]indol-4-yl-amines - Synthesis and investigation of activity against malaria;Pyrido[3,2-b]indol-4-yl-amine - Synthese und prüfung auf wirksamkeit gegen malaria

Author keywords

[No Author keywords available]

Indexed keywords

4 [4 HYDROXY 3,5 BIS(PYRROLIDINOMETHYL)PHENYLAMINO] 5H PYRIDO[3,2 B]INDOL 3 CARBONIC ACID ETHYL ESTER; 4 CHLOROPYRIDINE DERIVATIVE; AMODIAQUINE DERIVATIVE; ANTIMALARIAL AGENT; CHLOROQUINE; INDOLE DERIVATIVE; MANNICH BASE; NOVALDIAME; PHENOL DERIVATIVE; PYRIDINE DERIVATIVE; PYRIDO[3,2 B]INDOL 4 YLAMINE DERIVATIVE; PYRIDO[3,2 B]INDOLE; UNCLASSIFIED DRUG;

EID: 1842862809     PISSN: 00317144     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (18)

References (21)
  • 1
    • 0032519825 scopus 로고    scopus 로고
    • Antimalarial activity of 77 phospholipid polar head analogs: Close correlation between inhibition of phospholipid metabolism and in vitro Plasmodium falciparum growth
    • Ancelin ML, Calas M, Bompart J, Cordina G, Martin D, Ben Bari M, Jei T, Druilhe P, Vial HJ (1998) Antimalarial activity of 77 phospholipid polar head analogs: close correlation between inhibition of phospholipid metabolism and in vitro Plasmodium falciparum growth. Blood 91: 1426-1437.
    • (1998) Blood , vol.91 , pp. 1426-1437
    • Ancelin, M.L.1    Calas, M.2    Bompart, J.3    Cordina, G.4    Martin, D.5    Ben Bari, M.6    Jei, T.7    Druilhe, P.8    Vial, H.J.9
  • 2
    • 1842350408 scopus 로고
    • Antimalariamittel aus der Gruppe halogensubstituierter Chinolinverbindungen
    • Andersag H (1948) Antimalariamittel aus der Gruppe halogensubstituierter Chinolinverbindungen. Chem Ber 81: 499-507.
    • (1948) Chem Ber , vol.81 , pp. 499-507
    • Andersag, H.1
  • 3
    • 33947445299 scopus 로고
    • Aminoalkylphenols as Antimalarials. II (Heterocyclic-amino)-á -amino-o-cresols. The Synthesis of Camoquin
    • Burckhalter JH, Tendick FH, Jones EM, Jones PA, Holcomb WF, Rawlins AL (1948) Aminoalkylphenols as Antimalarials. II (Heterocyclic-amino)-á -amino-o-cresols. The Synthesis of Camoquin. J Am Chem Soc 70: 1363-1373.
    • (1948) J Am Chem Soc , vol.70 , pp. 1363-1373
    • Burckhalter, J.H.1    Tendick, F.H.2    Jones, E.M.3    Jones, P.A.4    Holcomb, W.F.5    Rawlins, A.L.6
  • 5
    • 1842848218 scopus 로고    scopus 로고
    • Boyarintseva ON, Kurilo GN, Anisimova OS, Grinev AN (1977) Reaction of 3-aminoindole-2-carboxylic acids with an acetylenedicarboxylate ester. Khim Geterotsikl Soedin: 82-84; CA 86: 189761p.
    • CA , vol.86
  • 6
    • 0018606732 scopus 로고
    • Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
    • Desjardins RE, Canfield CJ, Haynes JD, Chulay JD (1979) Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique. Antimicrob Agents Chemother 16: 710-718.
    • (1979) Antimicrob Agents Chemother , vol.16 , pp. 710-718
    • Desjardins, R.E.1    Canfield, C.J.2    Haynes, J.D.3    Chulay, J.D.4
  • 7
    • 0028336639 scopus 로고
    • Gegen Malaria wirksame 10H-Indolo[3,2-b]chinoline-11-yl-amine, 1. Mitt.: Phenol-Mannich-Basen vom Amodiaquin- und Cycloquin-Typ
    • Görlitzer K, Stockmann R, Walter RD (1994) Gegen Malaria wirksame 10H-Indolo[3,2-b]chinoline-11-yl-amine, 1. Mitt.: Phenol-Mannich-Basen vom Amodiaquin- und Cycloquin-Typ. Pharmazie 49: 231-235.
    • (1994) Pharmazie , vol.49 , pp. 231-235
    • Görlitzer, K.1    Stockmann, R.2    Walter, R.D.3
  • 8
    • 0028887767 scopus 로고
    • Gegen Malaria wirksame 10H-Indolo[3,2-b]chinoline-11-yl-amine, 2. Mitt.: Chloroquin-Analoge
    • Görlitzer K, Stockmann R, Walter RD (1995) Gegen Malaria wirksame 10H-Indolo[3,2-b]chinoline-11-yl-amine, 2. Mitt.: Chloroquin-Analoge. Pharmazie 50: 105-111.
    • (1995) Pharmazie , vol.50 , pp. 105-111
    • Görlitzer, K.1    Stockmann, R.2    Walter, R.D.3
