Structural development of benzhydrol-type 1′-Acetoxychavicol Acetate (ACA) analogs as human leukemia cell-growth inhibitors based on Quantitative Structure-Activity Relationship (QSAR) analysis

17Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

Abstract

Benzhydrol-type analogs of 1′-acetoxychavicol acetate (ACA) were developed as inhibitors of human leukemia HL-60 cell growth based on quantitative structure-activity relationship (QSAR) analysis. An analog containing an anthracenyl moiety (8) was a potent inhibitor with the IC 50 value of 0.12 μM. © 2008 Pharmaceutical Society of Japan.

Cite

CITATION STYLE

APA

Misawa, T., Aoyama, H., Furuyama, T., Dodo, K., Sagawa, M., Miyachi, H., … Hashimoto, Y. (2008). Structural development of benzhydrol-type 1′-Acetoxychavicol Acetate (ACA) analogs as human leukemia cell-growth inhibitors based on Quantitative Structure-Activity Relationship (QSAR) analysis. Chemical and Pharmaceutical Bulletin, 56(10), 1490–1495. https://doi.org/10.1248/cpb.56.1490

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free