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Arylquin 1

A Par-4 secretagogue

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Arylquin 1的二维码
  • 库存: 现货
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  • 1mg
    ¥537.00
    430.00
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  • 5mg
    ¥1837.00
    1470.00
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  • 10mg
    ¥3125.00
    2500.00
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  • 货号: ajci4322
  • CAS: 1630743-73-5
  • 别名:
  • 分子式: C17H16FN3
  • 分子量: 281.3
  • 纯度: >98%
  • 溶解度: DMSO: 20 mg/ml
  • 储存: Store at -20°C
  • 库存: 现货

Background

Arylquin 1 is a potent secretagogue of the tumor suppressor protein prostate apoptosis response-4 (Par-4).


Par-4 is ubiquitously expressed in normal cells and tissues, but it is inactivated, downregulated or mutated in several types of cancers. Par-4 can selectively induce cancer cell apoptosis but not normal cells. Both intracellular and secreted Par-4 have a role in apoptosis induction by caspase-dependent mechanisms.


In vitro: Previous study showed that Arylquin 1 produced a dose-dependent secretion in MEF cells and also induced robust secretion of Par-4 in normal or immortalized human cells but failed to induce the secretion of Par-4 in various lung tumor cells. Moreover, it was found that Brefeldin A, which blocked anterograde endoplasmic reticulum–Golgi traffic, could inhibit basal and Arylquin 1–inducible Par-4 secretion, indicating that Arylquin 1 regulated Par-4 secretion through the classical secretory pathway. In addition, cells treated with Arylquin 1 showed neither Par-4 co-immunoprecipitation nor colocalization with vimentin, suggesting that Arylquin 1 could displace Par-4 from vimentin. This action of Arylquin 1 was not associated with inhibition of vimentin expression, demonstrating that Arylquin 1 might cause conformational changes in vimentin to block its ability to bind and sequester Par-4 [1].


In vivo: So far, there is no animal in vivo data reported.


Clinical trial: Up to now, Arylquin 1 is still in the preclinical development stage.

Reference:
[1] Burikhanov R et al.? Arylquins target vimentin to trigger Par-4 secretion for tumor cell apoptosis. Nat Chem Biol. 2014 Nov;10(11):924-6.

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