9-Hydroxyellipticine hydrochloride structure
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Common Name | 9-Hydroxyellipticine hydrochloride | ||
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CAS Number | 52238-35-4 | Molecular Weight | 298.76700 | |
Density | 1.349g/cm3 | Boiling Point | 557.7ºC at 760mmHg | |
Molecular Formula | C17H15ClN2O | Melting Point | N/A | |
MSDS | N/A | Flash Point | 291.1ºC |
Use of 9-Hydroxyellipticine hydrochloride9-Hydroxyellipticine hydrochloride is a inhibitor of Topo II and RyR. 9-Hydroxyellipticine hydrochloride exhibits antitumor, antioxidant and catecholamine-releasing activities. 9-Hydroxyellipticine hydrochloride exhibits IC50 values of 1.6 μM and 1.2μM in Hela S-3 and 293T cells, respectively[1][2][3]. |
Name | 5,11-dimethyl-6H-pyrido[4,3-b]carbazol-9-ol,hydrochloride |
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Synonym | More Synonyms |
Description | 9-Hydroxyellipticine hydrochloride is a inhibitor of Topo II and RyR. 9-Hydroxyellipticine hydrochloride exhibits antitumor, antioxidant and catecholamine-releasing activities. 9-Hydroxyellipticine hydrochloride exhibits IC50 values of 1.6 μM and 1.2μM in Hela S-3 and 293T cells, respectively[1][2][3]. |
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Related Catalog | |
Target |
Topoisomerase II |
In Vitro | 9-Hydroxyellipticine (9HE) causes selective inhibition of p53 protein phospborylation in Lewis lung carcinoma and SW480 (human colon cancer cell line) in a concentration-dependent manner from 0.1 to 100 μM[4]. |
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. |
References |
Density | 1.349g/cm3 |
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Boiling Point | 557.7ºC at 760mmHg |
Molecular Formula | C17H15ClN2O |
Molecular Weight | 298.76700 |
Flash Point | 291.1ºC |
Exact Mass | 298.08700 |
PSA | 48.91000 |
LogP | 4.99370 |
Ellipticine,hydrochloride |
ELLIPTICINE ANALOG |
9-HE,HCl |
9-Hydroxyellipticine HCl |
9 OHE HCl |