Purvalanol B

TargetMol
Product Code: TAR-T7167
Supplier: TargetMol
CodeSizePrice
TAR-T7167-5mg5mg£124.00
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Quantity:
TAR-T7167-1mL1 mL * 10 mM (in DMSO)£130.00
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Quantity:
TAR-T7167-10mg10mg£140.00
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Quantity:
TAR-T7167-25mg25mg£192.00
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Quantity:
TAR-T7167-50mg50mg£252.00
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Quantity:
TAR-T7167-100mg100mg£343.00
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Quantity:
TAR-T7167-200mg200mg£482.00
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Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Purvalanol B is a CDK inhibitor that inhibits Cdk2/cyclin A, Cdk2/cyclin E, Cdk5/p35, and Cdk2/cyclin B (IC50s = 6, 9, 6, and 6 nM, respectively)
CAS:
212844-54-7
Formula:
C20H25ClN6O3
Molecular Weight:
432.91
Pathway:
Cell Cycle/Checkpoint; Microbiology/Virology
Purity:
0.98
SMILES:
CC(C)[C@H](CO)Nc1nc(Nc2ccc(C(O)=O)c(Cl)c2)c2ncn(C(C)C)c2n1
Target:
CDK; Parasite

References

Bullard K M , Broccardo C , Keenan S M . Effects of cyclin-dependent kinase inhibitor Purvalanol B application on protein expression and developmental progression in intra-erythrocytic Plasmodium falciparum parasites[J]. Malaria Journal, 2015, 14(1):147. Meijer L , Knockaert M , Lenormand P , et al. p42/p44 MAPKs are intracellular targets of the CDK inhibitor purvalanol[J]. Oncogene, 2002, 21(42):6413-6424. Jiang L, Yu Y, Li Z, et al.BMS-265246, a Cyclin-Dependent Kinase Inhibitor, Inhibits the Infection of Herpes Simplex Virus Type 1.Viruses.2023, 15(8): 1642.