Vecabrutinib
CAS No. 1510829-06-7
Vecabrutinib( SNS 062 | SNS062 | SNS-062 )
Catalog No. M12111 CAS No. 1510829-06-7
Vecabrutinib (SNS-062) is a potent, reversible, non-covalent BTK inhibitor with IC50 of 2.9 and 4.4 nM for WT BTK and C481S BTK, respectively;
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 219 | In Stock |
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| 5MG | 186 | In Stock |
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| 10MG | 306 | In Stock |
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| 25MG | 497 | In Stock |
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| 50MG | 644 | In Stock |
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| 100MG | 904 | 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 NameVecabrutinib
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NoteResearch use only, not for human use.
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Brief DescriptionVecabrutinib (SNS-062) is a potent, reversible, non-covalent BTK inhibitor with IC50 of 2.9 and 4.4 nM for WT BTK and C481S BTK, respectively;
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DescriptionVecabrutinib (SNS-062) is a potent, reversible, non-covalent BTK inhibitor with IC50 of 2.9 and 4.4 nM for WT BTK and C481S BTK, respectively;Binds to Tec kinase family members BTK (Kd=0.3 nM) and ITK (Kd=2.2 nM), but not bind EGFR, active in vitro in cells with the C481S mutation;Inhibits pBTK in human whole blood with IC50 of 50 nM, demonstrates favorable pharmacokinetic properties, shows potential for overcoming the ibrutinib resistance due to C481S mutantion in BTK.Blood Cancer Phase 2 Clinical.
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In VitroVecabrutinib inhibits pBTK in human whole blood with an average IC50 of 50 nM. Vecabrutinib inhibits WT and C481S BTK with similar IC50s (pBTK IC50s: WT BTK 2.9 nM, C481S BTK 4.4 nM). In a recombinant kinase assay, IC50s of Vecabrutinib against WT BTK and C481S BTK are 4.6 nM and 1.1 nM. Vecabrutinib retains activity against the mutated BTK variant. Vecabrutinib is six times more potent than PCI-32765 and greater than 640 times more potent than acalabrutinib against C481S BTK. Vecabrutinib demonstrates dose-dependent inhibition of BTK in primary patient CLL cells comparable to PCI-32765 via immunoblot for BTK phosphorylation. Vecabrutinib decreases viability of primary CLL cells in the presence of HS5 stromal protection by 5.5%.
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In VivoVecabrutinib has good oral bioavailability in rat and dog (%F ≥ 40%) and a terminal half-life of 5 to 6 hours. Vecabrutinib is well tolerated with continuous drug levels and at exposures much greater than those achieved for PCI-32765.
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SynonymsSNS 062 | SNS062 | SNS-062
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PathwayTyrosine Kinase
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TargetBTK
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RecptorBTK
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Research AreaCancer
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IndicationBlood cancer
Chemical Information
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CAS Number1510829-06-7
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Formula Weight529.925
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Molecular FormulaC22H24ClF4N7O2
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Purity>98% (HPLC)
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SolubilityDMSO : 125 mg/mL. 235.88 mM
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SMILESO=C1N([C@H]2CN(C3=NC=NC(N)=C3F)CC[C@@H]2C(N)=O)CCC[C@H]1NC4=CC(C(F)(F)F)=CC(Cl)=C4
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Chemical Name(3R,3'R,4'S)-1'-(6-amino-5-fluoropyrimidin-4-yl)-3-[3-chloro-5-(trifluoromethyl)anilino]-2-oxo[1,3'-bipiperidine]-4'-carboxamide
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.?Thompson PA, et al. Expert Opin Investig Drugs. 2017 Nov 15:1-12.
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Atuzabrutinib
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