Aziridine compounds and methods of making and using them

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

Reexamination Certificate

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C514S046000, C536S025340, C536S025300, C536S023100, C536S022100, C536S025310, C536S026100, C536S026300, C536S026130, C435S006120, C435S007100, C435S007400, C435S007720, C435S007720, C534S558000, C534S560000, C534S639000

Reexamination Certificate

active

06875750

ABSTRACT:
Aziridine derivatives of formula (I)are disclosed which can be used as cofactor for S-adenosyl-L-methionine-dependent methyltransferases.

REFERENCES:
Djordjevic and Stock, “Crystal structure of the chemotaxis receptor methyltransferase CheR suggests a conserved structural motif for binding S-Adenosylmethionine,”Structure5, 545-558, 1997.
Gong, W. et al. “Structure of Pvull DNA-(cytosine N4) methyltransferase, an example of domain permutation and protein fold assignment,”Nucleic Acids Research25 (14), 2702-2715, 1997.
Kagan and Clarke, “Widespread occurrence of three sequence motifs in diverse S-Adenosylmethionine-dependent methyltransferases suggests a common structure for these enzymes,”Archives of Biochemistry and Biophysics310 (2), 417-427, 1994.
Pignot, M., et al., “Coupling of a Nucleoside with DNA by a Methyltransferase,” Angew. Chem., Int. Ed., vol. 37, No. 20, pp. 2888-2891 (1998).

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