GW297361

Modify Date: 2024-01-23 10:27:10

GW297361 Structure
GW297361 structure
Common Name GW297361
CAS Number 388627-21-2 Molecular Weight 372.42
Density N/A Boiling Point N/A
Molecular Formula C16H12N4O3S2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of GW297361


GW297361 is an oxindole CDK inhibitor that elicits a Pho85-selective response in cells. GW297361 inhibits yeast Cdk1 and Pho85 with IC50s of 20 nM and 400 nM in vitro, respectively[1].

 Names

Name GW297361

 GW297361 Biological Activity

Description GW297361 is an oxindole CDK inhibitor that elicits a Pho85-selective response in cells. GW297361 inhibits yeast Cdk1 and Pho85 with IC50s of 20 nM and 400 nM in vitro, respectively[1].
Related Catalog
Target

yeast Cdk1:20 nM (IC50)

yeast Pho85:400 nM (IC50)

human CDK2:1.9 nM (IC50)

human CDK9:10 nM (IC50)

human CDK1:30 nM (IC50)

human CDK4:300 nM (IC50)

VEGFR2:120 nM (IC50)

SRC:930 nM (IC50)

In Vitro GW297361 (20 μM; 15 min) 部分抑制细胞内的 Cdk1[1]。 Western Blot Analysis[1] Cell Line: YRP1 cells Concentration: 20 μM Incubation Time: 20 μM Result: An intermediate level of the Orc6 was converted to the faster-migrating isoform (lower:upper = 2:1).
References

[1]. Kung C, et al. Selective kinase inhibition by exploiting differential pathway sensitivity. Chem Biol. 2006 Apr;13(4):399-407.  

 Chemical & Physical Properties

Molecular Formula C16H12N4O3S2
Molecular Weight 372.42
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