TBCA
CAS No. 934358-00-6
TBCA( Casein Kinase II Inhibitor III, TBCA )
Catalog No. M27483 CAS No. 934358-00-6
TBCA is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
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| 10MG | 133 | Get Quote |
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| 25MG | 217 | Get Quote |
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| 50MG | 320 | Get Quote |
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| 100MG | Get Quote | Get Quote |
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Biological Information
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Product NameTBCA
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NoteResearch use only, not for human use.
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Brief DescriptionTBCA is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases.
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DescriptionTBCA is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases.(In Vitro):TBCA inhibits CK2 double mutant (Val66 Ile174) with an IC50 of 0.68 μM. TBCA (0-100 μM; 24 hours) shows a drastic effect on Jurkat cells viability . TBCA dose-dependently inhibits platelet aggregation and secretion induced by various agonists including CRP, 2-MeSADP, AYPGKF and SFLLRN. TBCA also inhibits phosphorylation of PDK1, Akt, and GSK3β induced by AYPGKF.
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In VitroTBCA (0-100 μM; 24 hours) shows a drastic effect on Jurkat cells viability.TBCA also inhibits CK2 double mutant (Val66 Ile174) with an IC50 of 0.68 μM.TBCA dose-dependently inhibits platelet aggregation and secretion induced by various agonists including 2-MeSADP, AYPGKF, SFLLRN, and CRP. TBCA also inhibits phosphorylation of PDK1, Akt, and GSK3β induced by AYPGKF. Cell Viability Assay Cell Line:Jurkat cells Concentration:0-100 μM Incubation Time:24 hours Result:The viability of Jurkat cells was reduced.
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In Vivo——
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SynonymsCasein Kinase II Inhibitor III, TBCA
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PathwayMetabolic Enzyme/Protease
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TargetCasein Kinase
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number934358-00-6
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Formula Weight463.74
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Molecular FormulaC9H4Br4O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (215.64 mM)
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SMILESC(=C/C(O)=O)\C1=C(Br)C(Br)=C(Br)C(Br)=C1
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Chemical Name——
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.Buerge IJ, et al. Stereoselective Metabolism of the Sterol Biosynthesis Inhibitor Fungicides Fenpropidin, Fenpropimorph, and Spiroxamine in Grapes, Sugar Beets, and Wheat. J Agric Food Chem. 2016 Jul 6;64(26):5301-9.
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