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  • DC Chemicals Limited
  • China
  • Product Name: PK11000
  • Price: $300.0/100mg $600.0/250mg $1200.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

Related CAS#:

38275-34-2

38275-34-2 structure
38275-34-2 structure
  • Name: PK11007
  • Chemical Name: 5-chloro-2-methylsulfonylpyrimidine-4-carboxylic acid
  • CAS Number: 38275-34-2
  • Molecular Formula: C6H5ClN2O4S
  • Molecular Weight: 236.63300
  • Catalog: Signaling Pathways Apoptosis MDM-2/p53
  • Create Date: 2019-01-02 18:23:12
  • Modify Date: 2024-01-13 11:28:55
  • PK11007 is a p53 targeting compound, has anti-tumor activities through activation of unstable p53.

Name 5-chloro-2-methylsulfonylpyrimidine-4-carboxylic acid
Synonyms 2-methanesulfonyl-5-chloro-4-pyrimidinecarboxylic acid
2-methylsulfonyl-5-chloro-4-pyrimidine carboxylic acid
2-methylsulfonyl-5-chloropyrimidine-4-carboxylic acid
5-chloro-2-methanesulfonyl-pyrimidine-4-carboxylic acid
4-carboxy-5-chloro-2-methylsulfonylpyrimidine
PK11007
Description PK11007 is a p53 targeting compound, has anti-tumor activities through activation of unstable p53.
Related Catalog
Target

p53[1]

In Vitro PK11007 (15-30 µM) reduces the viability of mutant p53 cell lines MKN1 (V143A), HUH-7 (Y220C), NUGC-3 (Y220C), and SW480 (R273H/P309S). PK11007 also shows inhibitory activities against the p53 wt cancer cell lines HUH-6 and NUGC-4, as well as the fibroblast cell line WI-38 only at high concentrations (60 and 120 µM). PK11007 increases levels of p53 target genes and activates the unfolded protein response pathway. PK11007 also increases p53 activity in HUH-6 and NUGC-4 cells. PK11007 induces cell death via caspase-independent pathways. PK11007 (30, 60 µM) induces reactive oxygen species (ROS) especially in mutant p53 cells[1]. PK11007 inhibits the proliferation of a panel of 17 breast cell lines, with IC50s ranging from 2.3 to 42.2 μM[2].
Cell Assay Cell viability is measured using the CellTiter-Fluor cell viability assay kit. Cells are seeded in 96-well plates at 7,500-15,000 cells per well and incubated overnight. Samples are prepared in medium with a twice-as-high compound (including PK11007), and DMSO concentration then added to an equivalent volume of growth medium, yielding a final DMSO concentration of 0.5%. After incubating of cells for 23 h or the respective time period, CellTiter-Fluor reagent is added to each well and incubated again for 45 min. Fluorescence is then recorded on a PHERAstar plate reader using 400/500 nm excitation/emission filters. Experiments are performed in quadruplicate[1].
References

[1]. Bauer MR, et al. 2-Sulfonylpyrimidines: Mild alkylating agents with anticancer activity toward p53-compromised cells. Proc Natl Acad Sci U S A. 2016 Sep 6;113(36):E5271-80.

[2]. Synnott NC, et al. Mutant p53 as a therapeutic target for the treatment of triple-negative breast cancer: Preclinical investigation with the anti-p53 drug, PK11007. Cancer Lett. 2018 Feb 1;414:99-106

Molecular Formula C6H5ClN2O4S
Molecular Weight 236.63300
Exact Mass 235.96600
PSA 105.60000
LogP 1.31250
Storage condition -20℃
HS Code 2933599090
Precursor  1

DownStream  1

HS Code 2933599090
Summary 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%