MK-5108
CAS No. 1010085-13-8
MK-5108( MK 5108 | VX-689 | VX 689 | MK5108 | VX689 )
Catalog No. M10067 CAS No. 1010085-13-8
MK-5108 (VX-689) is a potent, highly selective Aurora-A kinase inhibitor with IC50 of 0.064 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 72 | In Stock |
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10MG | 125 | In Stock |
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25MG | 215 | In Stock |
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50MG | 335 | In Stock |
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100MG | 500 | In Stock |
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200MG | Get Quote | In Stock |
|
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 NameMK-5108
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NoteResearch use only, not for human use.
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Brief DescriptionMK-5108 (VX-689) is a potent, highly selective Aurora-A kinase inhibitor with IC50 of 0.064 nM.
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DescriptionMK-5108 (VX-689) is a potent, highly selective Aurora-A kinase inhibitor with IC50 of 0.064 nM, displays robust selectivity against Aurora-B (220-fold) and Aurora-C (190-fold) in the biochemical assays; also exhibits high selectivity for Aurora-A over a panel of 233 kinases, only one kinase (TrkA) with <100-fold selectivity; inhibits the growth of multiple human cancer cell lines in vitro and in human cancer xenograft models; MK-5108 significantly enhanced the efficacy of docetaxel without increasing its toxicity.Solid Tumors Phase 1 Clinical.
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In Vitro——
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In Vivo——
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SynonymsMK 5108 | VX-689 | VX 689 | MK5108 | VX689
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PathwayCell Cycle/DNA Damage
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TargetAurora Kinase
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RecptorAuroraA
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Research AreaCancer
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IndicationSolid Tumors
Chemical Information
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CAS Number1010085-13-8
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Formula Weight461.94
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Molecular FormulaC22H21ClFN3O3S
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Purity>98% (HPLC)
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SolubilityDMSO: 6.4 mg/mL (Need Warming)
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SMILESOC(=O)[C@@]1(CC2=CC=CC(NC3=NC=CS3)=N2)CC[C@@H](CC1)OC1=C(F)C(Cl)=CC=C1 |r,c:7,13,16,26,30,32,t:5,11|
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Chemical NameCyclohexanecarboxylic acid, 4-(3-chloro-2-fluorophenoxy)-1-[[6-(2-thiazolylamino)-2-pyridinyl]methyl]-, trans-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Shimomura T, et al. Mol Cancer Ther. 2010 Jan;9(1):157-66.
2. Kretzner L, et al. Cancer Res. 2011 Jun 1;71(11):3912-20.
3. Shan W, et al. Clin Cancer Res. 2012 Jun 15;18(12):3352-65.
4. Chefetz I, et al. Cell Cycle. 2011 Jul 1;10(13):2206-14.
molnova catalog
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