Cavernosine, a novel ichthyotoxic terpenoid lactone from the sponge Fasciospongia cavernosa

DOI: 10.1002/bscb.19820910907

Source and publish data:

Bulletin des Societes Chimiques Belges p. 791 - 796 (1982)

Update date:2022-08-03

Topics: Lactone Terpenoid

Authors:

Braekman

Daloze Daloze

Bertau Bertau

Macedo de Abreu

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1002/bscb.19820910907

Cavernosine, a novel ichthyotoxic terpenoid lactone has been isolated from the sponge Fasciospongia cavernosa. Its structure has been determined by spectral analysis, chemical degradation and correlation with β-ionone.

Full text of DOI:10.1002/bscb.19820910907

Products guided by the article

Product name:(4R,5S)-5-Methyl-7-(2,6,6-trimethyl-cyclohex-1-enyl)-heptane-1,4,5-triol

Cas No:84316-06-3

R&D Labs maybe for 84316-06-3

Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China
Liaoning Yufeng Chemical Co.,Ltd.

Contact:86-0419-3418888

Address:The metallurgical industrial zone,shoushan town, Liaoyang, Liaoning, China
Chengdu Green technology Co.,Ltd.

Contact:86-28-82608355

Address:C9 ,Economic Headquarters, Economic Development Zone, Chengdu.
TIANJIN NORTH JINHENG CHEMICAL PLANT.

Contact:0086-22-59952083

Address:DongShigu Country In JiXian TianJin China
Taimai Sanluck Pharmaceutical Co.,Ltd

Contact:86-592-7662921

Address:8D,No.186,Huarong Road,Huli,Xiamen,China

Relevant to this article

Diazepines[1,4] annelated with indoline and maleimide from 3-(di)alkylamino-4-(indol-1-yl)maleimides: Mechanism of rearrangement and cyclization

Doi:10.1016/j.tet.2005.01.005
(2005)
Transition-metal Chemical Shifts in Complexes of Molybdenum(0) and Tungsten(0)

Doi:10.1039/DT9820002353
(1982)
Studies on 2-Aziridinecarboxylic Acid. VII. Formation of Dehydroamino Acid Peptides via Isomerization of Peptides Containing 2-Aziridinecarboxylic Acid by Tertiary Amines

Doi:10.1246/bcsj.55.3232
(1982)
Estrogen receptor ligands. 12. Synthesis of the major metabolites of an ERα-selective, dihydrobenzoxathiin antagonist for osteoporosis

Doi:10.1021/ol047741f
(2005)
Enamines; 42. A Simple Synthesis of 3,4-Diaminobiphenyls

Doi:10.1055/s-1982-29947
(1982)
Stereospecific Telluride-Mediated Conversion of Glycidols to Allyl Alcohols: An Extension of the Sharpless Kinetic Resolution

Doi:10.1021/jo00292a004
(1990)

Article Doi