الصفحة الرئيسية>>Signaling Pathways>> Microbiology & Virology>> Parasite>>Furamidine (hydrochloride)

Furamidine (hydrochloride)

رقم الكتالوجGC43715

فوراميدين (هيدروكلوريد) (DB75 ثنائي هيدروكلوريد) هو مثبط انتقائي للبروتين أرجينين ميثيل ترانسفيراز 1 (PRMT1) مع IC50 من 9.4 μ ؛ M.

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Furamidine (hydrochloride) التركيب الكيميائي

Cas No.: 55368-40-6

الحجم السعر المخزون الكميّة
1mg
43٫00
متوفر
5mg
128٫00
متوفر
10mg
237٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Furamidine is a cell-permeable inhibitor of protein arginine methyltransferase 1 (PRMT1) that is selective for PRMT1 over PRMT5, PRMT6, and PRMT4/coactivator-associated arginine methyltransferase 1 (CARM1) (IC50s = 9.4, 166, 283, and >400 μM, respectively). In vitro, furamidine (20 μM) inhibits Aly protein methylation in HEK293T cells and growth of several leukemia cell lines. It inhibits tyrosyl-DNA phosphodiesterase (Tdp1) activity on both single- and double-stranded DNA substrates with concentrations in the low micromolar range, but it is more potent against a duplex DNA substrate. Furamidine inhibits growth of T. brucei, the parasite that causes sleeping sickness, with IC50 values of 1.5 to 37 nM across various strains. It inhibits the T. brucei P2 aminopurine transporter (Ki = 1.2 μM). It also binds to AT-rich DNA sequences in trypanosome kinetoplast DNA.

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