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Postion:Product Catalog >Pixantrone hydrochloride
Pixantrone hydrochloride
  • Pixantrone hydrochloride

Pixantrone hydrochloride NEW

Price $2140 $2785 $3520
Package 25mg 50mg 100mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-05-01

Product Details

Product Name: Pixantrone hydrochloride CAS No.: 175989-38-5
Supply Ability: 10g Release date: 2025/05/01

Product Introduction

Bioactivity

NamePixantrone hydrochloride
DescriptionPixantrone (BBR 2778 (free base)) hydrochloride, a mitoxantrone analog, functions as a topoisomerase II inhibitor and DNA intercalator, demonstrating anti-tumor activity [1] [2].
In vitroPixantrone hydrochloride demonstrates a broad spectrum of anticancer activities, affecting various cancer cell lines through multiple mechanisms. At concentrations ranging from 0 to 10 μM over 72 hours, it induces cell death across different cancer cell lines without disrupting the cell cycle. Additionally, when applied at concentrations between 25 to 500 nM for 24 hours, pixantrone hydrochloride leads to DNA damage, impedes chromosome segregation, and results in significant chromosomal aberrations and mitotic catastrophes in PANC1 cells. Its ability to inhibit the growth of human leukemia K562 cells, etoposide-resistant K/VP.5 cells, MDCK, and ABCB1-transfected MDCK/MDR cells is evidenced by IC50s of 0.10 μM, 0.56 μM, 0.058 μM, and 4.5 μM, respectively, achieved at concentrations between 0 and 100 μM over 72 hours. Additionally, at dosages from 0.01 to 0.2 μM, it facilitates a concentration-dependent formation of linear DNA by targeting topoisomerase IIα and generating semiquinone free radicals in an enzymatic reducing system, a process not observed in cellular systems likely due to minimal cellular uptake. At concentrations from 0.01 to 10 μM, pixantrone hydrochloride significantly inhibits the proliferation of rat 97-116 peptide-specific T cells, indicating potent immunosuppressive activity. In cell proliferation assays, it was shown to decrease the proliferation of T47D, MCF-10A, and OVCAR5 cells at 37.3 nM, 126 nM, and 136 nM, respectively, and effectively suppressed rat T cell proliferation at a concentration of 0.01 μM, achieving complete suppression at higher concentrations.
In vivoPixantrone hydrochloride (i.v., 27 mg/kg, every 7 days, for three treatments) does not exacerbate existing moderate degenerative cardiomyopathy and exhibits minimal cardiotoxicity in mice, even after multiple treatment cycles, leading to lower mortality rates compared to mitoxantrone in doxorubicin-pretreated mice [3]. Additionally, Pixantrone hydrochloride (i.v., 16.25 mg/kg, weekly, for three treatments) effectively modulates Lymph node cells (LNC) responses, influences T cell subpopulations in TAChR-immunized Lewis rats, and demonstrates both preventive and therapeutic effects in experimental autoimmune myasthenia gravis (EAMG) rats [4].
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

Company Profile Introduction

TargetMol Chemicals Inc. is headquartered in Boston, MA, and specializes in products and services that serve the research needs of chemical and biological scientists worldwide. With a client base in 40+ countries, TargetMol has evolved into one of the biggest global research suppliers for compound libraries and small molecule compounds. 170+ Compound Libraries, 10000+ Noval Small Molecucles,16000+ Nature Compounds TargetMol diligently updates and offers over 170 types of compound libraries and a wide range of high-quality research chemicals, including inhibitors, activators, natural products, peptides, antibodies , and novel life-science kits for laboratory and scientific use. In addition, our lab allows us to conduct CADD (computer-aided drug design) and chemical synthesis to meet the customization needs of our clients.

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