Furamidine dihydrochloride
Chemical Name: 4,4'-(2,5-Furandiyl)bis-benzenecarboximidamide dihydrochloride
Purity: ≥98%
Biological Activity
Furamidine dihydrochloride is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor (IC50 = 9.4 μM). Exhibits selectivity over PRMT5, PRMT6 and CARM1 (IC50 values are 166, 283 and >400 μM respectively). Inhibits tyrosyl-DNA phosphodiesterase 1 (TDP-1) (IC50 = 1.2 μM). Inhibits cell proliferation in leukemia cell lines, suppresses neuroblastoma tumor growth, and reduces mis-splicing in in vitro and in vivo models of myotonic dystrophy type 1. Also shows dose-dependent inhibition of platelet aggregation (IC50 = 14.8 uM). Cell-permeable.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Diamidine compounds for selective inhibition of protein arginine methyltransferase 1.
Yan et al.
J.Med.Chem., 2014;57:2611
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Citations for Furamidine dihydrochloride
The citations listed below are publications that use Tocris products. Selected citations for Furamidine dihydrochloride include:
5 Citations: Showing 1 - 5
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A genome-scale CRISPR screen reveals PRMT1 as a critical regulator of androgen receptor signaling in prostate cancer.
Authors: Tang Et al.
Cell Rep. 2022;38:110417
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PRMT1 is an important factor for medulloblastoma cell proliferation and survival.
Authors: Jer-Yen Et al.
Biochem Biophys Rep 2022;32:101364
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Inhibition of Arginine Methylation Impairs Platelet Function.
Authors: Marsden Et al.
ACS Pharmacol.Transl.Sci 2021;4:1567
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TC-E 5003, a protein methyltransferase 1 inhibitor, activates the PKA-dependent thermogenic pathway in primary murine and human subcutaneous adipocytes.
Authors: Min-Jung Et al.
FEBS Lett 2020;594:2923-2930
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Inhibiting Arginine Methylation as a Tool to Investigate Cross-Talk with Methylation and Acetylation Post-Translational Modifications in a Glioblastoma Cell Line.
Authors: Samuel Et al.
Proteomes 2018;6:44
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