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Merck

A36883

Sigma-Aldrich

金精三羧酸 铵盐

ACS reagent

别名:

ATA, 亚氨基三羧酸铵, 铝试剂

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About This Item

线性分子式:
C22H14O9 · 3NH3
CAS号:
分子量:
473.43
顏色索引編號:
43810
Beilstein:
3900820
EC號碼:
MDL號碼:
分類程式碼代碼:
12171500
PubChem物質ID:
NACRES:
NA.47

生物源

synthetic

品質等級

等級

ACS reagent

形狀

powder or crystals

雜質

≤0.1% insolubles

燃燒殘留物

≤0.2%

顏色

dark red

mp

220-225 °C (dec.) (lit.)

溶解度

water: soluble 100 mg/mL

λmax

450 nm
522 nm (2nd)

應用

diagnostic assay manufacturing
hematology
histology

儲存溫度

room temp

SMILES 字串

N.N.N.OC(=O)c1cc(ccc1O)\C(c2ccc(O)c(c2)C(O)=O)=C3/C=CC(=O)C(=C3)C(O)=O

InChI

1S/C22H14O9.3H3N/c23-16-4-1-10(7-13(16)20(26)27)19(11-2-5-17(24)14(8-11)21(28)29)12-3-6-18(25)15(9-12)22(30)31;;;/h1-9,23-24H,(H,26,27)(H,28,29)(H,30,31);3*1H3

InChI 密鑰

AIPNSHNRCQOTRI-UHFFFAOYSA-N

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應用

铝试剂

生化/生理作用

金精三羧酸易于在水溶液中聚合,形成稳定的自由基,抑制蛋白质-核酸相互作用。它通过阻止核酸与酶的结合而成为核糖核酸酶和拓扑异构酶 II 的有效抑制剂。它刺激酪氨酸磷酸化过程,包括 NB2 淋巴瘤细胞中的 Jak2/STAT5 途径,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 C。金精三羧酸抑制许多细胞类型的细胞凋亡。其神经保护作用,可能是由于其能够阻止 Ca2+ 不可渗透的 GluR2 受体的下调或其抑制钙蛋白酶的能力,钙蛋白酶是一种在凋亡过程中被激活的 Ca2+ 激活的蛋白酶。

其他說明

可能含有大量的聚合物材料。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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Jakyung Yoo et al.
Advances in protein chemistry and structural biology, 87, 219-247 (2012-05-23)
DNA methyltransferases (DNMTs) are promising epigenetic targets for the development of novel anticancer drugs and other diseases. Molecular modeling and experimental approaches are being used to identify and develop inhibitors of human DNMTs. Most of the computational efforts conducted so
Moonhee Lee et al.
Neurobiology of aging, 34(5), 1451-1461 (2012-11-28)
Aberrant complement activation is known to exacerbate the pathology in a spectrum of degenerative diseases of aging. We previously reported that aurin tricarboxylic acid (ATA) is an orally effective agent which prevents formation of the membrane attack complex of complement.
Hui-Chen Hung et al.
The Journal of antimicrobial chemotherapy, 65(4), 676-683 (2010-01-22)
Enterovirus 71 (EV71) causes serious diseases in humans. The aim of this study was to examine the effects of aurintricarboxylic acid (ATA) on EV71 replication and to explore the underlying mechanism. To measure the activity of ATA in inhibiting the
Hui-Chen Hung et al.
Antiviral research, 81(2), 123-131 (2008-11-19)
There is a continuing threat that the highly pathogenic avian influenza virus will cause future influenza pandemics. In this study, we screened a library of compounds that are biologically active and structurally diverse for inhibitory activity against influenza neuraminidase (NA).
Jakyung Yoo et al.
Journal of molecular modeling, 18(4), 1583-1589 (2011-08-02)
DNA methyltransferase 1 (DNMT1) is an emerging target for the treatment of cancer, brain disorders, and other diseases. Currently, there are only a few DNMT1 inhibitors with potential application as therapeutic agents or research tools. 5,5-Methylenedisalicylic acid is a novel

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