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Product Name:Aminopurvalanol A CAS:220792-57-4 Purity:>97% Package:1mg, 5mg
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| AMINOPURVALANOL A Basic information |
Product Name: | AMINOPURVALANOL A | Synonyms: | NG-97;AMINOPURVALANOL A;(2R)-2-[[6-[(3-AMINO-5-CHLOROPHENYL)AMINO]-9-(1-METHYLETHYL)-9H-PURIN-2-YL]AMINO]-3-METHYL-1-BUTANOL;AMINOPURVALANOL A (APURV);1-Butanol, 2-[[6-[(3-amino-5-chlorophenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-3-methyl-, (2R)-;(R)-2-((6-((3-Amino-5-chlorophenyl)amino)-9-isopropyl-9H-purin-2-yl)amino)-3-methylbutan-1-ol;inhibit,actin polymerization,Inhibitor,Cyclins,cancer cell differention,G2/M-phase transition,Apoptosis,Aminopurvalanol A,Cyclin dependent kinase,CDK,sperm fertilizing ability | CAS: | 220792-57-4 | MF: | C19H26ClN7O | MW: | 403.91 | EINECS: | | Product Categories: | | Mol File: | 220792-57-4.mol | |
| AMINOPURVALANOL A Chemical Properties |
Boiling point | 639.0±65.0 °C(Predicted) | density | 1.40±0.1 g/cm3(Predicted) | storage temp. | Store at +4°C | solubility | Soluble to 100 mM in DMSO | form | White to brownish solid. | pka | 14.51±0.10(Predicted) | color | Off-white to light yellow |
| AMINOPURVALANOL A Usage And Synthesis |
Uses | Aminopurvalanol A is a reversible and ATP-competitive inhibitor of Cdks. | Definition | ChEBI: Aminopurvalanol is a purvalanol and a member of monochlorobenzenes. It has a role as a protein kinase inhibitor. | Biological Activity | Cell-permeable cyclin-dependent kinase inhibitor. IC 50 values are 0.033, 0.033, 0.028 and 0.020 μ M for cdk1/cyclin B, cdk2/cyclin A, cdk2/cyclin E, and cdk5/p35 respectively. Inhibits ERK1 (IC 50 = 12.0 μ M) and ERK2 (IC 50 = 3.1 μ M) and is 3000-fold selective over a range of other protein kinases (IC 50 > 100 μ M). Arrests cell cycle at G 2 /M boundary (IC 50 = 1.25 μ M), and induces apoptosis at concentrations > 10 μ M. | Enzyme inhibitor | This cell-permeable purvalanol derivative (FW = 403.92 g/mol), also named (2R)-2-[[6-[(3-Amino-5-chlorophenyl)amino]-9-(1-methylethyl)- 9H-purin-2-yl]amino]-3-methyl-1-butanol, targets cdk1/cyclin B (IC50 = 0.033 μM), cdk2/cyclin A (IC50 = 0.033 μM), cdk2/cyclin E (IC50 = 0.028 μM), and cdk5/p35 (IC50 = 0.020 μM). It also inhibits ERK1 (IC50 = 12 μM) and ERK2 (IC50 = 3.1 μM), with 3000-times greater selectivity versus a range of other protein kinases (IC50 > 100 μM). Aminopurvalanol A arrests cell cycle at G2/M boundary (IC50 = 1.25 μM), and induces apoptosis at concentrations > 10 μM. | storage | Store at +4°C |
| AMINOPURVALANOL A Preparation Products And Raw materials |
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