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Spebrutinib besylate

This product is for research use only, not for human use. We do not sell to patients.

Spebrutinib besylate
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
500mg$750To Be Confirmed
1g$1250To Be Confirmed
5g$3165To Be Confirmed

Cat #: V4768 CAS #: 1360053-81-1 Purity ≥ 98%

Description: Spebrutinib (formerly known as AVL-292 and CC-292) is a novel, potent, covalent/irreversible, orally bioactive, and highly selective Btk kinase inhibitor with an IC50 of 0.5 nM.

References: Evans EK, et al. Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans. J Pharmacol Exp Ther. 2013 Aug;346(2):219-28.

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Molecular Weight (MW)581.62
Molecular FormulaC28H28FN5O6S
CAS No.1360053-81-1
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
SMILES CodeCOCCOC1=CC=C(NC2=NC=C(F)C(NC3=CC=CC(NC(C=C)=O)=C3)=N2)C=C1.O=S(C4=CC=CC=C4)(O)=O
SynonymsAVL292; AVL-292; AVL 292; CC292; CC-292; CC 292
ProtocolIn VitroSpebrutinib (CC-292) is a covalent, highly selective, orally active inhibitor of Btk with IC50 value of 0.5 nM. Spebrutinib also less potently inhibits Yes, c-Src, Brk, Lyn, and Fyn with IC50s of 723 nM, 1.729 μM, 2.43 μM, 4.4 μM, and 7.15 μM, rspectively. Extensive analysis has revealed that the EC50 of Btk occupancy from a Spebrutinib dose-response in Ramos cells (EC50=6 nM) correlated directly with the cellular EC50 of Btk kinase inhibition with Spebrutinib (EC50=8 nM). Furthermore, the concentration at which Spebrutinib inhibits 90% of Btk activity in Ramos cells is 35 nM while the concentration of Spebrutinib required for 90% occupancy of Btk is 39 nM.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM1.7193 mL8.5967 mL17.1934 mL34.3867 mL
5mM0.3439 mL1.7193 mL3.4387 mL6.8773 mL
10mM0.1719 mL0.8597 mL1.7193 mL3.4387 mL
20mM0.0860 mL0.4298 mL0.8597 mL1.7193 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.