>>Signaling Pathways>> Chromatin/Epigenetics>> Histone Methyltransferase>>A 366

A 366

Catalog No.GC16015

A 366은 G9a 및 GLP(EHMT1)에 대해 각각 3.3 및 38nM의 IC50을 갖는 강력하고 고도로 선택적인 펩티드 경쟁 히스톤 메틸트랜스퍼라제 G9a 억제제입니다. A 366은 21개의 다른 메틸트랜스퍼라제에 비해 \u003e1000배 선택성을 나타냅니다. A 366은 또한 Spindlin1-H3K4me3-상호작용의 강력한 나노몰 억제제입니다(IC50\u003d182.6nM). A 366은 인간 히스타민 H3 수용체(Ki\u003d17 nM)에서 높은 친화성을 나타내며 히스타민성 및 도파민성 수용체 패밀리의 하위 집합 중에서 하위 유형 선택성을 나타냅니다.

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A 366 Chemical Structure

Cas No.: 1527503-11-2

Size 가격 재고 수량
10mM (in 1mL DMSO)
US$38.00
재고 있음
10mg
US$74.00
재고 있음
50mg
US$283.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

A-366 is a potent histone methyltransferase G9a inhibitor with an IC50 of 3.3 nM.

References:
[1]. Pappano WN, et al. The Histone Methyltransferase Inhibitor A-366 Uncovers a Role for G9a/GLP in the Epigenetics of Leukemia.PLoS One. 2015 Jul 6;10(7):e0131716.

리뷰

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Average Rating: 5 ★★★★★ (Based on Reviews and 36 reference(s) in Google Scholar.)

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