Tetrabenazine; TBZ

Code: 5098920001 D2-231

Biochem/physiol Actions

Reversible: yes

Primary TargetVMAT2

General description

A cell permeable benzoquinolizine based compound that acts ...


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€150.20 EACH
€184.75 inc. VAT

Biochem/physiol Actions

Reversible: yes

Primary TargetVMAT2

General description

A cell permeable benzoquinolizine based compound that acts as a monoamine-depleting agent by blocking the activity vesicular monoamine transporter 2. Promotes late-stage differentiation of Pdx1-positive pancreatic progenitor cells into Neurog3 (Ngn3)-positive endocrine precursors without increasing their proliferation. Increases the number of insulin expressing cells in a dose dependent manner (EC50 = 220 nM) and this effect is significantly enhanced when cells are simultaneously treated with dibutyryl cAMP. Embryonic stem cells treated with TBZ and/or dibutyryl cAMP and then grafted into kidney capsule of AKITA mice reduce hyperglycemia, improve fasting blood glucose levels, and show an increase in plasma C-peptide levels.Please note that the molecular weight for this compound is batch-specific due to variable water content.

A cell permeable benzoquinolizine based compound that acts as a monoamine-depleting agent by blocking the activity vesicular monoamine transporter 2. Promotes late-stage differentiation of Pdx1-positive pancreatic progenitor cells into Neurog3 (Ngn3)-positive endocrine precursors without increasing their proliferation. Increases the number of insulin expressing cells in a dose dependent manner (EC50 = 220 nM) and this effect is significantly enhanced when cells are simultaneously treated with dibutyryl cAMP. Embryonic stem cells treated with TBZ and/or dibutyryl cAMP and then grafted into kidney capsule of AKITA mice reduce hyperglycemia, improve fasting blood glucose levels, and show an increase in plasma C-peptide levels.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Other Notes

Sakano, D., et al. 2014. Nat. Chem. Bio.10,141.r>Jankovic, J., et al. 1997. Neurobiology48,1358.Gertrude, P.Q., et al. 1959. J. Pharm. Exp. Ther.127, 103.

Packaging

Packaged under inert gas

10 mg in Glass bottle

Reconstitution

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Warning

Toxicity: Harmful (C)

assay≥98% (HPLC)
coloroff-white
formpowder
InChI keyMKJIEFSOBYUXJB-UHFFFAOYSA-N
InChI1S/C19H27NO3/c1-12(2)7-14-11-20-6-5-13-8-18(22-3)19(23-4)9-15(13)16(20)10-17(14)21/h8-9,12,14,16H,5-7,10-11H2,1-4H3
manufacturer/tradenameCalbiochem®
Quality Level100
solubilityDMSO: 25 mg/mL
storage conditionprotect from light, OK to freeze
storage temp.2-8°C
Cas Number58-46-8
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