FHT 2344

Pricing Availability   Qty
说明: Potent SMARCA2/4 inhibitor
化学名: N-[(1S)-1-(Methoxymethyl)-2-[[4-[3-(1-methyl-1H-pyrazol-3-yl)phenyl]-2-thiazolyl]amino]-2-oxoethyl]-1-(methylsulfonyl)-1H-pyrrole-3-carboxamide
纯度: ≥95% (HPLC)
说明书
引用文献
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文献 (4)

生物活性 for FHT 2344

FHT 2344 is a potent allosteric and ATP-competitive inhibitor of SMARCA2/SMARCA4 ATPases (also known as BRM/BRG1) of the BAF complex (IC50 values are 13.8 and 26.1 nM at SMARCA2 and SMARCA4, respectively). FHT 2344 inhibits SMARCA2 transcriptional activity in a BRG1-mutant cell line and SMARCA4 transcription in a BRM-mutant cell line (IC50 values are 29.8 and 30.2 nM, respectively). Dose-dependently reduces tumor growth in a uveal melanoma xenograft model and suppresses SOX10 transcription.

许可信息

Sold under license from Foghorn Therapeutics

技术数据 for FHT 2344

分子量 528.6
公式 C23H24N6O5S2
储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 2468058-90-2
InChI Key APLVGTKXOIMODQ-IBGZPJMESA-N
Smiles COC[C@@H](C(NC1=NC(C2=CC(C3=NN(C=C3)C)=CC=C2)=CS1)=O)NC(C4=CN(S(C)(=O)=O)C=C4)=O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for FHT 2344

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 26.43 50

制备储备液 for FHT 2344

以下数据基于产品分子量 528.6。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.5 mM 3.78 mL 18.92 mL 37.84 mL
2.5 mM 0.76 mL 3.78 mL 7.57 mL
5 mM 0.38 mL 1.89 mL 3.78 mL
25 mM 0.08 mL 0.38 mL 0.76 mL

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参考文献 for FHT 2344

参考文献是支持产品生物活性的出版物。

Centore et al (2021) Discovery of novel BAF inhibitors for the treatment of transcription factor-driven cancers. Cancer Res. 81 1224


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关键词: FHT 2344, FHT 2344 supplier, FHT2344, SMARCA, SMARCA2, SMARCA4, potent, inhibitor, inhibitors, BRM, BRG1, BAF, complex, transcription, tumour, tumor, uveal, melanoma, xenograft, SOX10, Bromodomains, Other, ATPases, 7645, Tocris Bioscience

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