ChemicalBook--->CAS DataBase List--->749234-11-5

749234-11-5

749234-11-5 Structure

749234-11-5 Structure
IdentificationBack Directory
[Name]

CK2 INHIBITOR II
[CAS]

749234-11-5
[Synonyms]

DMAT >=98% (HPLC)
DMAT(CK2 Inhibitor)
CASEIN KINASE II INHIBITOR;CK2 INHIBITOR
2-Dimethylamino-4,5,6,7-tetrabromobenzimidazole
4,5,6,7-tetrabromo-N,N-dimethyl-1H-benzimidazol-2-amine
1H-Benzimidazol-2-amine, 4,5,6,7-tetrabromo-N,N-dimethyl-
4,5,6,7-tetrabroMo-N,N-diMethyl-1H-benzo[d]iMidazol-2-aMine
[Molecular Formula]

C9H7Br4N3
[MDL Number]

MFCD08705322
[MOL File]

749234-11-5.mol
[Molecular Weight]

476.79
Chemical PropertiesBack Directory
[Melting point ]

>330℃ (Decomposition)
[Boiling point ]

497.7±55.0 °C(Predicted)
[density ]

2.410±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

≥23.85 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
[form ]

solid
[pka]

4.55±0.30(Predicted)
[color ]

White to off-white
[InChI]

1S/C9H7Br4N3/c1-16(2)9-14-7-5(12)3(10)4(11)6(13)8(7)15-9/h1-2H3,(H,14,15)
[InChIKey]

SLPJGDQJLTYWCI-UHFFFAOYSA-N
[SMILES]

CN(C)c1nc2c(Br)c(Br)c(Br)c(Br)c2[nH]1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Description]

DMAT is a cell-permeable inhibitor of casein kinase 2 (CK2; IC50 = 0.13 μM). It also inhibits Pim-1, Pim-3, HIPK2, and HIPK3 (IC50s = 0.15, 0.097, 0.37, and 0.59 μM, respectively). DMAT blocks cell growth and induces cell death in cancer cells, both in culture and in mouse xenografts.
[Uses]

2-Dimethylamino-4,5,6,7-tetrabromobenzimidazole is a novel powerful and selective inhibitor of protein kinase CK2.
[in vivo]

DMAT application in vivo reduces tumor growth in a xenotransplant model by interference with tumor cell proliferation. Biochemical parameters and histology following DMAT administration revealed no alterations in liver tissue[4].

[IC 50]

CK2: 0.13 μM (IC50, Human CK2); PIM1: 0.148 μM (IC50); PIM2: 1.6 μM (IC50); PIM3: 0.097 μM (IC50); HIPK2: 0.37 μM (IC50); HIPK3: 0.59 μM (IC50); DYRK1a: 0.41 μM (IC50); DYRK2: 0.35 μM (IC50); DYRK3: 1.7 μM (IC50); PKD1: 0.18 μM (IC50); CDK2: 0.64 μM (IC50)
[storage]

Store at -20°C
[References]

[1] MARIO A PAGANO. The selectivity of inhibitors of protein kinase CK2: an update.[J]. Biochemical Journal, 2008: 353-365. DOI: 10.1042/bj20080309
[2] HANNA LAWNICKA. Anti-neoplastic effect of protein kinase CK2 inhibitor, 2-dimethylamino-4,5,6,7-tetrabromobenzimidazole (DMAT), on growth and hormonal activity of human adrenocortical carcinoma cell line (H295R) in vitro.[J]. Cell and Tissue Research, 2010, 340 2: 371-379. DOI: 10.1007/s00441-010-0960-1
[3] GABRIELE SASS. Inhibition of experimental HCC growth in mice by use of the kinase inhibitor DMAT.[J]. International journal of oncology, 2011, 39 2: 433-442. DOI: 10.3892/ijo.2011.1037
[4] CHRISTINA WESTMOSE YDE . Induction of cell death in antiestrogen resistant human breast cancer cells by the protein kinase CK2 inhibitor DMAT[J]. Cancer letters, 2007, 256 2: Pages 229-237. DOI: 10.1016/j.canlet.2007.06.010
Spectrum DetailBack Directory
[Spectrum Detail]

CK2 INHIBITOR II(749234-11-5)1HNMR
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