
Phytochemistry p. 1279 - 1288 (1982)
Update date:2022-08-04
Topics:
Beale, Michael H.
Bearder, John R.
Down, Graham H.
Hutchinson, Michael
MacMillan, Jake
Phinney, Bernard O.
The biosynthesis of 7β-hydroxy- and 7β,18-dihydroxy-kaurenolides from ent-kaur-16-en-19-oic acid has been investigated by incubating unlabelled and labelled putative intermediates with resuspension cultures of Gibberella fujikuroi.The results eliminate pathways which require the loss of oxygen from the 19-oic acid and indicate that the likely pathway is via ent-kaura-6,16-dien-19-oic acid and its ent-6α,7α-epoxide.Key Word Index - Gibberella fujikuroi; resuspension cultures; mutant B1-41a; kaurenoid biosynthesis; 7β-hydroxykaurenolide.
View MoreHangzhou Yingshanhua Pigment Chemicals Co.,Ltd.
Contact:+86-0150-58101658
Address:Nanyang Economic DevelopmentZong,Xiaoshan,Hangzhou,China
Liaoyang Xinyou Chemical Products Co.,Ltd.
Contact:+86-419-5165433 13604191870
Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Contact:86-21-58226973
Address:No 351,Guoshoujing Road, Zhangjiang Hi-tech Park, Pudong, Shanghai, China
LinHai Cina Chemical Co., LTD.
Contact:0576-85580989
Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
Zhejiang Tianyu Pharmaceutical Co., Ltd.
Contact:+86-576-84177669, 89189665,89189688,84168770
Address:Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang
Doi:10.1021/ja980474m
(1998)Doi:10.1248/cpb.37.948
(1989)Doi:10.1016/0008-6215(89)85167-5
(1989)Doi:10.1021/jo00291a023
(1990)Doi:10.1021/ja1003944
(2010)Doi:10.1039/c004636a
(2010)