Digitoxigenin

Digitoxigenin^[1]
Names
	IUPAC name 3β,14-Dihydroxy-5β-card-20(22)-enolide
	Systematic IUPAC name 4-[(1R,3aS,3bR,5aR,7S,9aS,9bS,11aR)-5a,7-Dihydroxy-9a,11a-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]furan-2(5H)-one
	Other names 3-β,14-dihydroxy-5-β,14-β-card-20(22)-enolide; 5β-Card-20(22)-enolide, 3β,14-dihydroxy-; Card-20(22)-enolide, 3,14-dihydroxy-, (3β,5β)-; NSC 407806; Δ20:22-3,14,21-Trihydroxynorcholenic acid lactone; cerberigenin; echujetin; evonogenin; thevetigenin
Identifiers
CAS Number	143-62-4 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	95448
ChEMBL	ChEMBL1453;
ChemSpider	3571902;
ECHA InfoCard	100.005.095
EC Number	205-603-4;
PubChem CID	4369270;
RTECS number	FH4975000;
UNII	S63WOD4VOL ;
CompTox Dashboard (EPA)	DTXSID80162276 ;
	InChI InChI=1S/C23H34O4/c1-21-8-5-16(24)12-15(21)3-4-19-18(21)6-9-22(2)17(7-10-23(19,22)26)14-11-20(25)27-13-14/h11,15-19,24,26H,3-10,12-13H2,1-2H3/t15-,16+,17-,18+,19-,21+,22-,23+/m1/s1 Key: XZTUSOXSLKTKJQ-CESUGQOBSA-N; InChI=1/C23H34O4/c1-21-8-5-16(24)12-15(21)3-4-19-18(21)6-9-22(2)17(7-10-23(19,22)26)14-11-20(25)27-13-14/h11,15-19,24,26H,3-10,12-13H2,1-2H3/t15-,16+,17-,18+,19-,21+,22-,23+/m1/s1 Key: XZTUSOXSLKTKJQ-CESUGQOBBG;
	SMILES O=C/1OCC(=C\1)\[C@@H]2[C@@]4([C@](O)(CC2)[C@@H]5CC[C@@H]3C[C@@H](O)CC[C@]3(C)[C@H]5CC4)C;
Properties
Chemical formula	C23H34O4
Molar mass	374.51
Appearance	solid
Melting point	252 to 253 °C (486 to 487 °F; 525 to 526 K)
Hazards
	Occupational safety and health (OHS/OSH):
Main hazards	Toxic
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Digitoxigenin, a cardenolide, is the aglycone of digitoxin.

Digitoxigenin can be used to prepare actodigin.^[2]

In Lednicer's book on steroids, it is made from deoxycholic acid.

References

↑ http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=D9404%7CSIGMA&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC
↑ Ferland, J. M. (1974). "Synthetic Cardenolides and Related Products. III. Isocardenolides". Canadian Journal of Chemistry. 52 (9): 1652–1661. doi:10.1139/v74-239. ISSN 0008-4042.

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

[1] ttp://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=D9404%7CSIGMA&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC

[Ferland1974-2] Ferland, J. M. (1974). "Synthetic Cardenolides and Related Products. III. Isocardenolides". Canadian Journal of Chemistry. 52 (9): 1652–1661. doi:10.1139/v74-239. ISSN 0008-4042.

[1]

[2]