Home > Compound List > Product Information
Aurintricarboxylic acid_Molecular_structure_CAS_4431-00-9)
Click picture or here to close

Aurintricarboxylic acid

Catalog No. 123269 Name Sigma Aldrich
CAS Number 4431-00-9 Website http://www.sigmaaldrich.com
M. F. C22H14O9 Telephone 1-800-521-8956
M. W. 422.34116 Fax
Purity Email
Storage Chembase ID: 104121

SYNONYMS

Title
金精三羧酸
IUPAC name
5-[(3-carboxy-4-hydroxyphenyl)(3-carboxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxybenzoic acid
IUPAC Traditional name
aurintricarboxylic acid
Synonyms
ATA

DATABASE IDS

CAS Number 4431-00-9
MDL Number MFCD00011663
EC Number 224-628-1

PROPERTIES

Compostion Dye content, 85%
Empirical Formula (Hill Notation) C22H14O9
Absorption Wavelength λmax 552 nm
Melting Point 300 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
RTECS GU4790000
Safety Statements 26
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Readily polymerizes in aqueous solution, forming a stable free radical that inhibits protein-nucleic acid interactions. It is a potent inhibitor of ribonuclease and topoisomerase II by preventing the binding of the nucleic acid to the enzyme. It stimulates tyrosine phosphorylation processes including the Jak2/STAT5 pathway in NB2 lymphoma cells, ErbB4 in neuroblastoma cells, and MAP kinases, Shc proteins, phosphatidylinositide 3-kinase and phospholipase Cγ in PC12 cells. Inhibits apoptosis. It prevents down-regulation of Ca2+ -impermeable GluR2 receptors and inhibits calpain, a Ca2+ -activated protease that is activated during apoptosis.
Other Notes
May contain a substantial amount of polymeric material
Application
Used extensively as a powerful inhibitor of cellular processes which are dependent on the formation of protein-nucleic acid complexes.1,2
Description (简体中文)
Biochem/physiol Actions
易于在水溶液中聚合,形成可抑制蛋白质-核酸相互作用的稳定自由基。它是核糖核酸酶和拓扑异构酶 II 的强效抑制剂,作用机理是阻止核酸与酶的结合。其可促进酪氨酸磷酸化过程,包括 NB2 淋巴瘤细胞中的 Jak2/STAT5 通路,神经母细胞瘤细胞中的 ErbB4,以及 PC12 细胞中的 MAP 激酶、Shc 蛋白、磷脂酰肌醇 3-激酶和磷脂酶 Cγ。抑制细胞凋亡。它可阻止对 Ca2+ 不通透的 GluR2 受体的下调并抑制钙蛋白酶,这是一种在细胞凋亡过程中被活化的 Ca2+ -激活蛋白酶。
Other Notes
可能含有大量的聚合物质
Application
广泛用作依赖于蛋白质-核酸复合物形成的细胞过程的强效抑制剂。1,2

REFERENCES