Purine inhibitors of cyclin dependent kinase 2

Organic compounds -- part of the class 532-570 series – Organic compounds – Nitrogen attached directly or indirectly to the purine ring...

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

544276, 544268, 544269, 544118, A61K 3152, C07D47316, C07D47340, C07D47318

Patent

active

058667024

ABSTRACT:
A 2,6,9-trisubstituted purine composition having the following formula: ##STR1## where X is a amino, oxo, thio, of sulfone moiety, R.sub.1 is a lower alkyl, substituted lower alkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, aryl, substituted aryl, heterocycle, hetaryl, substituted hetaryl, aralkyl, heteroaralkyl, heteroalkyl, alkyl alkenyl, alkyl alkynyl, alkyl cycloalkyl, or alkyl cycloheteroalkyl, each having from 1 to 20 carbon atoms; R.sub.2 is hydrogen, lower alkyl, substituted lower alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heterocycle, hetaryl, substituted hetaryl, aralkyl, heteroaralkyl, heteroalkyl, alkyl alkenyl, alkyl alkynyl, alkyl cycloalkyl, or alkyl cycloheteroalkyl; and R.sub.3 is halogen, hydroxyl, thio, alkoxy, alkylthio, lower alkyl, --NR.sub.4 R.sub.5 or a component having the formula: ##STR2## wherein when R.sub.3 is 2-hydroxyethylamino and R.sub.2 is methyl, R.sub.1 -X is not amino, 3-methyl-2-butenylamino, benzylamino, or m-hydroxybenzyl-amino, when R.sub.3 is 2-hydroxyethylamino and R.sub.2 is isopropyl, R.sub.1 -X is not benzylamino, m-hydroxybenzylamino, or 3-methylbutylamino, when R.sub.3 is 2-hydroxyethylamino and R.sub.2 is 2-hydroxyethyl, R.sub.1 -X is not benzylamino and when R.sub.3 is selected from the group consisting of 2-propanol-2-methylamino and 2-dimethylaminoethylamino and R.sub.2 is methyl, then R.sub.1 -X is not benzylamino.

REFERENCES:
patent: 4028353 (1977-06-01), Liotta, et al.
patent: 4405781 (1983-09-01), Bader et al.
patent: 5498819 (1996-03-01), Kaneko et al.
patent: 5508277 (1996-04-01), Regnier et al.
Glab et al., FEBS Letters 353, pp. 207-211, Olomoucine, an inhibitor of the cdc2/cdk2 kinases activity, blocks plant cells at the G1 to S and G2 to M cell cycle transitions (1994).
Abraham et al., Biol Cell 83, pp. 105-120, Cellular effects of olomoucine, an inhibitor of cyclin-dependent kinases (1995).
Schulze-Gahmen et al., Proteins: Structure, Function, and Genetics 22, pp. 378-391, Multiple Modes of Ligand Recognition: Crystal Structures of Cyclin-Dependent Protein Kinase 2 in Complex with ATP and Two Inhibitors, Olomoucine and Isopentenyladenine (1995).
Vesely et al., Eur. J. Biochem. 224, pp. 771-786, Inhibition of cyclin-dependent kinases by purine analogues (1994).
Norman et al., J. Am. Chem. Soc. 118, pp. 7430-7431, A Structure-Based Library Approach to Kinase Inhibitors (1996).
Breshears, et al. Journal of the American Chemical Society, vol. 81, pp. 3789-3792, The Aminolysis of Certain Chlorosubstituted Purines (1959).
Breshears, J. A. C. S 81, 3789 (1959).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Purine inhibitors of cyclin dependent kinase 2 does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Purine inhibitors of cyclin dependent kinase 2, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Purine inhibitors of cyclin dependent kinase 2 will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-1118623

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.