  • 11
    • 0033625196 scopus 로고    scopus 로고
    • Reaktionen von 4,5-Dihydro-4-oxo-1H-pyrido[3,2-b]indol-2-carbonsä urestern
    • Görlitzer K, Kramer C (2000) Reaktionen von 4,5-Dihydro-4-oxo-1H-pyrido[3,2-b]indol-2-carbonsäurestern. Pharmazie 55: 273-281.
    • (2000) Pharmazie , vol.55 , pp. 273-281
    • Görlitzer, K.1    Kramer, C.2
  • 12
    • 0029817144 scopus 로고    scopus 로고
    • Manipulation of the N-alkyl substituent in amodiaquine to overcome the verapamil-sensitive chloroquine resistance component
    • Hawley SRR, Bray PG, O'Neill PM, Naisbitt DJ, Park BK, Ward S (1996) Manipulation of the N-alkyl substituent in amodiaquine to overcome the verapamil-sensitive chloroquine resistance component. Antimicrob Agents Chemother 40: 2345-2349.
    • (1996) Antimicrob Agents Chemother , vol.40 , pp. 2345-2349
    • Hawley, S.R.R.1    Bray, P.G.2    O'Neill, P.M.3    Naisbitt, D.J.4    Park, B.K.5    Ward, S.6
  • 13
    • 0001260775 scopus 로고
    • Investigation of two radical intermediates in the anodic oxidation of 1,4-dihydropyridines by electrochemiluminescence
    • Ludvik J, Volke J, Pragst F (1986) Investigation of two radical intermediates in the anodic oxidation of 1,4-dihydropyridines by electrochemiluminescence. J Electroanal Chem 215: 179-190.
    • (1986) J Electroanal Chem , vol.215 , pp. 179-190
    • Ludvik, J.1    Volke, J.2    Pragst, F.3
  • 14
    • 0000512068 scopus 로고
    • Electrochemical oxidation mechanisms of different type 1,4-Dihydropyridine derivatives in acetonitrile
    • Ludvik J, Volke J, Klima J (1987) Electrochemical oxidation mechanisms of different type 1,4-Dihydropyridine derivatives in acetonitrile. Electrochim Acta 32: 1063-1071.
    • (1987) Electrochim Acta , vol.32 , pp. 1063-1071
    • Ludvik, J.1    Volke, J.2    Klima, J.3
  • 15
    • 0010208757 scopus 로고
    • (1976) Pyridonecarboxylic acid derivatives. Japan. Kokai 76.136.698
    • Minami S, Yamabe S, Sakurai H, Hirose T (1976) Pyridonecarboxylic acid derivatives. Japan. Kokai 76.136.698; CA 87: 5937s (1977).
    • (1977) CA , vol.87
    • Minami, S.1    Yamabe, S.2    Sakurai, H.3    Hirose, T.4
  • 18
    • 0001376124 scopus 로고
    • On dihydropyridines. XXXV. Electrochemical oxidation of 3,5-difunctional 1,4-dihydropyridine derivatives
    • Skala V, Volke J, Ohanka V, Kuthan J (1977) On dihydropyridines. XXXV. Electrochemical oxidation of 3,5-difunctional 1,4-dihydropyridine derivatives. Collect Czech Chem Commun 42: 292-305.
    • (1977) Collect Czech Chem Commun , vol.42 , pp. 292-305
    • Skala, V.1    Volke, J.2    Ohanka, V.3    Kuthan, J.4
  • 19
    • 0020583209 scopus 로고
    • Synthesis and Antiarrhythmic and Parasympatholytic Properties of Substituted Phenols. 1. Heteroarylamine Derivatives
    • Stout DM, Matier WL, Barcelon-Yang C, Reynolds RD, Brown BS (1983) Synthesis and Antiarrhythmic and Parasympatholytic Properties of Substituted Phenols. 1. Heteroarylamine Derivatives. J Med Chem 26: 808-813.
    • (1983) J Med Chem , vol.26 , pp. 808-813
    • Stout, D.M.1    Matier, W.L.2    Barcelon-Yang, C.3    Reynolds, R.D.4    Brown, B.S.5
  • 20
    • 0017311840 scopus 로고
    • Human malaria parasites in continuous culture
    • Trager W, Jensen JB (1976) Human malaria parasites in continuous culture. Science 193: 673-675.
    • (1976) Science , vol.193 , pp. 673-675
    • Trager, W.1    Jensen, J.B.2
  • 21
    • 84986506422 scopus 로고
    • Pyrido[1′,2′:1,2]pyrimido[5,4-d]indoles. A new heterocyclic ring system
    • Unangst PC (1983) Pyrido[1′,2′:1,2]pyrimido[5,4-d]indoles. A new heterocyclic ring system. J Heterocycl Chem 20: 495-499.
    • (1983) J Heterocycl Chem , vol.20 , pp. 495-499
    • Unangst, P.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.