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Merck
CN

G5254

Sigma-Aldrich

2,5-二羟基苯甲酸

powder

别名:

2,5-DHBA, DHB, 氢醌羧酸, 龙胆酸

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关于此项目

线性分子式:
(HO)2C6H3CO2H
化学文摘社编号:
分子量:
154.12
Beilstein:
2209119
EC 号:
MDL编号:
UNSPSC代码:
12352103
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表单

powder

分子量

154.1
average mol wt 154.12224 Da

颜色

white

mp

204-208 °C (lit.)

溶解性

H2O: soluble
methanol: water: soluble
polar organic solvents: soluble

SMILES字符串

OC(=O)c1cc(O)ccc1O

InChI

1S/C7H6O4/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,8-9H,(H,10,11)

InChI key

WXTMDXOMEHJXQO-UHFFFAOYSA-N

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应用

用作 MALDI-TOF 质谱的基质。肽、蛋白质和糖类离子化的良好基质。适合于反射式质谱。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Strupat K., et al.,
International Journal of Mass Spectrometry and Ion Processes, 111, 89-102 (1991)
Cui Li et al.
European journal of medicinal chemistry, 46(9), 4212-4218 (2011-07-13)
With an aim of developing novel protein tyrosine phosphatase (PTP) 1B inhibitors based on sugar scaffolds, a focused library of benzyl 6-triazolo(hydroxy)benzoic glucosides was efficiently constructed via the modular and selective Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddtion (click chemistry). These glycoconjugates bearing
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly
Wendy R Russell et al.
Bioorganic & medicinal chemistry, 16(8), 4589-4593 (2008-03-04)
Elevated levels of phospholipases, prostaglandin synthases and lipoxygenases in colonic cells at various stages of malignancy indicate a strong link between dietary lipids and colon cancer. Lipoxygenase-catalysed arachidonic acid metabolism plays a key role in colorectal carcinogenesis and has the
Jennifer A Jacobsen et al.
Journal of medicinal chemistry, 54(2), 591-602 (2010-12-30)
Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced hit rates ranging from 29% to 43% for five matrix metalloproteases

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