Description
A cell-permeable inhibitor with selectivity for PRMT1 (IC50 = 9.4 μM) over PRMT5, PRMT6, and PRMT4/CARM1 (IC50s = 166, 283, and >400 μM, respectively); inhibits Aly protein methylation in HEK293T cells and growth of several leukemia cell lines when used at a concentration of 20 μM; inhibits Tdp1 activity on single- and double-stranded DNA with concentrations in the low micromolar range; inhibits T. brucei (IC50 values of 1.5 to 37 nM across various strains); inhibits the T. brucei P2 aminopurine transporter (Ki = 1.2 μM); binds to AT-rich DNA sequences,
Formal name: 4,4′-(2,5-furandiyl)bis-benzenecarboximidamide, dihydrochloride
Synonyms:
Molecular weight: 377.3
CAS: 55368-40-6
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Antiparasitics|Antiprotozoals||Product Type|Biochemicals|Small Molecule Inhibitors|Methyltransferases||Research Area|Epigenetics, Transcription, & Translation|Writers||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Parasitic Diseases|African Sleeping Sickness