Powder: -20°C for 3 years | In solvent: -80°C for 1 year
BAY-299 is an effecitve inhibitor of the bromodomain and PHD finger family member BRPF2 and the TATA box binding protein-associated factors TAF1 and TAF1L with IC50s of 67 nM, 8 nM, and 106 nM, respectively.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
5 mg | In stock | $ 43.00 | |
10 mg | In stock | $ 70.00 | |
25 mg | In stock | $ 143.00 | |
50 mg | In stock | $ 253.00 | |
100 mg | In stock | $ 446.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 48.00 |
Description | BAY-299 is an effecitve inhibitor of the bromodomain and PHD finger family member BRPF2 and the TATA box binding protein-associated factors TAF1 and TAF1L with IC50s of 67 nM, 8 nM, and 106 nM, respectively. |
Targets&IC50 | BRPF2 BD:67 nM, BRPF3 BD:5550 nM, BRPF1 BD:3150 nM, TAF1L BD2:106 nM, TAF1 BD2:8 nM |
In vitro | BAY-299 inhibits the cells proliferation of NCI-H526, CHL-1, MOLM-13, MV4-11, 769-P, Jurkat, and 5637 with GI50s of 6860, 7400, 1060, 2630, 3210, 3900, and 7980 nM, respectively. BAY-299 blocks the interaction of BRPF2 BD with H4 and H3.3 with IC50s of 575 and 825 nM, respectively[1]. |
In vivo | The in vivo pharmacokinetic properties of BAY-299 in rats show are blood clearance is low (17% of hepatic blood flow), terminal half-life long to very long with t1/2 of 10 h, volume of distribution in steady-state high, and bioavailability high with F of 73%[1]. |
Synonyms | BAY299, BAY 299 |
Molecular Weight | 429.47 |
Formula | C25H23N3O4 |
CAS No. | 2080306-23-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 20 mg/mL (46.6 mM), Sonication and heating are recommended.
You can also refer to dose conversion for different animals. More
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BAY-299 2080306-23-4 Chromatin/Epigenetic Proteases/Proteasome Epigenetic Reader Domain Carboxypeptidase BAY299 BAY 299 inhibitor inhibit