CDK2 INHIBITOR II

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Products Intro: Product Name:SC 221409
CAS:222035-13-4
Purity:>=97% Package:$76.9/1mg;$280.9/5mg;Bulk package Remarks:97%
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Products Intro: Product Name:compound 3
CAS:222035-13-4
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Products Intro: Product Name:CDK2 inhibitor II
CAS:222035-13-4
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Products Intro: Product Name:Cdk2 Inhibitor II
CAS:222035-13-4
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Products Intro: Product Name:CDK2 Inhibitor II
CAS:222035-13-4
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CDK2 INHIBITOR II Basic information
Product Name:CDK2 INHIBITOR II
Synonyms:CDK2 INHIBITOR II;COMPOUND 3;SC 221409;Benzenesulfonamide, 4-[2-(5-bromo-1,2-dihydro-2-oxo-3H-indol-3-ylidene)hydrazinyl]-;CDK2-IN-3 (compound 3);4-(2-(5-Bromo-2-oxoindolin-3-ylidene)hydrazinyl)benzenesulfonamide;4-[2-(5-bromo-1,2-dihydro-2-oxo-3H-indol-3-ylidene)hydrazinyl]-benzenesulfonamide;SC 221409, Cdk2 inhibitor
CAS:222035-13-4
MF:C14H11BrN4O3S
MW:395.23
EINECS:
Product Categories:Aromatics, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals
Mol File:222035-13-4.mol
CDK2 INHIBITOR II Structure
CDK2 INHIBITOR II Chemical Properties
Melting point >272°C (dec.)
density 1.85±0.1 g/cm3(Predicted)
storage temp. Amber Vial, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly, Heated)
form Solid
pka8.81±0.20(Predicted)
color Light Orange to Orange
InChIInChI=1S/C14H11BrN4O3S/c15-8-1-6-12-11(7-8)13(14(20)17-12)19-18-9-2-4-10(5-3-9)23(16,21)22/h1-7,18H,(H2,16,21,22)(H,17,19,20)
InChIKeyODZNNZYRBRRREX-UHFFFAOYSA-N
SMILESC1(S(N)(=O)=O)=CC=C(NN=C2C3=C(NC2=O)C=CC(Br)=C3)C=C1
Safety Information
MSDS Information
CDK2 INHIBITOR II Usage And Synthesis
DescriptionThe cyclin-dependent kinase 2 (Cdk2) works with cyclins A or E to regulate S phase and G2-M transition during the cell cycle. Cdk2 Inhibitor II is a 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC50 = 60 nM). It is cell permeable, reversible, and ATP-competitive.
UsesCDK2 inhibitor II, is a potent, cell-permeable, ATP-competitive, and selective inhibitor of Cdk2.
in vivo

CDK2-IN-3 (2.5-250 μg, topical application, once daily, for 1 week) significantly reduces the incidence of alopecia in neonatal rat model induced by the combination of cyclophosphamide (HY-17420) and doxorubicin (HY-15142A)[1].

Animal Model:Cyclophosphamide (HY-17420)-Doxorubicin (HY-15142A) combination chemotherapy-induced alopecia neonatal Sprague-Dawley rat model (13 days)
Dosage:2.5-250 μg
Administration:Topical application, once daily for 1 week
Result:Effectively prevented alopecia in 50% of rats and provided partial protection in an additional 20%.
IC 50CDK2: 60 nM (IC50)
References[1] FUNK J. Cell Cycle Checkpoint Genes and Cancer[C]. 2006: 0. DOI: 10.1038/npg.els.0006046
[2] STEPHEN T. DAVIS, JR. Prevention of Chemotherapy-Induced Alopecia in Rats by CDK Inhibitors[J]. Science, 2001, 291 5501. DOI: 10.1126/science.291.5501.134
CDK2 INHIBITOR II Preparation Products And Raw materials
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