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Volumn 336, Issue 6-7, 2003, Pages 336-344

Novel high energy intermediate analogues with a triazasterol structure as potential ergosterol biosynthesis inhibitors IV: Antimicrobial activity of mono-, bi-, and tricyclic 8,13,15-triazasteroid analogues including the synthesis of novel 4-alkylamino- and 4-alkenylamino-9-hydroxypyrimidoisoquinolines

Author keywords

2 Imidazolin 2 amines, N2 and N 2 4 substituted; 4 Alkylamino and 4 alkenylamino 9 hydroxy; Guanidines, N Alkyl N (phenethyl and cyclohexenylethyl); Tetrahydro 2H pyrimido 4,3 a isoquinolines

Indexed keywords

4 (6 ISOPROPYL 3 METHYL 6 HEPTENYLAMINO) 9 HYDROXYPYRIMIDOISOQUINOLINE; 4 AMINO 9 HYDROXY 1,6,7,11B TETRAHYDRO 2H PYRIMIDO[4,3 A]ISOQUINOLINE; 9 HYDROXYPYRIMIDOISOQUINOLINE; 9 METHOXYPYRIMIDOISOQUINOLINE; 9 METHOXYTHIONE; AMINOHYDROXYPYRIMIDOISOQUINOLINE; BICYCLIC 8,13,15 TRIAZASTEROID DERIVATIVE; ERGOSTEROL; MONOCYCLIC 8,13,15 TRIAZASTEROID DERIVATIVE; N' (CYCLOHEXENYLETHYL)GUANIDINE; N' (PHENETHYL)GUANIDINE; N4 AMINOPYRIMIDOISOQUINOLINE; TRIAZASTEROL DERIVATIVE; TRICYCLIC 8,13,15 TRIAZASTEROID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0041321080     PISSN: 03656233     EISSN: None     Source Type: Journal    
DOI: 10.1002/ardp.200300774     Document Type: Article
Times cited : (9)

References (22)
  • 3
    • 0026567044 scopus 로고
    • N. S. Ryder, Br. J. Dermatol. 1992, 126 (Suppl. 39), 2-7.
    • (1992) Br. J. Dermatol. , vol.126 , Issue.SUPPL. 39 , pp. 2-7
    • Ryder, N.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.