Compounds that interact with kinases

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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Details

C514S263230, C514S381000, C514S382000, C544S277000, C548S252000, C548S253000

Reexamination Certificate

active

10526388

ABSTRACT:
A method of inhibiting or effecting the activity of protein kinase activity which comprises contacting a protein kinase with a compound of formula (I) being a derivative of a furanose or pyranose form of a monosaccharide, or a pharmaceutically acceptable salt thereof.

REFERENCES:
patent: 1 106 609 (2001-06-01), None
patent: WO96/40705 (1996-12-01), None
patent: WO99/41266 (1999-08-01), None
patent: WO 01/32653 (2001-05-01), None
Garner et al., Journal of Organic Chemistry, vol. 55(12), pp. 3772-3787 (1990).
Kasnar, “Synthesis of ‘Reversed’ and ‘Double Headed’ Nucleosides,” Nucleosides & Nucleotides, vol. 14, Issue 3-5, pp. 341-344 (1995).
Walcazk et al., “Synthesis of reversed azole nucleosides under the Mitsunobu reaction conditions,” Polish J. of Chemistry 70(7), pp. 867-871 (1996).

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