Title: Ellipticine
CAS Registry Number: 519-23-3
CAS Name: 5,11-Dimethyl-6
H-pyrido[4,3-
b]carbazole
Molecular Formula: C17H14N2
Molecular Weight: 246.31
Percent Composition: C 82.90%, H 5.73%, N 11.37%
Literature References: Antitumor alkaloid isolated from
Ochrosia elliptica Labill.,
O. sandwicensis A. DC.,
O. viellardii, O. silvatica, Apocynaceae: Goodwin
et al., J. Am. Chem. Soc. 81, 1903 (1959); Kan Fan
et al., Phytochemistry 9, 1351 (1970); Cosson, Schmid,
ibid. 1353. Structure and synthesis: Woodward
et al., J. Am. Chem. Soc. 81, 4434 (1959). Syntheses: J. Bergman, R. Carlsson,
Tetrahedron Lett. 1977, 4663; D. A. Taylor
et al., J. Chem. Res. Miniprint 1979, 4801; S. Kano
et al., J. Org. Chem. 46, 2979 (1981); R. Besselievre, H. P. Husson,
Tetrahedron 37, 241 (1981). Regioselective synthesis: T.-L. Ho, S.-Y. Hsieh,
Helv. Chim. Acta 89, 111 (2006). Toxicity study: Rakieten
et al., U.S. Gov. Res. Dev. Rep. 67, 38 (1967),
C.A. 68, 20827g (1968). Review of syntheses: M. Sainsbury,
Synthesis 1977, 437-448; R. Barone, M. Chanon,
Heterocycles 16, 1357-1365 (1981). Review of antineoplastic activity: K. W. Kohn
et al., Antibiotics vol. 5 (pt. 2), F. E. Hahn, Ed. (Springer-Verlag, New York, 1979) pp 195-213.
Properties: Bright yellow needles from ethyl acetate, mp 311-315° (dec). uv max: 239, 277, 286, 294, 332, 382, 400 nm (log e 4.23, 4.61, 4.76, 4.74, 3.65, 3.61, 3.53). LD50 in mice (mg/kg): 19.5-22.4 i.v.; 178-204 orally (Rakieten).
Melting point: mp 311-315° (dec)
Absorption maximum: uv max: 239, 277, 286, 294, 332, 382, 400 nm (log e 4.23, 4.61, 4.76, 4.74, 3.65, 3.61, 3.53)
Toxicity data: LD50 in mice (mg/kg): 19.5-22.4 i.v.; 178-204 orally (Rakieten)