Products Categories

    Selleck China

    Country: Country China (Mainland)

    Business Type: Trading Company

    qq

  • Ms.Olivia
    Tel: 400-668-6834

  • Mobile:
  • Tel:400-668-6834
  • Fax:
  • Province/state:Shanghai
  • City:Shanghai
  • Street:Building 3, No. 88 Chenhui Road, Kingdee Software Park, Pudong New District, Shanghai, China
  • MaxCard:
Home > Products >  Palbociclib (PD-0332991) HCl

Palbociclib (PD-0332991) HCl CAS NO.827022-32-2

  • Min.Order: 5 Metric Ton
  • Payment Terms:
  • Product Details

Keywords

  • Palbociclib HCl
  • PD-0332991 HCl
  • CDK inhibitor

Quick Details

  • ProName: Palbociclib (PD-0332991) HCl
  • CasNo: 827022-32-2
  • Molecular Formula: C24H29N7O2.HCl
  • ProductionCapacity: Metric Ton/Day
  • Purity: >97%
  • LimitNum: 5 Metric Ton

Superiority

Biological Activity

 

Description Palbociclib (PD-0332991) HCl is a highly selective inhibitor of CDK4/6 with IC50 of 11 nM/16 nM in cell-free assays, respectively. It shows no activity against CDK1/2/5, EGFR, FGFR, PDGFR, InsR, etc. Phase 3.
Features Non-cytotoxic, and halts cancer cell growth & could be used in glioblastoma that has relapsed after temozolomide treatment (a chemotherapeutic used to treat many cancers).
Targets
CDK4/CyclinD3 [1]
(Cell-free assay)
CDK4/CyclinD1 [1]
(Cell-free assay)
CDK6/CyclinD2 [1]
(Cell-free assay)
9 nM 11 nM 15 nM
In vitro

PD 0332991 has little effect on other protein kinases including EGFR, FGFR, PGFR, IR. PD 0332991 is a non-ATP competitive inhibitor of Cdk4. PD 0332991 inhibits MDA-MB-435 breast carcinoma cells with IC50 of 66 nM, which is due to reduced Rb phosphorylation at Ser780. PD 0332991 inhibits thymidine incorporation into the DNA of Rb-positive human breast, colon, and lung carcinomas as well as human leukemias, with IC50 values ranging from 0.04-0.17 μM. PD 0332991 shows no activity in Rb-negative cells. PD 0332991 causes an accumulation of cells in G1 in MDA-MB-453 breast and Colo-205 carcinoma cells. [1] PD 0332991 also shows activity in 5T33MM myeloma cells (immunocompetent model) and sensitizes the cells to killing by bortezomib. [2] PD 0332991 inhibits luminal ER-positive as well as HER2-amplified breast cancer cell lines including MDA-MB-175, ZR-75-30, CAMA-1, MDA-MB-134, HCC-202 and UACC-893. PD 0332991 enhances the activity of tamoxifen and trastuzumab in these cell lines. PD 0332991 enhances the sensitivity of tamoxifen in the MCF7 tamoxifen-resistant cells. [3] A recent study shows that PD 0332991 could suppress malignant rhabdoid tumor (MRT) cell lines including MP-MRT-AN, KP-MRT-RY, G401, KP-MRT-NS and the sensitivity of the MRT cell lines to PD 0332991 is inversely correlated with expression of p16. [4]

Cell Data
 
Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
MOLM13 Kinase Assay   24 h   Inhibition of CDK4 assessed as inhibition of Rb phosphorylation with IC50 of 0.002 μM 24641103
COLO205 Growth Inhibition Assay   72 h   Antiproliferative activity assessed as incorporation of [3H]thymidine into DNA with IC50 of 0.036 μM 24641103
U937 Growth Inhibition Assay   72 h   Antiproliferative activity assessed as incorporation of [3H]thymidine into DNA with IC50 of 0.14 μM 24641103

... Click to View More Cell Line Experimental Data

Assay
Methods Test Index PMID
Western blot         30300583 28453226 30343527
Growth inhibition assay 29670090
Immunofluorescence   26988987 28453226
ELISA 26540629
In vivo PD 0332991 indicates complete tumor stasis in a MDA-MB-435 xenograft at 150 mg/kg. PD 0332991 also shows broad-spectrum antitumor activity in multiple human tumor xenografts by eliminating phospho-Rb and the proliferative marker Ki-67 from tumor tissue and down-regulation of genes under the transcriptional control of E2F. [1]

 

Details

Other products of this supplier

lookchemhot product CAS New CAS Cas Database Article Data Chemical Catalog