Kartogenin

Pricing Availability   Qty
说明: Potently induces chondrogenesis in MSCs
化学名: 2-[((1,1'-Biphenyl)-4-ylamino)carbonyl]benzoic acid
纯度: ≥98% (HPLC)
说明书
引用文献
评论 (1)
文献 (4)

生物活性 for Kartogenin

Kartogenin potently induces differentiation of human mesenchymal stem cells into chondrocytes (EC50 = 100 nM). Reduces disease severity in a mouse model of osteoarthritis; displays protective effects against osteoarthritic stimuli in mature chondrocytes in vitro.

化合物库 for Kartogenin

Kartogenin is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen Stem Cell Library. 了解 Tocris 化合物库的更多信息。

技术数据 for Kartogenin

分子量 317.34
公式 C20H15NO3
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 4727-31-5
PubChem ID 2826191
InChI Key SLUINPGXGFUMLL-UHFFFAOYSA-N
Smiles O=C(NC2=CC=C(C3=CC=CC=C3)C=C2)C1=CC=CC=C1C(O)=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 Kartogenin

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 31.73 100
ethanol 15.87 50

制备储备液 for Kartogenin

以下数据基于产品分子量 317.34。 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 31.51 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 Kartogenin

参考文献是支持产品生物活性的出版物。

Johnson et al (2012) A stem cell-based approach to cartilage repair. Science 336 717 PMID: 22491093


If you know of a relevant reference for Kartogenin, please let us know.

关键词: Kartogenin, Kartogenin supplier, Supplier, mesenchymal, stem, cell, differentiation, differentiators, potently, inducers, chondrocytes, cartilage, osteoarthritis, Mesenchymal, Stem, Cells, 4513, Tocris Bioscience

篇 Kartogenin 的引用文献

引用文献是使用了 Tocris 产品的出版物。

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Kartogenin 的评论

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Chondrogenic differentiation of human bone marrow stromal cells.
By Nicola Foster on 08/28/2020
分析类型: In Vitro
种属: Human

Added to culture medium on days 1-3 at 10 µM to induced chondrogenic differentiation in an immortalized hBMSC cell line. After 7 days there was increased sulfated GAG production compared to basic controls and increased DNA yield compared to cells cultured in traditional chondrogenic differentiation medium.

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该领域的文献

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