PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 14990704-2 2004 Roscovitine (Rosco) is a purine derivative that inhibits cyclin-dependent kinase 1 (cdk1), cdk2, cdk5, cdk7, and cdk9, which are key regulators of the cell cycle and transcription. purine 25-31 cyclin dependent kinase 1 Homo sapiens 57-82 14990704-2 2004 Roscovitine (Rosco) is a purine derivative that inhibits cyclin-dependent kinase 1 (cdk1), cdk2, cdk5, cdk7, and cdk9, which are key regulators of the cell cycle and transcription. purine 25-31 cyclin dependent kinase 1 Homo sapiens 84-88 25541464-0 2015 Yeast as a model system to screen purine derivatives against human CDK1 and CDK2 kinases. purine 34-40 cyclin dependent kinase 1 Homo sapiens 67-71 11417113-8 2001 It is now reported that CDK1 inhibitory activities of purine analogs correlate with the physiochemical parameters of purine analogs. purine 54-60 cyclin dependent kinase 1 Homo sapiens 24-28 11417113-8 2001 It is now reported that CDK1 inhibitory activities of purine analogs correlate with the physiochemical parameters of purine analogs. purine 117-123 cyclin dependent kinase 1 Homo sapiens 24-28 10683156-7 2000 Addition of deoxyribonucleosides shows that rapid S-phase condensation is suppressed by a novel checkpoint mechanism: purine (but not pyrimidine) deoxyribonucleosides, like reverse transformation, suppress cyclin B/p34(cdc2) activation by caffeine, but not cyclin B accumulation. purine 118-124 cyclin dependent kinase 1 Homo sapiens 219-223 9553063-13 1998 SBCRK and histidine-tagged CRK3 activities were inhibited by the purine analogue olomoucine with an IC50 of 28 and 42 microM, respectively, 5-6-fold higher than human p34(cdc2)/cyclinB. purine 65-71 cyclin dependent kinase 1 Homo sapiens 171-175 26207228-2 2015 It is a broad-range purine inhibitor, which inhibits CDK1, CDK2, CDK5 and CDK7, but is a poor inhibitor for CDK4 and CDK6. purine 20-26 cyclin dependent kinase 1 Homo sapiens 53-57 12392733-1 2002 Based on our previous experiences with synthesis of purines, novel 2,6,9-trisubstituted purine derivatives were prepared and assayed for the ability to inhibit CDK1/cyclin B kinase. purine 52-58 cyclin dependent kinase 1 Homo sapiens 160-164 25541464-4 2015 In the present study, taking advantage of the fact that deletion of the yeast CDC28 gene is functionally complemented by human CDK1 or CDK2, we set up an in vivo screen system to evaluate the inhibitory potency of purine derivatives against these two human Cdks. purine 214-220 cyclin dependent kinase 1 Homo sapiens 127-131 15308730-4 2004 In contrast, roscovitine and other purine PCIs inhibit with high potency only CDK1, CDK2, CDK5, and CDK7, and they specifically inhibit the expression of viral but not cellular genes. purine 35-41 cyclin dependent kinase 1 Homo sapiens 78-82 24304238-1 2014 Evaluation of the effects of purine C-8 substitution within a series of CDK1/2-selective O(6)-cyclohexylmethylguanine derivatives revealed that potency decreases initially with increasing size of the alkyl substituent. purine 29-35 cyclin dependent kinase 1 Homo sapiens 72-76