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FX1

A potent, specific BCL6 BTB domain inhibitor with Kd of 7 uM, binds with a greater affinity than the natural BCL6 ligand SMRT (Kd=30 uM) ; exhibits 10-fold greater inhibitory activity against the BCL6 BTB domain in reporter assays with IC50 of 35 uM, displays good selectivity against a panel of 50 different kinases; disrupts formation of the BCL6 repression complex, reactivates BCL6 target genes, suppresses ABC-DLBCL cells in vitro and in vivo, as well as primary human ABC-DLBCL specimens ex vivo.

Product Specifications

CAS Number

1426138-42-2

Product Name Alternative

FX-1 | FX 1 | BCL6 inhibitor FX1

Purity

>98% (HPLC)

Solubility

DMSO: 30 mg/mL, Need Ultrasonic (< 1 mg/ml refers to the product slightly soluble or insoluble)

Smiles

O=C (O) CCN (C/1=O) C (SC1=C2C (NC3=C/2C=C (Cl) C=C3) =O) =S

Molecular Formula

C14H9ClN2O4S2

Molecular Weight

368.806

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

(Z) -3- (5- (5-chloro-2-oxoindolin-3-ylidene) -4-oxo-2-thioxothiazolidin-3-yl) propanoic acid

Available Sizes

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