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Ralaniten (Synonyms: EPI-002)

Catalog No.GC62683

Ralaniten(EPI-002)은 안드로겐 수용체-N-말단 도메인(AR-NTD)의 강력하고 경구 활성 길항제입니다. Ralaniten은 7.4μM의 IC50으로 AR 전사 활성을 억제합니다. Ralaniten은 거세저항성 전립선암(CRPC) 연구에 사용할 수 있습니다.

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Ralaniten Chemical Structure

Cas No.: 1203490-23-6

Size 가격 재고 수량
10mM(in 1mL DMSO)
US$99.00
재고 있음
5mg
US$90.00
재고 있음
10mg
US$144.00
재고 있음
25mg
US$288.00
재고 있음
50mg
US$450.00
재고 있음
100mg
US$720.00
재고 있음

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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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Average Rating: 5 ★★★★★ (Based on Reviews and 29 reference(s) in Google Scholar.)

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