الصفحة الرئيسية>>Signaling Pathways>> Ubiquitination/ Proteasome>> Autophagy>>AGN 194310

AGN 194310 (Synonyms: VTP-194310)

رقم الكتالوجGC12598

AGN 194310 (VTP-194310) هو عامل تقارب عالي ، قوي وانتقائي لمستقبلات حمض الريتينويك (RARs) مع قيم Kd تبلغ 3 نانومتر ، 2 نانومتر ، 5 نانومتر لـ RARα ، RARβ ، RARγ ، على التوالي

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AGN 194310 التركيب الكيميائي

Cas No.: 229961-45-9

الحجم السعر المخزون الكميّة
1mg
135٫00
متوفر
5mg
495٫00
متوفر
10mg
765٫00
متوفر
25mg
1305٫00
متوفر
50mg
2025٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

AGN 194310 is a pan-antagonist of retinoic acid receptors (RARs) with Kd values of 3nM, 2nM and 5nM for RAR α, RARβ and RARγ, respectively [1].

AGN 194310 has been reported to bind to RARs with equal and high Kd values of 3, 2 and 5nM for RAR α, RARβ and RARγ, respectively, by in vitro binding experiments. In addition, AGN 194310 has been revealed to potently inhibit the colony formation by ITS+-grown cell lines with IC50 values of 16 ± 5nM for LNCaP cells; 18 ± 6nM for PC3 cells; and 34 ± 7nM for DU-145 cells. Apart from these, because of binding to and mediating the effects via RARs, AGN 194310 has been demonstrated to inhibit agonist-induced (TTNPB) differentiation of HL60 cells. AGN 194310 has also shown the accumulation of cell in G1 and the function of induced apoptosis [1].

References:
[1] Hammond LA1, Van Krinks CH, Durham J, Tomkins SE, Burnett RD, Jones EL, Chandraratna RA, Brown G. Antagonists of retinoic acid receptors (RARs) are potent growth inhibitors of prostate carcinoma cells.Br J Cancer. 2001 Aug 3; 85(3):453-62.

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