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MW 534.82 Da, Purity >98%. CK2 inhibitor (Ki = 0.25 μM), more selective than DMAT. Unlike DMAT, TMCB displays selectivity over PIM1, HIPK2 and DYRK1a (Ki values are 8.65, 15.25 and 11.90 μM, respectively) and a more favourable selectivity profile over a range of other kinases.

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Images

Chemical Structure - TMCB, Selective CK2 inhibitor (AB120289), expandable thumbnail
  • Immunocytochemistry/ Immunofluorescence - TMCB, Selective CK2 inhibitor (AB120289), expandable thumbnail
  • Functional Studies - TMCB, Selective CK2 inhibitor (AB120289), expandable thumbnail

Publications

Key facts

CAS number

905105-89-7

Purity

> 98%

Form

Solid

Molecular weight

534.82 Da

Molecular formula

C11H9Br4N3O2

PubChem identifier

46943415

Nature

Synthetic

Alternative names

Recommended products

MW 534.82 Da, Purity >98%. CK2 inhibitor (Ki = 0.25 μM), more selective than DMAT. Unlike DMAT, TMCB displays selectivity over PIM1, HIPK2 and DYRK1a (Ki values are 8.65, 15.25 and 11.90 μM, respectively) and a more favourable selectivity profile over a range of other kinases.

Key facts

Purity

> 98%

PubChem identifier

46943415

Solubility

Soluble in DMSO to 25 mM (with heating).

Biochemical name

[4,5,6,7-Tetrabromo-2-(Dimethylamino)-1h-Benzimidazol-1-Yl]acetic Acid

Biological description

CK2 inhibitor (Ki = 0.25 μM), more selective than DMAT. Unlike DMAT, TMCB displays selectivity over PIM1, HIPK2 and DYRK1a (Ki values are 8.65, 15.25 and 11.90 μM, respectively) and a more favourable selectivity profile over a range of other kinases.

Canonical SMILES

CN(C)C1=NC2=C(N1CC(=O)O)C(=C(C(=C2Br)Br)Br)Br

InChI

InChI=1S/C11H9Br4N3O2/c1-17(2)11-16-9-7(14)5(12)6(13)8(15)10(9)18(11)3-4(19)20/h3H2,1-2H3,(H,19,20)

InChIKey

PHAOTASRLQMKBE-UHFFFAOYSA-N

IUPAC name

2-[4,5,6,7-tetrabromo-2-(dimethylamino)benzimidazol-1-yl]acetic acid

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate short-term storage conditions

Ambient

Appropriate long-term storage conditions

Ambient

Storage information

The product can be stored for up to 12 months

Product promise

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3 product images

  • Chemical Structure - TMCB, Selective CK2 inhibitor (ab120289), expandable thumbnail

    Chemical Structure - TMCB, Selective CK2 inhibitor (ab120289)

    2D chemical structure image of ab120289, TMCB, Selective CK2 inhibitor

  • Immunocytochemistry/ Immunofluorescence - TMCB, Selective CK2 inhibitor (ab120289), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - TMCB, Selective CK2 inhibitor (ab120289)

    Anti-cIAP2 antibody ab23423 staining cIAP2 in HeLa cells treated withTMCB (ab120289), by ICC/IF. Decrease in cIAP2 expression correlates with increased concentration of TMCB, as described in literature.
    The cells were incubated at 37°C for 10 minutes in media containing different concentrations of ab120289 (TMCB) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with Anti-cIAP2 antibody ab23423 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 goat anti-rabbit polyclonal antibody (Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

  • Functional Studies - TMCB, Selective CK2 inhibitor (ab120289), expandable thumbnail

    Functional Studies - TMCB, Selective CK2 inhibitor (ab120289)

    HeLa cells were incubated at 37°C for 24h with vehicle control (0 μM) and different concentrations of TMCB (ab120289). Decreased expression of cIAP2 in HeLa cells correlates with an increase TMCB concentration, as described in literature.

    Whole cell lysates were prepared with RIPA buffer (containing protease inhibitors and sodium orthovanadate), 40 μg of each were loaded on the gel and the WB was run under reducing conditions. After transfer the membrane was blocked for an hour using 5% BSA before being incubated with Anti-cIAP2 antibody ab23423 at 2 μg/ml and Anti-Actin antibody - Loading Control ab1801 at 2 μg/ml overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/10000 dilution and visualised using ECL development solution.

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