BiochemProbe — Life Science Research Reagents

CDK2-IN-73 free base · Synonyms: CDK2-IN-4

CDK2-IN-4 is a potent and selective CDK2 inhibitor.

For research use only. Not for human or veterinary use.

Target CDK
Research area Cancer
Purity >98% Stock Inquire

CDK2-IN-73 structure

CAS No.: 2079895-42-2

Download structure (.mol)

Pack sizes & pricing

Size Price SKU Stock
100 mg USD 485.00 BP-01966-100mg In stock Get quote
250 mg USD 885.00 BP-01966-250mg In stock Get quote
500 mg USD 1,385.00 BP-01966-500mg In stock Get quote
1 g USD 1,985.00 BP-01966-1g In stock Get quote
5 g Inquire BP-01966-5g Inquire Inquire

Need another size or custom synthesis? Request a quote.

Description

CDK2-IN-4 is a potent and selective CDK2 inhibitor with an IC50 of 44 nM for CDK2/cyclin A.

Biological activity

In Vitro CDK2-IN-4 (compound 73) demonstrates appreciable nanomolar potency versus CDK2 in isolated kinase assays, the maximal concentration tested in cellular assays (30 μM) had no or limited effects on the growth of cells.

Identifiers

SMILES
O=S(C1=CC=C(C=C1)NC2=NC3=NC=NC3=C(C4=CC(C5=CC=CC=C5)=CC=C4)N2)(N)=O
InChIKey
FUGRWXRQJGJIER-UHFFFAOYSA-N

Specifications

MW (average)
442.4930
Formula
C23H18N6O2S
CAS No.
2079895-42-2
Physical state
Solid
Color
White to yellow
Shipping
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage
Powder 4°C, sealed storage, away from moisture and light; In solvent -20℃ 1 month;

Solubility

Soluble in DMSO

References

[1]. Coxon CR, et al. Cyclin-Dependent Kinase (CDK) Inhibitors: Structure-Activity Relationships and Insights into the CDK-2 Selectivity of 6-Substituted 2-Arylaminopurines. J Med Chem. 2017 Mar 9;60(5):1746-1767.

Same target

Search CDK

Same research area

Search Cancer