TBBz

Suppliers

Names

[ CAS No. ]:
577779-57-8

[ Name ]:
TBBz

[Synonym ]:
4,5,6,7-Tetrabrom-1H-benzimidazol
4,5,6,7-tetrabromobenzimidazole
2oxy
TBBz

Chemical & Physical Properties

[ Melting Point ]:
330-332ºC

[ Molecular Formula ]:
C7H2Br4N2

[ Molecular Weight ]:
433.72000

[ Exact Mass ]:
429.69500

[ PSA ]:
28.68000

[ LogP ]:
4.61290

MSDS

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H319

[ Precautionary Statements ]:
P301 + P310-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges

[ RIDADR ]:
UN 2811 6.1 / PGIII

Precursor & DownStream

Precursor

  • Benzimidazole

DownStream

Articles

An unbiased evaluation of CK2 inhibitors by chemoproteomics: characterization of inhibitor effects on CK2 and identification of novel inhibitor targets.

Mol. Cell. Proteomics 7(6) , 1077-88, (2008)

Recently protein kinases have emerged as some of the most promising drug targets; and therefore, pharmaceutical strategies have been developed to inhibit kinases in the treatment of a variety of disea...

Casein kinase II contributes to the synergistic effects of BMP7 and BDNF on Smad 1/5/8 phosphorylation in septal neurons under hypoglycemic stress.

J. Neurochem. 109(3) , 733-43, (2009)

The combination of bone morphogenetic protein 7 (BMP7) and neurotrophins (e.g. brain-derived neurotrophic factor, BDNF) protects septal neurons during hypoglycemic stress. We investigated the signalin...

Characterizing the convergence of protein kinase CK2 and caspase-3 reveals isoform-specific phosphorylation of caspase-3 by CK2α': implications for pathological roles of CK2 in promoting cancer cell survival.

Oncotarget 4 , 560-71, (2013)

Protein kinase CK2 has emerged as a promising candidate for the treatment of a number of cancers. This enzyme is comprised of two catalytic subunits (CK2 and/or CK2α') that form complexes with homodim...


More Articles


Related Compounds

  • 3-[2-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetyl]-3-azabicyclo[3.2.1]octane-8-carboxylic acid
  • 3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pent-4-ynoyl]-3-azabicyclo[3.2.1]octane-8-carboxylic acid
  • 3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-3-azabicyclo[3.2.1]octane-8-carboxylic acid
  • 3-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-3-azabicyclo[3.2.1]octane-8-carboxylic acid
  • 3-[3-(benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoyl]-3-azabicyclo[3.2.1]octane-8-carboxylic acid
  • 2-({2-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopentyl]acetamido}oxy)propanoic acid
  • rac-2-({[(2R,3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)oxolan-2-yl]formamido}oxy)propanoic acid
  • 2-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hex-5-enamido]oxy}propanoic acid
  • 2-({2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopentyl]acetamido}oxy)propanoic acid
  • 2-({2-[1-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopropyl]acetamido}oxy)propanoic acid
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