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Volumn 43, Issue 1, 1998, Pages 39-41

Antifungal Effects of New Heterocyclic Compounds, 6H-Pyrimido[2,1-a]isoindole Derivatives

Author keywords

[No Author keywords available]

Indexed keywords

BACILLUS SUBTILIS; ESCHERICHIA COLI; SACCHAROMYCES CEREVISIAE;

EID: 0031638711     PISSN: 00155632     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02815539     Document Type: Article
Times cited : (15)

References (11)
  • 1
    • 25744461266 scopus 로고
    • Heterocyclic Antibiotics, CRC Press, Boca Raton
    • BÉRDY J.: CRC Handbook of Antibiotic Compounds, Vol. V, Heterocyclic Antibiotics, p. 133. CRC Press, Boca Raton 1981.
    • (1981) CRC Handbook of Antibiotic Compounds , vol.5 , pp. 133
    • Bérdy, J.1
  • 2
    • 0023151996 scopus 로고
    • Synthesis, biological evaluation, and quantitative structure-activity relationship analysis of 2-hydroxy-1H-isoindolediones as new cytostatic agents
    • CHAN C.L., LIEN E.J., TOKES Z.A.: Synthesis, biological evaluation, and quantitative structure-activity relationship analysis of 2-hydroxy-1H-isoindolediones as new cytostatic agents. J.Med.Chem. 30, 509-514 (1987).
    • (1987) J. Med. Chem. , vol.30 , pp. 509-514
    • Chan, C.L.1    Lien, E.J.2    Tokes, Z.A.3
  • 3
    • 0014868877 scopus 로고
    • The absolute configuration of indolmycin
    • CHAN T.H., HILL R.K.: The absolute configuration of indolmycin. J.Org.Chem. 35, 3519-3520 (1970).
    • (1970) J. Org. Chem. , vol.35 , pp. 3519-3520
    • Chan, T.H.1    Hill, R.K.2
  • 4
    • 84988164738 scopus 로고
    • Formation of new antimicrobial 13H-1,5-benzenodiazepino[2,3-b]quinoxaline during the reaction of 4-deoxy-2,3-aldosdiuloses with o-phenylenediamine
    • GABRIEL J., POSPÍŠEK M., PALKOVÁ Z., NĚMEČEK J., HAVLÍČEK V., VOLC J., KUBÁTOVÁ E.: Formation of new antimicrobial 13H-1,5-benzenodiazepino[2,3-b]quinoxaline during the reaction of 4-deoxy-2,3-aldosdiuloses with o-phenylenediamine. Pharm.Sci. 1, 581-583 (1995).
    • (1995) Pharm. Sci. , vol.1 , pp. 581-583
    • Gabriel, J.1    Pospíšek, M.2    Palková, Z.3    Němeček, J.4    Havlíček, V.5    Volc, J.6    Kubátová, E.7
  • 5
    • 0348188404 scopus 로고
    • Criteria of the differences of the products of condensation of α-aminoazaheterocycles with β-keto esters as an example of the isomeric pyrimidoisoindoles
    • ISCHENKO V.V., KOVTUNENKO V.A., TYLTIN A.K., TRACHEVSKI V.V., VŠETEČKA V., BABICHEV F.S.: Criteria of the differences of the products of condensation of α-aminoazaheterocycles with β-keto esters as an example of the isomeric pyrimidoisoindoles. (In Russian) Ukr.Khim.Zh. 56, 517-521 (1990).
    • (1990) Ukr. Khim. Zh. , vol.56 , pp. 517-521
    • Ischenko, V.V.1    Kovtunenko, V.A.2    Tyltin, A.K.3    Trachevski, V.V.4    Všetečka, V.5    Babichev, F.S.6
  • 6
    • 0001398756 scopus 로고
    • The structure and synthesis of pimprinine
    • JOSHI B.S., TAYLOR W.I.: The structure and synthesis of pimprinine. Tetrahedron 19, 1437-1439 (1963).
    • (1963) Tetrahedron , vol.19 , pp. 1437-1439
    • Joshi, B.S.1    Taylor, W.I.2
  • 7
    • 0023197560 scopus 로고
    • Nitration of 3-acylindoles in the presence of metal MeCN solvates and synthesis of the antibiotic alkaloid chuangxinmycin
    • MURASE M., KOIKE T., MORIYA Y., TOBINAGA S.: Nitration of 3-acylindoles in the presence of metal MeCN solvates and synthesis of the antibiotic alkaloid chuangxinmycin. Chem.Pharm.Bull. 35, 2656-2660 (1987).
    • (1987) Chem. Pharm. Bull. , vol.35 , pp. 2656-2660
    • Murase, M.1    Koike, T.2    Moriya, Y.3    Tobinaga, S.4
  • 8
    • 0025683292 scopus 로고
    • Cyclopiazonic acid: Toxicity and tissue distribution
    • NORRED W.P.: Cyclopiazonic acid: toxicity and tissue distribution. Vet.Hum.Toxicol. 32 (Suppl.), 20-25 (1990).
    • (1990) Vet. Hum. Toxicol. , vol.32 , Issue.SUPPL. , pp. 20-25
    • Norred, W.P.1
  • 9
    • 0016217689 scopus 로고
    • Antimicrobial activities of indole
    • OIMOMI M.: Antimicrobial activities of indole. J.Antibiot. 27, 987-988 (1974).
    • (1974) J. Antibiot. , vol.27 , pp. 987-988
    • Oimomi, M.1
  • 10
    • 0022542995 scopus 로고
    • Thromboxane synthetase inhibitors and antihypertensive agents. 2. N-[(1H-imidazol-1-yl)alkyl]-1H-isoindole-1,3(2H)-diones and N-[(1H-1,2,4-triazol-1-yl)alkyl]-1H-isoindole-1,3(2H)-diones as unique antihypertensive agents
    • PRESS J.B., WRIGHT W.B. Jr., CHAN P.S., MARSICO J.W., HAUG M.F., TAUBER J., TOMCUFCIK A.S.: Thromboxane synthetase inhibitors and antihypertensive agents. 2. N-[(1H-imidazol-1-yl)alkyl]-1H-isoindole-1,3(2H)-diones and N-[(1H-1,2,4-triazol-1-yl)alkyl]-1H-isoindole-1,3(2H)-diones as unique antihypertensive agents. J.Med.Chem. 29, 816-819 (1986).
    • (1986) J. Med. Chem. , vol.29 , pp. 816-819
    • Press, J.B.1    Wright W.B., Jr.2    Chan, P.S.3    Marsico, J.W.4    Haug, M.F.5    Tauber, J.6    Tomcufcik, A.S.7
  • 11
    • 0023513850 scopus 로고
    • Pharmacological properties of SM-3997: A new anxioselective anxiolytic candidate
    • SHIMIZU H., HIROSE A., TATSUNO T., NAKAMURA M., KATSUBE J.: Pharmacological properties of SM-3997: a new anxioselective anxiolytic candidate. Japan J.Pharmacol. 45, 493-500 (1987).
    • (1987) Japan J. Pharmacol. , vol.45 , pp. 493-500
    • Shimizu, H.1    Hirose, A.2    Tatsuno, T.3    Nakamura, M.4    Katsube, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.