B02
Tocris Bioscience, part of Bio-Techne | Catalog # 6392
RAD51 recombinase inhibitor
Key Product Details
Description
RAD51 recombinase inhibitor
Product Description
B02 is a RAD51 recombinase inhibitor, exhibiting selectivity for human RAD51 over the E.coli homologue RecA (IC50 values are 27.4 μM and >250 μM, respectively). Inhibits homologous recombination and increases cellular sensitivity to DNA damage in vitro. Enhances the therapeutic effect of cisplatin (Cat. No. 2251) on tumor cells in vivo.Product Specifications
Molecular Weight
339.40
Formula
C22H17N3O
Storage
Store at +4°C
Purity
≥98% (HPLC)
Chemical Name
3-(Phenylmethyl)-2-[(1E)-2-(3-pyridinyl)ethenyl]-4(3H)-quinazolinone
CAS Number
1290541-46-6
PubChem ID
5738263
InChI Key
GEKDQXSPTHHANP-OUKQBFOZSA-N
SMILES
O=C1N(CC2=CC=CC=C2)C(/C=C/C3=CN=CC=C3)=NC4=CC=CC=C41
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 33.94 | 100 | |
| Ethanol | 3.39 | 10 |
Preparing Stock Solutions
for B02
The following data is based on the product molecular weight 339.40
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.95 mL | 14.73 mL | 29.46 mL |
| 5 mM | 0.59 mL | 2.95 mL | 5.89 mL |
| 10 mM | 0.29 mL | 1.47 mL | 2.95 mL |
| 50 mM | 0.06 mL | 0.29 mL | 0.59 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Huang and Mazin A small molecule inhibitor of human RAD51 potentiates breast cancer cell killing by therapeuticagents in mouse xenografts. PLoS One 2014 PMID: 24971740
- Huang Inhibition of homologous recombination in human cells by targeting RAD51 recombinase. J.Med.Chem. 2012 PMID: 22380680
- Alagpulinsa A small-molecule inhibitor of RAD51 reduces homologous recombination and sensitizes multiple myeloma cells to dox. Front.Oncol. 2014 PMID: 25401086
- Huang Identification of specific inhibitors of human RAD51 recombinase using high-throughputscreening. ACS Chem.Biol. 2011 PMID: 21428443
Product Specific Notices for B02
For research use only
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