RAF709
Important Notice: For research use only. We do not sell to patients.
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Important Notice: For research use only. We do not sell to patients.
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Discription | RAF709 is a potent inhibitor of B/C RAF kinase with almost equivalent IC50 values of 0.4 nM for B-RAF and C-RAF, showing a high level of selectivity, demonstrating greater than 99% on-target binding to BRAF, BRAFV600E, and CRAF at 1 μM and very few off-targets with DDR1 (>99%), DDR2 (86%), FRK (92%), and PDGFRb (96%), the only kinases with binding >80% at 1 μM. | ||
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Targets |
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Catalog Num | A16842 |
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Formula | C28H29F3N4O4 |
Molecular Weight | 542.55 |
CAS Number | 1628838-42-5 |
SMILES | O=C(NC1=CN=C(C)C(C2=CC(N3CCOCC3)=C(OC4CCOCC4)N=C2)=C1)C5=CC(C(F)(F)F)=CC=C5 |
Synonyms | RAF 709, RAF-709 |
Storage | Store lyophilized at -20ºC, keep desiccated. |
In vitro | DMSO | 86 mg/mL (158.51 mM) | |
Water | Insoluble | ||
Ethanol | 86 mg/mL (158.51 mM) | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
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0.1 mM | 18.43 mL | 92.16 mL | 184.31 mL |
0.5 mM | 3.69 mL | 18.43 mL | 36.86 mL |
1 mM | 1.84 mL | 9.22 mL | 18.43 mL |
5 mM | 0.37 mL | 1.84 mL | 3.69 mL |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2