吲哚-3-丙酮酸CAS号392-12-1
吲哚-3-丙酮酸CAS号392-12-1
吲哚-3-丙酮酸CAS号392-12-1
吲哚-3-丙酮酸CAS号392-12-1

吲哚-3-丙酮酸

¥460.00
50mg
50mg
北京
索莱宝
2026-04-15
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产品详情
中文名称:吲哚-3-丙酮酸中文别名:吲哚-3-丙酮酸
英文名称:Indole-3-pyruvic AcidCAS:392-12-1
产品分类:小分子化合物纯度:≥95%
产品编号品牌纯度规格库存价格
II1300索莱宝≥95%50mg有现货460.00 元
标准名称:3-吲哚丙酮酸英文名称:Indole-3-pyruvic acid
CAS:392-12-1分子式:C11H9NO3
分子量:203.194062948227颜色与性状:米色粉末
密度:1.2621 (rough estimate)沸点:445.2 ℃ at 760 mmHg
熔点:215 °C (dec.) (lit.)水溶性:
CAS392-12-1
中文名称吲哚-3-丙酮酸
英文名称Indole-3-pyruvic Acid
别名3-(3-吲哚基)-2-氧代丙酸;3-(3-Indoly)-2-oxopropanoic acid
分子式C11H9NO3
分子量203.19
规格50mg
溶解性Soluble in DMSO
纯度≥95%
级别Cell Culture
外观(性状)Off-white to light yellow Solid
储存条件Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
运输条件冷藏运输
ECEINECS 206-874-1
MDLMFCD00005640
SMILESC1=CC=C2C(=C1)C(=CN2)CC(=O)C(=O)O
InChIKeyRSTKLPZEZYGQPY-UHFFFAOYSA-N
InChIInChI=1S/C11H9NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H,14,15)
PubChem CID803
Beilstein Number172966
靶点AhR
通路Immunology & Inflammation
背景说明Indole-3-pyruvic acid是一种 AHR 激动剂, 具有抗氧化活性,可用于炎症、焦虑的相关研究。
生物活性Indole-3-pyruvic acid, a keto analogue of tryptophan, is an orally active AHR agonist. Indole-3-pyruvic acid has antioxidant properties, and can be used in the research of inflammation, anxiety[1][2][3].
In VitroIPA directly promoted the differentiation of type 1 regulatory T cells in vitro.[1]RT-PCR[2]:Cell Line: HaCaT cells;Concentration:5-25 mM;Incubation Time:6 h;Result:Inhibited UVB-stimulated mRNA expression of IL-1β, IL-6, and cyclooxygenase 2 (Cox-2).
In VivoAryl Hydrocarbon Receptor (AHR) agonists are promising immunomodulators that potentially maintain immune tolerance. In this study, we examined the ability of indole-3-pyruvic acid (IPA), a major precursor of microbiota-derived AHR agonists and a proagonist of AHR, to activate AHR. The anti-inflammatory effects of IPA were also evaluated in a mouse model of colitis in comparison with Other aromatic pyruvic acids (phenylpyruvic acid and 4-hydroxyphenylpyruvic acid). Among them, IPA showed the strongest ability to activate AHR in vitro and in vivo, and only IPA improved chronic inflammation in an experimental colitis model. IPA attenuated the expression of genes encoding Th1 cytokines and enhanced IL-10 gene expression in the colon. Oral administration of IPA decreased the frequency of IFN-γ+ IL-10- CD4+ T cells and increased that of IFN-γ- IL-10+ CD4+ T cells in the colon lamina propria in a T cell-mediated colitis model.[1]。Animal Model: BALB/c mice[1];Dosage:Fed in MF chow.0.1% for 5 d;Administration: Oral administration;Result:Up-regulated the expression of Cyp1a1 (a biomarker for AHR activation) in the colon.Animal Model: T cell–mediated colitis model of SCID mice[1];Dosage:Fed in MF chow.0.1% for 5 wk;Administration:Oral administration;Result:Suppressed diarrhea and improved colon inflammation.Down-regulated the expression of Th1 and proinflammatory cytokines and upregulated the expression of IL-10 in the colon.Animal Model: HR-1 Hairless Mice[2];Dosage:100 μM;Administration:Dose at skin;Result:Enhanced the epidermal thickness.Attenuated UVB-induced necrosis observed in upper layer of dermis.
数据来源文献[1]. Reiji Aoki, et al. Indole-3-Pyruvic Acid, an Aryl Hydrocarbon Receptor Activator, Suppresses Experimental Colitis in Mice. J Immunol. 2018 Dec 15;201(12):3683-3693.
[2]. Reiji Aoki, et al. Protective effect of indole-3-pyruvate against ultraviolet b-induced damage to cultured HaCaT keratinocytes and the skin of hairless mice. PLoS One. 2014 May 8;9(5):e96804.
[3]. I P Lapin, et al. Anxiolytic effect of indole-3-pyruvic acid (IPA) in mice. Pharmacol Res. 1993 Sep;28(2):129-34.
单位
1mM-5mg24.6075mL
1mM-1mg4.9215mL
1mM-10mg49.215mL
5mM-1mg0.9843mL
5mM-5mg4.9215mL
5mM-10mg9.843mL
10mM-1mg0.4922mL
10mM-5mg2.4608mL
10mM-10mg4.9215mL
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