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Merck

SMB00930

Sigma-Aldrich

5-甲氧基-L-色氨酸

98-102%

别名:

5-甲氧基-L-色氨酸, L -2-氨基-3-(5-甲氧基吲哚基)丙酸

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About This Item

经验公式(希尔记法):
C12H14N2O3
CAS号:
分子量:
234.25
分類程式碼代碼:
12352209
NACRES:
NA.26

品質等級

化驗

98-102%

形狀

solid

光學活性

[α]20/D -30 to -28° in water

顏色

off-white to light yellow

儲存溫度

2-8°C

InChI

1S/C12H14N2O3/c1-17-8-2-3-11-9(5-8)7(6-14-11)4-10(13)12(15)16/h2-3,5-6,10,14H,4,13H2,1H3,(H,15,16)/t10-/m0/s1

InChI 密鑰

KVNPSKDDJARYKK-JTQLQIEISA-N

一般說明

5-甲氧基-L-色氨酸是一种 L-色氨酸代谢物,具有抗炎和抗肿瘤活性。5-甲氧基-L-色氨酸由色氨酸羟化酶(TPH)和羟基吲哚 O-甲基转移酶 (HIOMT)合成。5-甲氧基-L-色氨酸是一种 L-色氨酸代谢物,具有抗炎和抗肿瘤活性。其水平在疾病期间降低, 5-甲氧基色氨酸治疗可改善 CKD 小鼠模型的肾纤维化。5-甲氧基色氨酸似乎可在单侧输尿管梗阻小鼠模型中抑制IκB/NFκB信号传导并增强 Keap1/Nrf2 信号传导。

應用

5-甲氧基-L-色氨酸可用于细胞生物学、生物化学和代谢组学研究。

特點和優勢

  • 可用于代谢组学和生物化学研究
  • 用于多种研究应用的优质化合物

其他說明

如需了解生化试剂系列的更多信息,请填写此表

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 3 Oral

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Hua-Ling Chen et al.
The Journal of biological chemistry, 293(28), 11131-11142 (2018-05-26)
5-Methoxytryptophan (5-MTP) is a tryptophan metabolite with recently discovered anti-inflammatory and tumor-suppressing activities. Its synthesis is catalyzed by a hydroxyindole O-methyltransferase (HIOMT)-like enzyme. However, the exact identity of this HIOMT in human cells remains unclear. Human HIOMT exists in several
Huei-Hsuan Cheng et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(33), 13231-13236 (2012-08-02)
Cyclooxygenase-2 (COX-2) expression is induced by mitogenic and proinflammatory factors. Its overexpression plays a causal role in inflammation and tumorigenesis. COX-2 expression is tightly regulated, but the mechanisms are largely unclear. Here we show the control of COX-2 expression by
Dan-Qian Chen et al.
Nature communications, 10(1), 1476-1476 (2019-04-02)
Early detection and accurate monitoring of chronic kidney disease (CKD) could improve care and retard progression to end-stage renal disease. Here, using untargeted metabolomics in 2155 participants including patients with stage 1-5 CKD and healthy controls, we identify five metabolites

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