CBX2-IN-1
CBX2-IN-1 is a CBX2 inhibitor with an IC50 of 9.6 μM. CBX2-IN-1 binds the CBX2 chromodomain’s H3K27me3 binding channel, blocks interaction between CBX2 and H3K27me3, and exhibits selective affinity toward CBX2, CBX4, CBX6, CBX7, and CBX8 over CBX1, CBX3, and CBX5. CBX2-IN-1 can be used for the research of prostate cancers.
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- Formule: C29H27N3O3
- Masse moléculaire:465.54
-
Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Activité biologique
-
Chemical Information
- Pureté et documentation
- Références
-
Help & FAQs
Voir tous les produits spécifiques à Isoform Histone Methyltransferase
More
Activité biologique
|
CBX2 9.6 μM (IC50) |
CBX2-IN-1 (compound 37) (50 μM) inhibits CBX2 in the NanoBRET assay with an IC50 of 9.6 μM, showing key interactions with the CBX2 chromodomain’s aromatic cage and Asp51 residue[1].
CBX2-IN-1 likely exhibits selective affinity for CBX2 and closely related isoforms (CBX4, CBX6, CBX7, CBX8) over CBX1, CBX3, and CBX5 due to conserved binding interactions and sequence identity[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
Masse moléculaire 465.54
-
Formule C29H27N3O3
-
SMILES
COC1=CC=CC=C1NC(C2=CC=C(C=C2)NC(CC3=CC=C(C=C3)NCC4=CC=CC=C4)=O)=O
-
Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
CBX2-IN-1 Related Classifications
HY-181089 Related Classifications
Powered by Bioz