Nomenclature
CAS number: 630-60-4
(1β,3β,5β,11α)-3-[(6-Deoxy-α-
l-mannopyranosyl)oxy]-1,5,11,14,19-pentahydroxycard-20(22)-enolide; G-strophanthin; Gratus strophanthin; acocantherin.
C
29H
44O
12; mol wt 584.65.
C 59.58%, H 7.59%, O 32.84%.
Description and references
Obtained from the seeds of Strophanthus
gratus (Wall. & Hock.) Baill.; also occurs in Acokanthera
ouabaio Cathel and other A. spp, Apocynaceae. Isoln: Schwartze et al., J.
Pharmacol. 36, 481 (1929). Hydrolysis yields
one mol ouabagenin and one mol rhamnose: Jacobs, Bigelow, J. Biol. Chem. 96, 647 (1932).
Toxicity study: Small et al., Toxicol. Appl. Pharmacol. 20, 44 (1971). See also Fieser, Fieser, Steroids (1959, Reinhold, New York; Chapman & Hall, London) pp 768, 772;
Reichstein, Reich, Annu. Rev. Biochem. 15, 155 (1946).
Derivative
Octahydrate.
Nomenclature
Purostrophan (Kali-Chemie); Strodival (Herbert); Strophoperm (Sertürner). Properties
Shiny plates (from water) which give up their
water of crystn at 130°. When anhydr dec about 190°. [α]D25 -31 to -32.5° (c = 1 calcd as anhydr). Stable in air, but affected by light.
One gram dissolves in about 75 ml water, in 5 ml boiling water, in
100 ml alcohol, in 8 ml boiling alcohol. Also sol in amyl alcohol,
dioxane. Slightly sol in ether, chloroform, ethyl acetate. Aq solns
are neutral to litmus. LD50 i.v. in rats: 14 mg/kg (Small).Cardiotonic.
Cardiotonic, diuretic.