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重要文件

H1771

Sigma-Aldrich

3-羟基- DL -犬尿氨酸

同義詞:

α,2-二氨基-3-羟基-γ-氧苯丁酸

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About This Item

經驗公式(希爾表示法):
C10H12N2O4
CAS號碼:
分子量::
224.21
MDL號碼:
分類程式碼代碼:
12352204
PubChem物質ID:
NACRES:
NA.32

化驗

≥98% (TLC)

品質等級

形狀

powder

溶解度

1 M HCl: 49.00-51.00 mg/mL, clear to very slightly hazy

儲存溫度

2-8°C

SMILES 字串

NC(CC(=O)c1cccc(O)c1N)C(O)=O

InChI

1S/C10H12N2O4/c11-6(10(15)16)4-8(14)5-2-1-3-7(13)9(5)12/h1-3,6,13H,4,11-12H2,(H,15,16)

InChI 密鑰

VCKPUUFAIGNJHC-UHFFFAOYSA-N

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一般說明

3-羟基-DL-犬尿氨酸是一种色氨酸代谢产物,分子量相应的 224 Da。是存在于眼睛晶状体中的发色团或亲水性黄色化合物。3-羟基-DL-犬尿氨酸是由犬尿氨酸在犬尿氨酸 3-单加氧酶 (KMO) 操作下合成的。在犬尿氨酸酶和犬尿氨酸氨基转移酶的作用下,分别代谢为 3-羟基邻氨基苯甲酸和黄尿酸。

應用

3-羟基-DL-犬尿氨酸已被用于:
  • 作为重组人犬尿氨酸酶检测的底物
  • 作为串联质谱 (MS/MS) 分析的引用标准品
  • 作为定量糖尿病视网膜病变患者血清 3-羟基-DL-犬尿氨酸水平的对照品

生化/生理作用

3-羟基-DL-犬尿氨酸 (3-HKYN) 具有抗氧化功能,可防止大脑皮层脂质过氧化。可能调节突触神经传递。Huntington 病患者血浆中 3-HKYN 水平升高。然而,它在神经退行性疾病中的作用仍不十分清楚。犬尿氨酸代谢与谷氨酸能神经传递相关,3-HKYN 水平与精神分裂症的病理生理学相关。

象形圖

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訊號詞

Warning

危險聲明

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


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分析證明 (COA)

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Susanna Campesan et al.
Current biology : CB, 21(11), 961-966 (2011-06-04)
Neuroactive metabolites of the kynurenine pathway (KP) of tryptophan degradation have been implicated in the pathophysiology of neurodegenerative disorders, including Huntington's disease (HD) [1]. A central hallmark of HD is neurodegeneration caused by a polyglutamine expansion in the huntingtin (htt)
A M Myint et al.
Brain, behavior, and immunity, 25(8), 1576-1581 (2011-05-31)
The association between the pro-inflammatory state of schizophrenia and increased tryptophan degradation into kynurenine has been reported. However, the relationship between metabolites from subdivisions of the kynurenine pathway, kynurenic acid and 3-hydroxykynurenine, remains unknown. The present study tested the relationship
Yuri P Tsentalovich et al.
Investigative ophthalmology & visual science, 52(10), 7687-7696 (2011-08-30)
To compare the photochemical properties of UV filter molecules present in the human lens (kynurenine, KN; 3-hydroxykynurenine, 3OHKN; 3-hydroxykynurenine O-β-D-glucoside, 3OHKG; 4-(2-aminophenyl)-4-oxobutanoic acid, AHA; and glutathionyl-kynurenine, GSH-KN) with the use of the following parameters: excited singlet lifetime τ(S), fluorescence quantum
Ruth Condray et al.
The international journal of neuropsychopharmacology, 14(6), 756-767 (2011-01-29)
One branch of the tryptophan catabolic cascade is the kynurenine pathway, which produces neurotoxic [3-hydroxykynurenine (3-OHKY), quinolinic acid] and neuroinhibitory (kynurenic acid) compounds. Kynurenic acid acts as a competitive antagonist at the glycine site of N-methyl-d-asparate receptors at high concentrations
Sarah S Zaher et al.
Investigative ophthalmology & visual science, 52(5), 2640-2648 (2011-01-08)
IDO (indoleamine 2,3-dioxygenase) modulates the immune response by depletion of the essential amino acid tryptophan, and IDO overexpression has been shown to prolong corneal allograft survival. This study was conducted to examine the effect of kynurenines, the products of tryptophan

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