Desaspidin

Desaspidin
Clinical data
ATC code	P02DX01 (WHO) ;
Identifiers
	IUPAC name 2-Butanoyl-4-[(3-butanoyl-2,4-dihydroxy-6-methoxyphenyl)methyl]-3,5-dihydroxy-6,6-dimethylcyclohexa-2,4-dien-1-one;
CAS Number	114-43-2 ;
PubChem CID	8238;
ChemSpider	10295071 ;
UNII	KV3495SGKS;
KEGG	D07365 ;
ChEMBL	ChEMBL2105606 ;
CompTox Dashboard (EPA)	DTXSID6074461 ;
ECHA InfoCard	100.003.680
Chemical and physical data
Formula	C24H30O8
Molar mass	446.496 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCC(=O)C1=C(C(=C(C=C1O)OC)CC2=C(C(C(=C(C2=O)C(=O)CCC)O)(C)C)O)O;
	InChI InChI=1S/C24H30O8/c1-6-8-14(25)18-16(27)11-17(32-5)12(20(18)28)10-13-21(29)19(15(26)9-7-2)23(31)24(3,4)22(13)30/h11,27-28,30-31H,6-10H2,1-5H3 ; Key:GAHOBHHMYUYJDT-UHFFFAOYSA-N ;
	(what is this?) (verify)

Desaspidin is an anthelmintic. Desapidin may occur in natural form within some plants such as Coastal woodfern, Dryopteris arguta.[1] Since the 1950s the inhibition effects of desapidins upon phosphorylation in chloroplasts has been noted and studied.[2]

References

C. Michael Hogan. 2008. Coastal Woodfern (Dryopteris arguta}, GlobalTwitcher, ed. N. Stromberg Archived 2011-07-11 at the Wayback Machine
Bacon Kê. 2001. Photosynthesis: photobiochemistry and photobiophysics, Published by Springer, 763 pages ISBN 0-7923-6791-X, 9780792367918

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] C. Michael Hogan. 2008. Coastal Woodfern (Dryopteris arguta}, GlobalTwitcher, ed. N. Stromberg Archived 2011-07-11 at the Wayback Machine

[2] Bacon Kê. 2001. Photosynthesis: photobiochemistry and photobiophysics, Published by Springer, 763 pages ISBN 0-7923-6791-X, 9780792367918