الصفحة الرئيسية>>Signaling Pathways>> Endocrinology and Hormones>> Androgen Receptor>>Ralaniten

Ralaniten (Synonyms: EPI-002)

رقم الكتالوجGC62683

Ralaniten (EPI-002) هو مضاد قوي وفعال عن طريق الفم لمجال مستقبلات الأندروجين- N- الطرفية (AR-NTD)Ralaniten يثبط نشاط النسخ AR ، مع IC من 7.4 ميكرومتريمكن استخدام رالانيتن في البحث عن سرطان البروستاتا المقاوم للإخصاء (CRPC)

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Ralaniten التركيب الكيميائي

Cas No.: 1203490-23-6

الحجم السعر المخزون الكميّة
10mM(in 1mL DMSO)
99٫00
متوفر
5mg
90٫00
متوفر
10mg
144٫00
متوفر
25mg
288٫00
متوفر
50mg
450٫00
متوفر
100mg
720٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

Ralaniten (EPI-002) is a potent and orally active antagonist of the androgen receptor-N-terminal domain (AR-NTD). Ralaniten inhibits AR transcriptional activity, with IC50 of 7.4 μM. Ralaniten can be used for the research of castration-resistant prostate cancer (CRPC)[1][2].

EPI-002 (5-35 μM; 2-3 days) reduces AR-dependent proliferation of LNCaP cells, and has no effect on the viability of PC3 human prostate cancer cells that do not express functional AR[1].Ralaniten (10-35 μM; 4 h) inhibits transactivation of the AR N-terminal domain (NTD) induced by forskolin in LNCaP cells[1].

EPI-002 (100 mg/kg; p.o. twice daily for 28 days) inhibits the VCaP tumor growth in castrated mice[1].

[1]. Myung JK, et, al. An androgen receptor N-terminal domain antagonist for treating prostate cancer. J Clin Invest. 2013 Jul;123(7):2948-60.
[2]. Yang YC, et, al. Targeting Androgen Receptor Activation Function-1 with EPI to Overcome Resistance Mechanisms in Castration-Resistant Prostate Cancer. Clin Cancer Res. 2016 Sep 1;22(17):4466-77.

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