Comparison

BAZ2-ICR European Partner

Item no. HY-19336-500mg
Manufacturer MedChem Express
CASRN 1665195-94-7
Amount 500 mg
Quantity options 100 mg 10 mM/1 mL 10 mg 1 g 1 mg 200 mg 25 mg 2 g 500 mg 50 mg 5 mg
Category
Type Inhibitors
Specific against other
Purity 99.95
Citations [1]Drouin L, et al. Structure enabled design of BAZ2-ICR, a chemical probe targeting the bromodomains of BAZ2A and BAZ2B. J Med Chem. 2015 Mar 12;58(5):2553-9.
Smiles N#CC1=CC=C(C2=C(C3=CN(C)N=C3)N=CN2CCC4=CN(C)N=C4)C=C1
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias 1665195-94-7
Similar products 1665195-94-7
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Applications
Cancer-programmed cell death
Manufacturer - Targets
Epigenetic Reader Domain
Shipping Temperature
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Molecular Weight
357.41
Product Description
BAZ2-ICR is a potent, selective, cell active and orally active BAZ2A/B bromodomains inhibitor with IC50s of 130 nM and 180 nM, and Kds of 109 nM and 170 nM, respectively. BAZ2-ICR shows 10-15-fold selectivity for binding BAZ2A/B over CECR2 and >100-fold selectivity over all other bromodomains. BAZ2-ICR is an epigenetic chemical probe[1].
Manufacturer - Research Area
Cancer
Solubility
DMF: 20 mg/mL (ultrasonic; warming)|DMSO: 10 mg/mL (ultrasonic; warming)
Manufacturer - Pathway
Epigenetics
Clinical information
No Development Reported

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 500 mg
Available: In stock
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