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52238-35-4

52238-35-4 Structure

52238-35-4 Structure
IdentificationBack Directory
[Name]

Nsc264136
[CAS]

52238-35-4
[Synonyms]

Nsc264136
9-hydroxyellipticine HCl salt
9-Hydroxyellipticine, Hydrochloride
[Molecular Formula]

C17H15ClN2O
[MDL Number]

MFCD02683589
[MOL File]

52238-35-4.mol
[Molecular Weight]

298.767
Chemical PropertiesBack Directory
[Melting point ]

>223oC (dec.)
[storage temp. ]

Hygroscopic, -20°C Freezer, Under inert atmosphere
[solubility ]

DMSO (Slightly, Heated), Methanol (Slightly, Sonicated)
[form ]

Solid
[color ]

Orange to Dark Orange
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Description]

9-Hydroxyellipticine is a derivative of ellipticine with diverse biological activities. It inhibits aroclor-induced activation of aniline hydroxylase, aminopyrine N-demethylase, and 7-ethoxycourmarin O-deethylase in rat liver microsomes (Kis = 3.5, 0.6, and 0.74 μM, respectively). 9-Hydroxyellipticine inhibits the growth of L1210 murine leukemia cells (IC50 = 3 nM) in vitro and increases survival in an L1210 mouse leukemia model. It inhibits carrageenan-induced edema and UV-induced erythema in guinea pigs.
[Uses]

9-Hydroxyellipticine Hydrochloride is a potent topoisomerase II inhibitor.
[in vivo]

9-Hydroxyellipticine (5 or 10 mg/kg, ip) results in chromosome clumping and sister chromatid exchange in murine bone marrow cells[1].

Animal Model:Three- to five-month-old C57B1/6 male mice[1].
Dosage:5 or 10 mg/kg.
Administration:IP.
Result:Resulted in chromosome clumping, chromatid aberrations, and micronuclei formation in murine bone marrow cells.
[IC 50]

Topoisomerase II
[References]

[1] PIERRE LESCA . A class of strong inhibitors of microsomal monooxygenases: The elupticines[J]. Chemico-Biological Interactions, 1979, 24 2: Pages 189-197. DOI: 10.1016/0009-2797(79)90007-3
[2] M MONNOT. DNA-drug recognition and effects on topoisomerase II-mediated cytotoxicity. A three-mode binding model for ellipticine derivatives.[J]. The Journal of Biological Chemistry, 1991, 266 3: 1820-1829.
[3] J B LE PECQ. Antitumor activity of 9-hydroxyellipticine (NSC 210717) ON L1210 mouse leukemia and the effect of route of injection.[J]. Cancer research, 1976, 36 9 pt.1: 3067-3076.
[4] J CROS  N D X  A Thibault. [Anti-inflammatory effect of hydroxy-9-ellipticine].[J]. Comptes rendus hebdomadaires des seances de l’Academie des sciences. Serie D: Sciences naturelles, 1975, 281 15: 1139-1142.
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