CBP/p300-IN-10

Modify Date: 2024-04-08 19:44:32

CBP/p300-IN-10 Structure
CBP/p300-IN-10 structure
Common Name CBP/p300-IN-10
CAS Number 2259641-71-7 Molecular Weight 537.48
Density N/A Boiling Point N/A
Molecular Formula C25H24F5N5O3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of CBP/p300-IN-10


CBP/p300-IN-10 is a highly potent histone acetyltransferase EP300 and CREBBP with IC50 values of 26 nM and 39 nM, respectively. CBP/p300-IN-10 can be used to research anticancer[1].

 Names

Name CBP/p300-IN-10

 CBP/p300-IN-10 Biological Activity

Description CBP/p300-IN-10 is a highly potent histone acetyltransferase EP300 and CREBBP with IC50 values of 26 nM and 39 nM, respectively. CBP/p300-IN-10 can be used to research anticancer[1].
Related Catalog
Target

EP300:26 nM (IC50)

CREBBP:39 nM (IC50)

In Vitro CBP/p300-IN-10 (example 84) (0-1 μM; 3 h) inhibit H3K27Ac activity in LK2 cells with an IC50 of 22 nM[1]. CBP/p300-IN-10 (38 nM-10 mM; 3 days) has inhibitory activity against LK2 and TE-8[1]. Cell Proliferation Assay[1] Cell Line: LK2 and TE-8 Concentration: 38 nM-10 mM Incubation Time: 3 days Result: Inhibited LK2 and TE-8 with GI50s of 97.163 nM and 152.484 nM, respectively.
References

[1]. Naito, Hiroyuki, et al. Preparation of amino acid amide derivatives such as L- and D-prolinamide derivatives as Ep300/CREBBP inhibitors. WO2018235966A1

 Chemical & Physical Properties

Molecular Formula C25H24F5N5O3
Molecular Weight 537.48