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生物源
synthetic (organic)
品質等級
化驗
≥95%
形狀
powder
顏色
brown
mp
267 °C (dec.) (lit.)
溶解度
1 M NH4OH: 50 mg/mL, clear to slightly hazy
SMILES 字串
O.OC(=O)C1=CC(=O)C=C(N1)C(O)=O
InChI
1S/C7H5NO5.H2O/c9-3-1-4(6(10)11)8-5(2-3)7(12)13;/h1-2H,(H,8,9)(H,10,11)(H,12,13);1H2
InChI 密鑰
SNGPHFVJWBKEDG-UHFFFAOYSA-N
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應用
白屈氨酸水合物已用于洗脱液,作为高效螯合离子色谱(HPCIC)中的络合添加剂进行铁形态分析。它还用作多金属氧酸盐(POM)基镧系杂化化合物的有机配体。
生化/生理作用
白屈氨酸(CDA)是2,6-吡啶二羧酸(DPA)的羟基化衍生物,是一种三阴离子螯合剂。
其属于最有效的“构象受限的谷氨酸类似物”,是谷氨酸脱羧酶抑制剂。
訊號詞
Warning
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Construction of a dinuclear cluster containing La (?) and 4-hydroxypyridine-2, 6-dicarboxylic acid to modify Keggin-type polyoxometalate
Journal of Molecular Structure null
[Use of the radial hemolysis reaction for titrating antirabies sera].
Voprosy virusologii, 29(3), 360-361 (1984-05-01)
The journal of physical chemistry. B, 110(41), 20655-20663 (2006-10-13)
Multifrequency electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) techniques were used to obtain structural information about the copper(II)-chelidamate complex. Well-resolved nitrogen ENDOR spectra could be recorded from solid solution samples by using selective excitation of spin packets.
Acta crystallographica. Section C, Crystal structure communications, 68(Pt 9), o344-o350 (2012-09-01)
Different tautomeric and zwitterionic forms of chelidamic acid (4-hydroxypyridine-2,6-dicarboxylic acid) are present in the crystal structures of chelidamic acid methanol monosolvate, C(7)H(5)NO(5)·CH(4)O, (Ia), dimethylammonium chelidamate (dimethylammonium 6-carboxy-4-hydroxypyridine-2-carboxylate), C(2)H(8)N(+)·C(7)H(4)NO(5)(-), (Ib), and chelidamic acid dimethyl sulfoxide monosolvate, C(7)H(5)NO(5)·C(2)H(6)OS, (Ic). While the zwitterionic
Anti-cancer drug design, 13(8), 837-855 (1999-05-21)
We have explored the potential antitumour activity of DNA-intercalating free radical generators based on compounds constructed from 9-anilinoacridine and chelidamic acid as an iron (II) binding centre. Here we describe their synthesis, DNA cleaving ability and activity against a panel
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