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148776

Sigma-Aldrich

3-羟基邻氨基苯甲酸

97%, for peptide synthesis

别名:

3-羟基邻氨基苯甲酸

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5 G
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5 G
¥1,741.32

About This Item

线性分子式:
HOC6H3(NH2)CO2H
CAS号:
分子量:
153.14
EC 号:
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22

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产品名称

3-羟基邻氨基苯甲酸, 97%

质量水平

方案

97%

表单

solid

反应适用性

reaction type: solution phase peptide synthesis

mp

240 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

Nc1c(O)cccc1C(O)=O

InChI

1S/C7H7NO3/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3,9H,8H2,(H,10,11)

InChI key

WJXSWCUQABXPFS-UHFFFAOYSA-N

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此商品
65390246557184802
assay

90%

assay

99% (AT)

assay

99%

assay

95%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

100

form

solid

form

solid

form

powder

form

solid

一般描述

3-羟基邻氨基苯甲酸是一种氨基苯甲酸,通常用作各种化学反应的中间体。[1]

应用

<ul>
<li><strong>直接抑制酶以减轻喹啉酸的形成:</strong>用于在色氨酸分解代谢的犬尿氨酸途径中合成 2-氨基-3-羧基粘康酸半醛 (ACMS)(Sanz 等人,2022 年)。</li>
</ul>

象形图

Health hazardExclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

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

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    Guifang Gan et al.
    Cell death discovery, 7(1), 173-173 (2021-07-08)
    Sorafenib is the FDA-approved first-line target drug for HCC patients. However, sorafenib only confers 3-5 months of survival benefit with <30% of HCC patients. Thus, it is necessary to develop a sensitizer for hepatocellular carcinoma (HCC) to sorafenib. Here, we
    NO scavenging by 3-hydroxyanthranilic acid and 3-hydroxykynurenine: N-nitrosation leads via oxadiazoles to o-quinone diazides
    C Backhaus, et al.
    Nitric Oxide, 19, 237-244 (2008)
    Andrea Moglia et al.
    Metabolic engineering, 12(3), 223-232 (2009-11-28)
    Phenolic esters like chlorogenic acid play an important role in therapeutic properties of many plant extracts. We aimed to produce phenolic esters in baker's yeast, by expressing tobacco 4CL and globe artichoke HCT. Indeed yeast produced phenolic esters. However, the
    E R Werner et al.
    Biological chemistry Hoppe-Seyler, 366(1), 99-102 (1985-01-01)
    3-Hydroxyanthranilic acid was identified in lymphocyte cultures during allogeneic stimulation. The metabolite and the synthetic product have identical HPLC retention times, fluorescence spectra, fluorescence intensities as a function of pH value and electrochemical behaviour.
    F A Teulings et al.
    Acta vitaminologica et enzymologica, 29(1-6), 108-112 (1975-01-01)
    In comparison with healthy age- and sex-comparable subjects, a significantly higher concentration of unconjugated 3-hydroxyanthranilic acid was detected in the urine of untreated bladder and kidney carcinoma patients. Because of tryptophan metabolite 3-hydroxyanthranilic acid is suspected to be involved in

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