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Volumn 60, Issue 6, 2003, Pages 1359-1366

Synthesis and COX-2 inhibitory activities of rutaecarpine homologues

Author keywords

[No Author keywords available]

Indexed keywords

2,3 POLYMETHYLENE 4(3H) QUINAZOLINONE; 7,12 DIHYDROINDOLO[2',3':3,4]PYRROLO[2,1 B]QUINAZOLIN 5 ONE; 7,8,9,14 TETRAHYDRO 5H INDOLO[2',3':3,4]AZEPINO[2,1 B]QUINAZOLIN 5 ONE; CARBENE; CYCLOOXYGENASE 1; CYCLOOXYGENASE 2; CYCLOOXYGENASE 2 INHIBITOR; INDOLE DERIVATIVE; INDOMETACIN; N (2 CYCLOHEXYLOXY 4 NITROPHENYL)METHANESULFONAMIDE; QUINAZOLINONE DERIVATIVE; RUTAECARPINE; RUTAECARPINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0038485774     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-03-9744     Document Type: Article
Times cited : (23)

References (23)
  • 3
    • 0003118854 scopus 로고
    • J. H. Chu, Science Record (China) 1951, 4, 479 (Chem. Abstr., 1952, 46, 11589b).
    • (1952) Chem. Abstr. , vol.46
  • 17
    • 0037572972 scopus 로고    scopus 로고
    • note
    • Assignments of 2aa and 2ab are based on the following NOE spectral data: equation presented
  • 20
    • 0000425265 scopus 로고
    • The mp's of 3,3′-mono-, di-, and trimethylene-2,2′-bipyridines are 172 °C, 152-153 °C, and 141 °C, respectively: R. P. Thummel, F. Lefoulon, and R. Mahadevan, J. Org. Chem., 1985, 50, 3824.
    • (1985) J. Org. Chem. , vol.50 , pp. 3824
    • Thummel, R.P.1    Lefoulon, F.2    Mahadevan, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.