Chemical & Pharmaceutical Bulletin 2005-10-01

Synthesis of new dihydropyrazines with DNA strand-breakage activity.

Hiroshi Maruoka, Nobuhiro Kashige, Fumio Miake, Tadatoshi Yamaguchi

Index: Chem. Pharm. Bull. 53(10) , 1359-61, (2005)

Full Text: HTML

Abstract

Treatment of 1,2-cyclohexanedione with 1,2-diamines, e.g. ethylenediamine and cis-(and trans-)1,2-diaminocyclohexane, caused [4+2] cyclocondensation to give the corresponding dihydropyrazine derivatives (compounds 1-6). They exhibited stronger DNA strand-breakage activity than that of dihydropyrazines, which has already been reported in previous papers.


Related Compounds

Related Articles:

Chemical modification of cationic groups in the polypeptide cardiac stimulant anthopleurin-A.

1995-02-01

[Toxicon 33(2) , 187-99, (1995)]

Modification of arginine-198 in sarcoplasmic reticulum Ca2+-ATPase by 1,2-cyclohexanedione causes inhibition of formation of the phosphoenzyme intermediate from inorganic phosphate.

1997-08-22

[J. Biol. Chem. 272(34) , 21142-50, (1997)]

Evidence for an essential arginine in the flavoprotein nitroalkane oxidase.

2001-01-01

[J. Enzym. Inhib. 16(2) , 157-63, (2001)]

Modification of arginine residues in ovine prolactin by 1,2-cyclohexanedione. Effect on binding capacity to lactogenic receptors.

1994-07-01

[Int. J. Pept. Protein Res. 44(1) , 31-5, (1994)]

Identification of arginyl residues located at the ATP binding site of sarcoplasmic reticulum Ca2+-ATPase. Modification with 1,2-cyclohexanedione.

1996-11-15

[J. Biol. Chem. 271(46) , 28933-41, (1996)]

More Articles...