PKUMDL WQ 2101

Pricing Availability   Qty
说明: Negative allosteric modulator of 3-phosphoglycerate dehydrogenase (PHGDH)
化学名: 2,4-Dihydroxy-N'-(2-hydroxy-5-nitrobenzylidene)benzohydrazide
纯度: ≥98% (HPLC)
说明书
引用文献 (1)
评论
文献 (2)

生物活性 for PKUMDL WQ 2101

PKUMDL WQ 2101 is a negative allosteric modulator of phosphoglycerate dehydrogenase (PHGDH) (IC50 = 34.8 μM). Exhibits antitumor activity in vitro in breast cancer cells lines overexpressing PHGDH (EC50 values are 7.7 and 10.8 μM in MDA-MB-468 and HCC-70 cells, respectively). Inhibits growth of MDA-MB-468 xenografts in mice.

技术数据 for PKUMDL WQ 2101

分子量 317.25
公式 C14H11N3O6
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 304481-72-9
PubChem ID 6741780
InChI Key RABUUVVWWJCYEN-UHFFFAOYSA-N
Smiles OC1=CC(O)=C(C(N/N=C/C2=CC([N+]([O-])=O)=CC=C2O)=O)C=C1

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 PKUMDL WQ 2101

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 31.73 100

制备储备液 for PKUMDL WQ 2101

以下数据基于产品分子量 317.25。 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
1 mM 3.15 mL 15.76 mL 31.52 mL
5 mM 0.63 mL 3.15 mL 6.3 mL
10 mM 0.32 mL 1.58 mL 3.15 mL
50 mM 0.06 mL 0.32 mL 0.63 mL

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参考文献 for PKUMDL WQ 2101

参考文献是支持产品生物活性的出版物。

Wang et al (2017) Rational design of selective allosteric inhibitors of PHGDH and serine synthesis with anti-tumor activity. Cell Chem.Biol. 24 55 PMID: 28042046


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关键词: PKUMDL WQ 2101, PKUMDL WQ 2101 supplier, PKUMDLWQ2101, Phosphoglycerate, dehydrogenase, PHGDH, allosteric, inhibitor, serine, biosynthesis, negative, modulator, NAM, Other, Dehydrogenases, 6580, Tocris Bioscience

1 篇 PKUMDL WQ 2101 的引用文献

引用文献是使用了 Tocris 产品的出版物。 PKUMDL WQ 2101 的部分引用包括:

John M et al (2022) Purine nucleotide depletion prompts cell migration by stimulating the serine synthesis pathway. Nat Commun 13 2698 PMID: 35577785


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