Alsteropaullone
CAS No. 237430-03-4
Alsteropaullone( 9-Nitropaullone | NSC 705701 )
Catalog No. M13686 CAS No. 237430-03-4
Alsteropaullone (9-Nitropaullone, NSC 705701) is a derivative of kenpaullone, ATP-competitive inhibitor of CDKs and GSK3β, inhibits Cdk1/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E and Cdk5/p25 with IC50 of 35, 15, 200 and 40 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 192 | In Stock |
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| 10MG | 309 | In Stock |
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| 25MG | 525 | In Stock |
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| 50MG | 752 | In Stock |
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| 100MG | 1035 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameAlsteropaullone
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NoteResearch use only, not for human use.
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Brief DescriptionAlsteropaullone (9-Nitropaullone, NSC 705701) is a derivative of kenpaullone, ATP-competitive inhibitor of CDKs and GSK3β, inhibits Cdk1/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E and Cdk5/p25 with IC50 of 35, 15, 200 and 40 nM.
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DescriptionAlsteropaullone (9-Nitropaullone, NSC 705701) is a derivative of kenpaullone, ATP-competitive inhibitor of CDKs and GSK3β, inhibits Cdk1/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E and Cdk5/p25 with IC50 of 35, 15, 200 and 40 nM; exhibits specific antitumor activity against Group 3 medulloblastomas, causes inhibition of cell cycle-related genes, and down-regulation of MYC; inhibits the cytosolic degradation of β-catenin to alter the canonical Wnt signaling pathway in primary axis patterning, reduces tau phosphorylation.
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In VitroAlsterpaullone (0.3, 1, 3 μM; 8 hours) induces apoptosis in leukemia cell line.Alsterpaullone (5, 10, 15, 20, 25, 30 μM; 48 and 72 hours) inhibits the growth of HeLa cells in dose-and time-dependent manner. Treatment with Alsterpaullone causes a time-dependent inhibition of cell growth too. Alsterpaullone (20?μM) induces cell death depending on caspase activity. Cell Viability Assay Cell Line:HeLa cells Concentration:5, 10, 15, 20, 25, 30 μMIncubation Time:48 and 72 hoursResult:The growth of HeLa cells was inhibited in a dose-dependent manner for 48?h and 72?h ranging from 0 to 30?μM.Apoptosis Analysis Cell Line:Jurkat cell line Concentration:0.3, 1, 3 μM Incubation Time:8 hours Result:Induced dose-dependent apoptosis. 1 μM was sufficient to cause apoptosis, 3 μM demonstrated maximal apoptotic effects.Western Blot Analysis Cell Line:HeLa cells Concentration:2, 4, 6, 12, 24 hours Incubation Time:8 hours Result:The cleavage of PARP started at 4?h, while the activation of caspase-3 occurred at 2?h.
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In VivoAlsterpaullone (30 mg/kg, s.c., daily for 2 weeks) reduces tumor growth and increases survival in medulloblastoma xenografts. Animal Model:5-6 week old athymic nude mice Dosage:30 mg/kg Administration : Subcutaneous injections, daily for 2 weeks Result:Antitumor effect in Group 3 medulloblastomas.
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Synonyms9-Nitropaullone | NSC 705701
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PathwayAngiogenesis
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TargetCDK
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RecptorCDK
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Research Area——
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Indication——
Chemical Information
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CAS Number237430-03-4
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Formula Weight293.3
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Molecular FormulaC16H11N3O3
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C1NC2=CC=CC=C2C(NC3=C4C=C([N+]([O-])=O)C=C3)=C4C1
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Chemical Name7,12-dihydro-9-nitro-indolo[3,2-d][1]benzazepin-6(5H)-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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CDK7 and 9 inhibitor...
A potent, selective transcriptional CDK inhibitor with Ki of 2.3 and 0.38 nM for CDK7 and CDK9, respectively; displays >30-fold selectivity over CDK1/2/4, inhibits VEGFR2 with IC50 of 180 nM in a panel of non-CDK kinases.
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CDK12-IN-2
CDK12-IN-2 is an effective and selective inhibitor of CDK12 with an IC50 of 52 nM, >100 μM, >10 μM and 16 μM for CDK12, CDK2, CDK7, and CDK9. CDK12-IN-2 can be used in studies about the function of CDK12.
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Furanodiene
Furanodiene has anti-inflammatory and antioxidant activities, it is active against gram-positive bacteria and Candida albicans.The in vitro effects of Furanodiene were examined on two human breast cancer cell lines, MCF-7 and MDA-MB-231 cells.
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