Furamidine dihydrochloride Datasheet DC Chemicals
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Cat.No DC11235
Name Furamidine dihydrochloride

Chemical Properties

CAS 55368-40-6
Formula C18H16N4O
MW 304.345843315125
Storage 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological activity

Description CAS NO.:55368-40-6
Product Name:Benzenecarboximidamide,4,4'-(2,5-furandiyl)bis-, dihydrochloride (9CI)
Synonyms:Benzenecarboximidamide,4,4'-(2,5-furandiyl)bis-, dihydrochloride (9CI);Furamidine Dihydrochloride;4-[5-(4-carbamimidoylphenyl)-2-furyl]benzenecarboximidamide;Benzenecarboximidamide, 4,4'-(2,5-furandiyl)bis-, dihydrochloride;2,5-Furandiylbis(1,4-phenylene)bisformamidine;DB75;DB-75;Furamidine;WR-199385;2,5-Bis(4-amidinophenyl)furan dihydrochloride;4,4′-(2,5-Furandiyl)bis-benzenecarboximidamide dihydrochloride;DB 75;NSC 305831;WR199385
EINEC:
Molecular Formula:C18H16N4O
Molecular Weight:304.345843315125
Target: IC50: 9.4 μM (Protein arginine methyltransferase 1 (PRMT1)); 166 µM (PRMT5), 283 µM (PRMT6) and >400 µM (PRMT4)[1] Parasite[1] Tyrosyl-DNA phosphodiesterase 1 (TDP-1)[2]
In Vivo Furamidine (1 mg/kg; intraperitoneal injection; 3 times a week and repeated every 4 weeks; for 34 weeks; female NZB/NZW mice) and Irinotecan combined treatment suppresses proteinuria and prolongs survival of lupus-prone NZB/NZW mice. The combination treatment does not change the levels of anti-dsDNA antibodies[3]. Animal Model: Female NZB/NZW mice (6-week-old) with Irinotecan (1 mg/kg)[3] Dosage: 1 mg/kg Administration: Intraperitoneal injection; 3 times a week and repeated every 4 weeks; for 34 weeks Result: Suppressed proteinuria and prolongs survival of lupus-prone NZB/NZW mice combined with Irinotecan.
In Vitro Furamidine (compound 1; 20 μM; 72 hours; leukemia cell lines) inhibits cell growth for most of the leukemia cell lines except HEL cells which have JAK2V617F mutations[1]. Furamidine (compound 1; 20 μM; 15 hours; 293T cells) treatment significantly reduces the expression level of the methylated GFP-ALY protein in 293T cells[1]. Furamidine binds duplex DNA in the DNA minor groove selectively at AT rich sites [(A/T)4]. Furamidine can also intercalate between GC base pairs of duplex DNA. Furamidine could therefore interfere with DNA processing enzymes such as TDP-1[2]. Cell Viability Assay[1] Cell Line: Meg-01, K562, HL-60, NB4, MOLM13, HEL, CMK, CMY, CMS and CHRF cells Concentration: 20 μM Incubation Time: 72 hours Result: Inhibited cell growth for most of the leukemia cell lines except HEL cells which have JAK2V617F mutations. Western Blot Analysis[1] Cell Line: 293T cells Concentration: 20 μM Incubation Time: 15 hours Result: The expression level of the methylated GFP-ALY protein is significantly reduced.
Kinase Assay
Cell Assay
Animal Administration

References

[1]. Yan L, et al. Diamidine compounds for selective inhibition of protein arginine methyltransferase 1. J Med Chem. 2014 Mar 27;57(6):2611-22. [2]. Antony S, et al. Novel high-throughput electrochemiluminescent assay for identification of human tyrosyl-DNA phosphodiesterase (Tdp1) inhibitors and characterization of furamidine (NSC 305831) as an inhibitor of Tdp1. Nucleic Acids Res. 2007;35(13):4474-84. [3]. Keil A, et al. The Topoisomerase I Inhibitor Irinotecan and the Tyrosyl-DNA Phosphodiesterase 1 Inhibitor Furamidine Synergistically Suppress Murine Lupus Nephritis. Arthritis Rheumatol. 2015 Jul;67(7):1858-67.
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