Transformation of asterriquinone diacetate to asterriquinone monoalkyl ether via its monoacetal

Chemical and Pharmaceutical Bulletin

Volumn 44, Issue 12, 1996, Pages 2340-2341

  Kaji, Akira ^a   Saito, Ryo ^a   Shinbo, Yukako ^a   Kiriyama, Noriki ^a  

^a HOKURIKU UNIVERSITY   (Japan)

Author keywords

Aspergillus terreus IFO 6123; Asterriquinone; Asterriquinone diacetate; Asterriquinone monoacetal monoalkyl ether; Asterriquinone monoalkyl ether

Indexed keywords

ANTINEOPLASTIC AGENT; ASTERRIQUINONE DIACETATE; DRUG METABOLITE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTINEOPLASTIC ACTIVITY; ARTICLE; ASPERGILLUS TERREUS; CANCER INHIBITION; CHEMICAL REACTION; DRUG POTENCY; DRUG SYNTHESIS; DRUG TRANSFORMATION; GROWTH INHIBITION; LEUKEMIA CELL; LEUKEMIA P 388; MOUSE; NONHUMAN;

EID: 0030477070     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.44.2340     Document Type: Article

References (6)

1. a) Yamamoto Y., Nishimura K., Kiriyama N., Chem. Pharm. Bull., 24, 1853-1859 (1976);
2. b) Kaji A., Iwata T., Kiriyama N., Wakusawa S., Miyamoto K., Chem. Pharm. Bull., 42, 1682-1684 (1994).
3. Kaji A., Kimura K., Iwata T., Kiriyama N., Chem. Pharm. Bull., 43, 1818-1820 (1995).
4. 2), 6.36 (1H, s, OH), 7.12-7.19 (4H, m, Ar-H), 7.49-7.51 (1H, m, Ar-H), 7.57-7.60 (2H, m, Ar-H), 7.66 (1H, s, Ar-H), 7.83-7.85 (1H, m, Ar-H), 7.93 (1H, s, Ar-H).
5. Swenton J. S., "The Chemistry of the Quinonoid Compounds," Vol. 2, Part 2, ed. by Patai S. and Rappoport Z., John Wiley and Sons, Inc., New York, 1988, p. 899.
6. 2.