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Key Documents

557403

Sigma-Aldrich

RNA 聚合酶 III抑制剂

RNA Polymerase III Inhibitor, CAS 577784-91-9, is a cell-permeable inhibitor of RNA Polymerase III (IC₅₀ = 27 and 32 µM for human and S. cerevisiae RNA Pol III, respectively).

别名:

RNA 聚合酶 III抑制剂, ML-60218,N-[1-(3-(5-氯-3-甲基苯并[b]噻吩-2-基-1-甲基-1H-吡唑-5-基)]-2-氯苯磺酰胺

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About This Item

经验公式(希尔记法):
C19H15Cl2N3O2S2
分子量:
452.38
分類程式碼代碼:
12352200
NACRES:
NA.54

品質等級

化驗

≥95% (HPLC)

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

off-white

溶解度

DMSO: 15 mg/mL

運輸包裝

ambient

儲存溫度

2-8°C

InChI

1S/C19H15Cl2N3O2S2/c1-11-13-9-12(20)7-8-16(13)27-19(11)15-10-18(24(2)22-15)23-28(25,26)17-6-4-3-5-14(17)21/h3-10,23H,1-2H3

InChI 密鑰

BVBDTTLISMIOJY-UHFFFAOYSA-N

一般說明

RNA聚合酶III(RNA Pol III)的细胞可渗透性抑制剂(对于人RNA Pol III的IC50=27 µM,对于酿酒酵母的RNA Pol III的IC50=32 µM)。通过阻止RNA Pol III介导的tRNA转录,来抑制酵母中的细胞生长。
一种对RNA聚合酶III具有广谱抑制活性的细胞可渗透性吲唑磺酰胺化合物(对于人和酿酒酵母RNA Pol III分别为IC50 = 27和32 µM)。通过阻止RNA Pol III介导的tRNA转录,来抑制酵母中的细胞生长。也可以25 mM的DMSO溶液(目录号557404)提供。

生化/生理作用

产物不与ATP竞争。
可逆:否
抗RNA聚合酶III的主要靶标
活性
细胞可渗透性:是
靶标IC50:对于人为27M,对于酿酒酵母RNA Pol III为32 µM

包裝

用惰性气体包装

警告

毒性:致癌/致畸(D)

準備報告

可能需要稍微加热才能完全溶解。

重構

复溶后,等分并冷冻保存(-20°C)。贮备溶液在-20°C下可稳定保存至多3个月。

其他說明

Wu, L., et al. 2003.Euk.Cell2, 256.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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RNA biology, 8(3), 496-505 (2011-05-03)
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Although central to evolution, the causes of hybrid inviability that drive reproductive isolation are poorly understood. Embryonic lethality occurs when the eggs of the frog X. tropicalis are fertilized with either X. laevis or X. borealis sperm. We observed that distinct subsets of
Kevin Van Bortle et al.
Nature communications, 13(1), 3007-3007 (2022-06-01)
RNA polymerase III (Pol III) includes two alternate isoforms, defined by mutually exclusive incorporation of subunit POLR3G (RPC7α) or POLR3GL (RPC7β), in mammals. The contributions of POLR3G and POLR3GL to transcription potential has remained poorly defined. Here, we discover that
Sijie Liu et al.
Cell, 184(5), 1314-1329 (2021-02-25)
End resection in homologous recombination (HR) and HR-mediated repair of DNA double-strand breaks (DSBs) removes several kilobases from 5' strands of DSBs, but 3' strands are exempted from degradation. The mechanism by which the 3' overhangs are protected has not

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