Pixantrone hydrochloride
Based on 3 publication(s) in Google Scholar
Pixantrone (BBR 2778 (free base)) hydrochloride, a mitoxantrone analog, is a topoisomerase II inhibitor and DNA intercalator, with anti-tumor activity.
Para uso exclusivo en investigación. No vendemos a pacientes.
- No. CAS: 175989-38-5
- Fòrmula: C17H20ClN5O2
- Peso molecular:361.83
-
Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Actividad biológica
-
Chemical Information
- Pureza y Documentación
- Referencias
-
Help & FAQs
Publications Citing Use of MedChemExpress (MCE) Pixantrone hydrochloride
MoreVer todos los productos específicos de isoformas Topoisomerase
More
Actividad biológica
Descripciòn
IC50 & Target
[1]|
Topoisomerase II |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| L1210 | IC50 |
0.01 μg/mL
Compound: 3c
|
Tested in vitro for inhibitory activity against L1210 murine leukemia
Tested in vitro for inhibitory activity against L1210 murine leukemia
|
[PMID: 8145234] |
In Vitro
Pixantrone (0-10 μM, 72 h) hydrochloride induces cell death in multiple cancer cell lines independent of cell cycle perturbation[1].
Pixantrone (25-500 nM, 24 h) hydrochloride can induce DNA damage, hinder chromosome segregation, and induce severe chromosomal aberrations and mitotic catastrophes in PANC1 cells[1].
Pixantrone (0-100 μM, 72 h) hydrochloride potently inhibits growth of human leukemia K562 cells, etoposide-resistant K/VP.5 cells, MDCK and ABCB1-transfected MDCK/MDR cells with IC50s of 0.10 μM, 0.56 μM, 0.058 μM and 4.5 μM, respectively[2].
Pixantrone (0.01-0.2 μM) hydrochloride leads to a concentration-dependent formation of linear DNA through acting on topoisomerase IIα and produces semiquinone free radicals in an enzymatic reducing system, although not in a cellular system, most likely due to low cellular uptake[2].
Pixantrone (0.01-10 μM) hydrochloride shows potent inhibitory activities against rat 97-116 peptide-specific T cell proliferation[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:T47D, MCF-10A and OVCAR5 cells
-
Concentration:0-10 μM
-
Incubation Time:72 h
-
Result:Reduced the proliferation of T47D, MCF-10A and OVCAR5 cells with 37.3 nM, 126 nM and 136 nM, respectively.
-
Cell Line:Lewis rat T cell lines
-
Concentration:0.01-10 μM
-
Incubation Time:
-
Result:Inhibited 39.3% rat 97-116 peptide-specific T cells proliferation at 0.01 μM and completely suppressed T cell proliferation at high concentrations.
In Vivo
Pixantrone (i.v., 16.25 mg/kg, every week, three times) hydrochloride modulates Lymph node cells (LNC) responses, affacts T cell subpopulations in TAChR-immunized Lewis rats and also shows preventive and therapeutic effect in experimental autoimmune myasthenia gravis (EAMG) rats[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
No. CAS 175989-38-5
-
Peso molecular 361.83
-
Fòrmula C17H20ClN5O2
-
SMILES
O=C(C1=C(NCCN)C=CC(NCCN)=C12)C3=C(C=NC=C3)C2=O.Cl
-
Synonyms
BBR 2778 hydrochloride
-
Envío
Room temperature in continental US; may vary elsewhere.
-
Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (3)
-
Journal Impact Factor
-
Most Recent
-
Sci Data
High-throughput drug screening identifies novel therapeutics for Low Grade Serous Ovarian Carcinoma. [Abstract]2024 Sep 19;11(1):1024. PMID: 39300112 -
J Mol Med (Berl)
2019 Aug;97(8):1183-1193. PMID: 31201471 -
Methods Mol Biol
2018:1711:351-398. PMID: 29344898
Pureza y Documentación
Referencias
[1]. Neil Beeharry, et al. Pixantrone induces cell death through mitotic perturbations and subsequent aberrant cell divisions. Cancer Biol Ther. 2015;16(9):1397-406. [Content Brief]
[2]. Brian B Hasinoff, et al. Mechanisms of Action and Reduced Cardiotoxicity of Pixantrone; a Topoisomerase II Targeting Agent with Cellular Selectivity for the Topoisomerase IIα Isoform. J Pharmacol Exp Ther. 2016 Feb;356(2):397-409. [Content Brief]
[3]. Ennio Cavalletti, et al. Pixantrone (BBR 2778) has reduced cardiotoxic potential in mice pretreated with doxorubicin: comparative studies against doxorubicin and mitoxantrone. Invest New Drugs. 2007 Jun;25(3):187-95. [Content Brief]
[4]. Federica Ubiali, et al. Pixantrone (BBR2778) reduces the severity of experimental autoimmune myasthenia gravis in Lewis rats. J Immunol. 2008 Feb 15;180(4):2696-703. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Pixantrone hydrochloride Related Classifications
HY-13727B Related Classifications
Powered by Bioz