Kusumoto, N., Ashitani, T., Murayama, T., Ogiyama, K. and Takahashi, K. (2010) Antifungal Abietane-Type Diterpenes from the Cones of Taxodium distichum Rich. Journal of Chemical Ecology, 36, 1381-1386.
http://dx.doi.org/10.1007/s10886-010-9875-2

has been cited by the following article:

• TITLE: Pharmacological Prospects of Oxygenated Abietane-Type Diterpenoids from Taxodium distichum Cones

  AUTHORS: Norihisa Kusumoto, Nobuhiro Aburai, Tatsuya Ashitani, Koetsu Takahashi, Ken-ichi Kimura

  KEYWORDS: Abietane Diterpenoid; Conifer Cone; Antibacterial Activity; 17α-Hydroxylase/C17, 20-Lyase; Prolyl Oligopeptidase; Cytotoxicity

  JOURNAL NAME: Advances in Biological Chemistry, Vol.4 No.2, March 31, 2014

  ABSTRACT: Eight naturally occurring diterpenoids, including 6,7-dehydroroyleanone, taxodal, taxodione, salvinolone, 14-deoxycoleon U, 5,6-dehydrosugiol, sandaracopimaric acid, and xanthoperol were isolated from Taxodium distichum cones and their biological properties evaluated in vitro against six different biological screening targets. Taxodione showed potent activity against a number of different targets, and salvinolone and 14-deoxycoleon U showed remarkable inhibitory activities against prolyl oligopeptidase (POP) and 17α-hydroxylase/C17,20-lyase (CYP17), respectively. These three compounds also showed strong cytotoxic activities against HL60 and K562 human leukemia cells. The structure-activity relationships of these compounds have also been considered. The findings in this study could lead to enhanced pharmacological prospects for the natural abietane-type diterpenoids consisting in conifer cones.