VMY 1-103

VMY 1-103 Suppliers list
Company Name: HANGZHOU CLAP TECHNOLOGY CO.,LTD
Tel: 86-571-88216897,88216896 13588875226
Email: sales@hzclap.com
Products Intro: Product Name:VMY 1-103
CAS:1209002-43-6
Purity:18199% Package:10kg 25kg 200 kilograms per barrel Remarks:good
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
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Products Intro: Product Name:VMY-1-103
CAS:1209002-43-6
Purity:98% HPLC Package:5mg,10mg,50mg,100mg,1g,5g
Company Name: Wuhan Jingkangen Biomedical Technology Co., Ltd  
Tel: 13720134139 13720134139
Email: orders@jknbiochem.com
Products Intro: Product Name:VMY-1-103
CAS:1209002-43-6
Purity:98% Package:500mg;1g
Company Name: Nantong QuanYi Biotechnology Co., Ltd  
Tel: 0513-66337626 18051384581
Email: sales@chemhifuture.com
Products Intro: Product Name:VMY-1-103
CAS:1209002-43-6
Purity:98%+ HPLC Package:10mg,100mg,500mg,1g,2g,5g,10g,More
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:VMY-1-103
CAS:1209002-43-6
Purity:0 Package:100mg/RMB 17500;50mg/RMB 13800;25mg/RMB 10600
VMY 1-103 Basic information
Product Name:VMY 1-103
Synonyms:VMY 1-103;2-chloro-N-[2-[[5-(dimethylamino)naphthalen-1-yl]sulfonylamino]ethyl]-4-[[2-[[(2R)-1-hydroxy-3-methylbutan-2-yl]amino]-9-propan-2-ylpurin-6-yl]amino]benzamide;Benzamide, 2-chloro-N-[2-[[[5-(dimethylamino)-1-naphthalenyl]sulfonyl]amino]ethyl]-4-[[2-[[(1R)-1-(hydroxymethyl)-2-methylpropyl]amino]-9-(1-methylethyl)-9H-purin-6-yl]amino]-;2-chloro-N-{2-[5-(dimethylamino)naphthalene-1-sulfonamido]ethyl}-4-[(2-{[(2R)-1-hydroxy-3-methylbutan-2-yl]amino}-9-(propan-2-yl)-9H-purin-6-yl)amino]benzamide
CAS:1209002-43-6
MF:C34H42ClN9O4S
MW:708.27
EINECS:
Product Categories:
Mol File:1209002-43-6.mol
VMY 1-103 Structure
VMY 1-103 Chemical Properties
density 1.39±0.1 g/cm3(Predicted)
pka10.91±0.50(Predicted)
Safety Information
MSDS Information
VMY 1-103 Usage And Synthesis
DescriptionVMY-1-103 is a potent CDK inhibitor, is also a novel dansylated analog of purvalanol B, was shown to inhibit cell cycle progression and proliferation in prostate and breast cancer cells more effectively than purvalanol B. VMY-1-103 , but not purvalanol B, significantly decreased the proportion of cells in S phase and increased the proportion of cells in G(2)/M. VMY-1-103 increased the sub G(1) fraction of apoptotic cells, induced PARP and caspase-3 cleavage and increased the levels of the Death Receptors DR4 and DR5, Bax and Bad while decreasing the number of viable cells, all supporting apoptosis as a mechanism of cell death. VMY-1-103 possesses unique antiproliferative capabilities and that this compound may form the basis of a new candidate drug to treat medulloblastoma.
VMY 1-103 Preparation Products And Raw materials
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