An efficient and expeditious synthesis of a novel 5H-naphth[1',2':5,6][1,4]oxazino[2,3-b] quinoxalin-5-one and its unique inhibitory activity against a panel of human cancer cell lines

Heterocycles

Volumn 54, Issue 2, 2001, Pages 619-622

  Miyata, Fusae ^a   Yoshida, Sadamu ^b   Yamori, Takao ^c   Katoh, Tadashi ^a  

^a SAGAMI CHEMICAL RESEARCH CENTER   (Japan)

^b TOPPAN PRINTING CO LTD   (Japan)

^c CANCER INSTITUTE   (Japan)

Author keywords

Cyclization; Naphthoxazine Derivative; Quinonimine Structure; Quinoxaline Derivative; Salcomine Oxidation

Indexed keywords

5H NAPHTH[1',2':5,6][1,4]OXAZINO[2,3 B]QUINOXALIN 5 ONE; ANTINEOPLASTIC AGENT; QUINOXALINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER CELL; CANCER CHEMOTHERAPY; CANCER INHIBITION; CYCLIZATION; DRUG SYNTHESIS; HUMAN; HUMAN CELL; OXIDATION;

EID: 0035249959     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-00-s(i)101     Document Type: Article

References (13)