Nomenclature
CAS number: 477-27-0
N-[(7
S)-5,6,7,9-Tetrahydro-10-hydroxy-1,2,3-trimethoxy-9-oxobenzo[
a]heptalen-7-yl]acetamide; 7-acetamido-10-hydroxy-1,2,3-trimethoxy-6,7-dihydrobenzo[
a]heptalen-9(5
H)-one.
C
21H
23NO
6; mol wt 385.41.
C 65.44%, H 6.02%, N 3.63%, O 24.91%.
Description and references
Deriv of colchicine, q.v., isolated from Colchicum autumnale L., Liliaceae: Santavy, Macák, Collect.
Czech. Chem. Commun. 19, 805 (1954). Toxicity
data: B. Goldberg et al., Cancer 3, 124 (1950). Structure and synthesis: Nakamura, Chem. Pharm. Bull. 10, 299 (1962).
Circular dichroism: J. Hrbek et al., Collect. Czech. Chem. Commun. 47, 2258 (1982).
Effect on antibody response induced in vitro: J. Sterzl et al., Folia Microbiol. 27, 256 (1982).
Properties
Yellow crystals from dioxane + ether, mp 178-179°. [α]D25 -255.1° (c = 1 in chloroform). uv max (95%
ethanol): 351, 244 nm (log ε 4.28, 4.51). Slightly
sol in water; freely sol in alcohol, chloroform. Almost insol in benzene,
ether.Derivative
Ethyl ether.
C
23H
27NO
6; mol wt 413.46.
C 66.81%, H 6.58%, N 3.39%, O 23.22%.
Properties
Needles from ethyl acetate + ether, mp 135-139°. [α]D25 -129.4° (c = 1
in chloroform). uv max (95% ethanol):
351, 243.5 nm (log ε 4.21, 4.45). LD50 i.p. in mice:
84 mg/kg (Goldberg).