Acyl derivatives of p-aminosulfonamides and dapsone as new inhibitors of the arginine methyltransferase hPRMT1

…, A Eberlin, E Metzger, V Cura, P Hassenboehler…

Index: Bissinger, Elisabeth-Maria; Heinke, Ralf; Spannhoff, Astrid; Eberlin, Adrien; Metzger, Eric; Cura, Vincent; Hassenboehler, Pierre; Cavarelli, Jean; Schuele, Roland; Bedford, Mark T.; Sippl, Wolfgang; Jung, Manfred Bioorganic and Medicinal Chemistry, 2011 , vol. 19, # 12 p. 3717 - 3731

Full Text: HTML

Citation Number: 56

Abstract

Arginine methylation is an epigenetic modification that receives increasing interest as it plays an important role in several diseases. This is especially true for hormone-dependent cancer, seeing that histone methylation by arginine methyltransferase I (PRMT1) is involved in the activation of sexual hormone receptors. Therefore, PRMT inhibitors are potential drugs and interesting tools for cell biology. A dapsone derivative called allantodapsone ...

Related Articles:

Design, synthesis, and biological evaluation of a series of lavendustin A analogues that inhibit EGFR and Syk tyrosine kinases, as well as tubulin polymerization

[Mu; Coffing; Riese II; Geahlen; Verdier-Pinard; Hamel; Johnson; Cushman Journal of Medicinal Chemistry, 2001 , vol. 44, # 3 p. 441 - 452]

Anticonvulsant activity of some 4-aminobenzamides

[Journal of Medicinal Chemistry, , vol. 27, # 6 p. 779 - 782]

Anticonvulsant activity of some 4-aminobenzamides

[Journal of Medicinal Chemistry, , vol. 27, # 6 p. 779 - 782]

Potential central nervous system active agents. 1. Synthesis of aromatic N-benzyl amides

[Agwada, Vincent C. Journal of Chemical & Engineering Data, 1982 , vol. 27, # 4 p. 479 - 481]

Design, synthesis, and biological evaluation of a series of lavendustin A analogues that inhibit EGFR and Syk tyrosine kinases, as well as tubulin polymerization

[Journal of Medicinal Chemistry, , vol. 44, # 3 p. 441 - 452]

More Articles...