(Q34706737)

4 August 2017

title

Structure-activity relationship study of 2,4-diaminothiazoles as Cdk5/p25 kinase inhibitors (English)

1 reference

4 August 2017

7

Kenneth S Kosik

1 reference

4 August 2017

Joydev K Laha

1

1 reference

4 August 2017

Xuemei Zhang

2

1 reference

4 August 2017

Lixin Qiao

3

1 reference

4 August 2017

Min Liu

4

1 reference

4 August 2017

Snigdha Chatterjee

5

1 reference

4 August 2017

Shaughnessy Robinson

6

1 reference

4 August 2017

Gregory D Cuny

8

1 reference

4 August 2017

language of work or name

English

0 references

publication date

3 February 2011

1 reference

Bioorganic & Medicinal Chemistry Letters

4 August 2017

published in

1 reference

4 August 2017

volume

21

1 reference

4 August 2017

issue

7

1 reference

4 August 2017

page(s)

2098-2101

1 reference

Dinaciclib (SCH 727965), a novel and potent cyclin-dependent kinase inhibitor.

4 August 2017

cites work

1 reference

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Anti-diabetic drugs inhibit obesity-linked phosphorylation of PPARgamma by Cdk5.

7 July 2018

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Optimization of 6,6-dimethyl pyrrolo[3,4-c]pyrazoles: Identification of PHA-793887, a potent CDK inhibitor suitable for intravenous dosing

7 July 2018

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No difference in kinetics of tau or histone phosphorylation by CDK5/p25 versus CDK5/p35 in vitro

7 July 2018

1 reference

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Kinase inhibitors as potential therapeutics for acute and chronic neurodegenerative conditions

7 July 2018

1 reference

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Potent and cellularly active 4-aminoimidazole inhibitors of cyclin-dependent kinase 5/p25 for the treatment of Alzheimer's disease

7 July 2018

1 reference

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Synthesis and biological activities of aminopyrimidyl-indoles structurally related to meridianins.

7 July 2018

1 reference

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Synthesis and cytotoxic activity of new azepino[3',4':4,5]pyrrolo[2,1-a]isoquinolin-12-ones

7 July 2018

1 reference

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Dopaminergic and glutamatergic signaling crosstalk in Huntington's disease neurodegeneration: the role of p25/cyclin-dependent kinase 5.

7 July 2018

1 reference

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Role of the active-site solvent in the thermodynamics of factor Xa ligand binding

7 July 2018

1 reference

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The role of CDK5/P25 formation/inhibition in neurodegeneration

7 July 2018

1 reference

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Mammalian cyclin-dependent kinases

7 July 2018

1 reference

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Recent evidence regarding a role for Cdk5 dysregulation in Alzheimer's disease

7 July 2018

1 reference

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Mechanism of CDK5/p25 binding by CDK inhibitors

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Cyclin-dependent kinase-5 in neurodegeneration.

7 July 2018

1 reference

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GSK-3-selective inhibitors derived from Tyrian purple indirubins

7 July 2018

1 reference

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Semi-synthesis, topoisomerase I and kinases inhibitory properties, and antiproliferative activities of new rebeccamycin derivatives.

7 July 2018

1 reference

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Cyclin-dependent kinase 5 is a mediator of dopaminergic neuron loss in a mouse model of Parkinson's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

A catch-and-release strategy for the combinatorial synthesis of 4-acylamino-1,3-thiazoles as potential CDK5 inhibitors

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Aloisines, a new family of CDK/GSK-3 inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity, and cellular effects

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Pharmacological inhibitors of cyclin-dependent kinases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Structure and regulation of the CDK5-p25(nck5a) complex

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Deregulation of Cdk5 in a mouse model of ALS: toxicity alleviated by perikaryal neurofilament inclusions

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Paullones are potent inhibitors of glycogen synthase kinase-3beta and cyclin-dependent kinase 5/p25.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Hyperphosphorylated tau and neurofilament and cytoskeletal disruptions in mice overexpressing human p25, an activator of cdk5

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Inhibition of cyclin-dependent kinases, GSK-3beta and CK1 by hymenialdisine, a marine sponge constituent

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Conversion of p35 to p25 deregulates Cdk5 activity and promotes neurodegeneration

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

p35 is a neural-specific regulatory subunit of cyclin-dependent kinase 5

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Clubbed thiazoles by MAOS: a novel approach to cyclin-dependent kinase 5/p25 inhibitors as a potential treatment for Alzheimer's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Cdk5 is involved in NFT-like tauopathy induced by transient cerebral ischemia in female rats

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Clausine Z, a new carbazole alkaloid from Clausena excavata with inhibitory activity on CDK5.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Defining Cdk5 ligand chemical space with small molecule inhibitors of tau phosphorylation.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Hyperphosphorylation and aggregation of tau in experimental autoimmune encephalomyelitis

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Discovery and SAR of 2-aminothiazole inhibitors of cyclin-dependent kinase 5/p25 as a potential treatment for Alzheimer's disease

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Effect of stereochemistry on the anti-HIV activity of chiral thiourea compounds

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Development of an assay to screen for inhibitors of tau phosphorylation by cdk5.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Cdk5 is a key factor in tau aggregation and tangle formation in vivo

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Pyrazolo[3,4-b]quinoxalines. A new class of cyclin-dependent kinases inhibitors

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Indirubins inhibit glycogen synthase kinase-3 beta and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors?

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Identification of the 23 kDa subunit of tau protein kinase II as a putative activator of cdk5 in bovine brain

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

A brain-specific activator of cyclin-dependent kinase 5.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3062192

Design and synthesis of quinolin-2(1H)-one derivatives as potent CDK5 inhibitors

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21353545

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Calpain-dependent proteolytic cleavage of the p35 cyclin-dependent kinase 5 activator to p25

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21353545

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Structure-activity relationships of 3,4-dihydro-1H-quinazolin-2-one derivatives as potential CDK5 inhibitors

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21353545

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BMCL.2011.01.140

1 reference

4 August 2017

1 reference

4 August 2017

1 reference