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Postion:Product Catalog >Palbociclib orotate
Palbociclib orotate
  • Palbociclib orotate

Palbociclib orotate NEW

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Package 5mg 50mg
Supply Ability: 10g
Update Time: 2026-05-11

Product Details

Product Name: Palbociclib orotate CAS No.: 2757498-64-7
Supply Ability: 10g Release date: 2026/05/11

Product Introduction

Bioactivity

NamePalbociclib orotate
DescriptionPalbociclib (PD 0332991) orotate, an orally active selective inhibitor of CDK4 and CDK6, exhibits IC50 values of 11 and 16 nM, respectively. This compound demonstrates potent anti-proliferative effects and induces cell cycle arrest in cancer cells, applicable in research concerning HR-positive, HER2-negative breast cancer, and hepatocellular carcinoma [1] [3] [4].
In vitroPalbociclib orotate, at concentrations ranging from 0–1 μM over 24 hours, effectively inhibits Ser 795 phosphorylation in MDA-MB-435 cells, demonstrating an IC50 of 0.063 μM, and similarly impacts Ser 780 and Ser 795 phosphorylation in Colo-205 colon carcinoma cells [1]. At a wider concentration range of 0–10 μM for the same duration, it induces a G1 phase cell cycle arrest in MDA-MB-453 cells [1]. When administered at 500 nM for seven days, palbociclib orotate upregulates homologous gene expression (H2d1, H2k1, and B2m) in both MDA-MB-453 and MDA-MB-361 cells [2]. Additionally, with extended exposure of six days, palbociclib orotate suppresses the growth of various luminal ER-positive and HER2-amplified breast cancer cell lines, with IC50 values spanning from 4 nM to 1 μM [3]. Over a three-day period, it also limits the proliferation of human liver cancer cell lines with IC50 values between 0.01 μM and 3.49 μM and causes reversible cell cycle arrest [4].
In vivoPalbociclib orotate, administered orally at doses of 75 or 150 mg/kg daily for 14 days, induces rapid tumor regression and impedes tumor growth [1]. At a dose of 90 mg/kg for 12 days, it also decreases Treg cell quantities and alters the Treg:CD8 ratio in the spleen and lymph nodes of tumor-free mice, highlighting its tumor-independent actions [2]. Furthermore, when given at 100 mg/kg for a week, palbociclib orotate exhibits potent anti-tumor effects in a genetically engineered mosaic mouse model of liver cancer [4].
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Inhibitors RelatedRibociclib | (E)-β-Farnesene | Amantadine | 2-Chloropyrazine | Kojic acid | Abemaciclib | 2,4,6-Trihydroxybenzoic acid | Palbociclib | Abemaciclib methanesulfonate | Sodium Oxamate | Seliciclib | Dinaciclib

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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TargetMol Chemicals Inc.

2YR United StatesUnited States
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, Massachusetts, USA
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