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CPI-455, KDM5 Demethylases Inhibitor

CPI-455, KDM5 Demethylases Inhibitor

$129.00
A potent and selective KDM5A inhibitor.
Catalog No. Unit Price Qty
M60326-2s 2 mg solid $129.00

Details

Product Information
Molecular Weight: 278.32
Formula: C16H14N4O
Purity: ≥98%
CAS#: 1628208-23-0
Solubility: DMSO up to 50 mM
Chemical Name: 6-isopropyl-7-oxo-5-phenyl-4,7-dihydropyrazolo[1,5-a]pyrimidine-3-carbonitrile
Storage: Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.

Biological Activity:

CPI-455 is a potent and selective KDM5A inhibitor with IC50 ~10 nM. It inhibits KDM5A, KDM5B and KDM5C to similar extents but showed substantially weaker potency toward KDM4C and KDM7B (~200- and 770-fold, respectively) and no measurable inhibition of KDM2B, KDM3B or KDM6A. It specifically alters H3K4 methylation in cells and binds at the demethylase active site. CPI-455 mediated KDM5 inhibition, elevated global levels of H3K4 trimethylation (H3K4me3) and decreased the number of DTPs in multiple cancer cell line models treated with standard chemotherapy or targeted agents.

How to Use:

In vitro:
KDM5-C70 was used at 1-10 µM in vitro and cellular assays.
In vivo: n/a

Reference:

  • 1. Vinogradova M, et al. An inhibitor of KDM5 demethylases reduces survival of drug-tolerant cancer cells. (2016) Nat Chem Biol. 12(7):531-8.


CPI-455_spec.pdf     
CPI-455_MSDS.pdf 


Products are for research use only. Not for human use. 

Description

Details

Product Information
Molecular Weight: 278.32
Formula: C16H14N4O
Purity: ≥98%
CAS#: 1628208-23-0
Solubility: DMSO up to 50 mM
Chemical Name: 6-isopropyl-7-oxo-5-phenyl-4,7-dihydropyrazolo[1,5-a]pyrimidine-3-carbonitrile
Storage: Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.

Biological Activity:

CPI-455 is a potent and selective KDM5A inhibitor with IC50 ~10 nM. It inhibits KDM5A, KDM5B and KDM5C to similar extents but showed substantially weaker potency toward KDM4C and KDM7B (~200- and 770-fold, respectively) and no measurable inhibition of KDM2B, KDM3B or KDM6A. It specifically alters H3K4 methylation in cells and binds at the demethylase active site. CPI-455 mediated KDM5 inhibition, elevated global levels of H3K4 trimethylation (H3K4me3) and decreased the number of DTPs in multiple cancer cell line models treated with standard chemotherapy or targeted agents.

How to Use:

In vitro:
KDM5-C70 was used at 1-10 µM in vitro and cellular assays.
In vivo: n/a

Reference:

  • 1. Vinogradova M, et al. An inhibitor of KDM5 demethylases reduces survival of drug-tolerant cancer cells. (2016) Nat Chem Biol. 12(7):531-8.


CPI-455_spec.pdf     
CPI-455_MSDS.pdf 


Products are for research use only. Not for human use. 

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