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Indole-3-carbinol/3-吲哚甲醇 {[allProObj[0].p_purity_real_show]}

货号:A135866 同义名: 吲哚-3-甲醇 / I3C; 3-Indolemethanol

Indole-3-carbinol是一种天然植物激素,主要来源于十字花科蔬菜。它能够抑制 NF-κB 和 IκBα 激酶,具有抑癌作用,但可能在后期促进肿瘤发生。

Indole-3-carbinol/3-吲哚甲醇 化学结构 CAS号:700-06-1
Indole-3-carbinol/3-吲哚甲醇 化学结构
CAS号:700-06-1
Indole-3-carbinol/3-吲哚甲醇 3D分子结构
CAS号:700-06-1
Indole-3-carbinol/3-吲哚甲醇 化学结构 CAS号:700-06-1
Indole-3-carbinol/3-吲哚甲醇 3D分子结构 CAS号:700-06-1
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Indole-3-carbinol/3-吲哚甲醇 纯度/质量文件 产品仅供科研

货号:A135866 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 AhR 其他靶点 纯度
StemRegenin 1 ++

Aryl hydrocarbon receptor (AhR), IC50: 127 nM

99%+
CH-223191 +++

AhR, IC50: 30 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 NF-κB 其他靶点 纯度
Ammonium pyrrolidine-1-carbodithioate 98%
QNZ ++++

NF-κB, IC50: 11 nM

99%+
Sodium 4-Aminosalicylate Dihydrate 98%
Sodium Salicylate 95%
Parthenolide p53 97% HPLC
JSH-23 +

NF-κB, IC50: 7.1 μM

98%
Phenethyl caffeate 98%
Andrographolide 98+%
Curcumin HDAC,Nrf2 98%
SC75741 +++

NF-κB, EC50: 200 nM

99%+
CBL0137 HCl ++

NF-κB, EC50: 0.47 μM

p53 99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Indole-3-carbinol/3-吲哚甲醇 生物活性

描述 Indole-3-carbinol (I3C) inhibits NF-κB activity and also is an Aryl hydrocarbon receptor (AhR) agonist, and an inhibitor of WWP1 (WW domain-containing ubiquitin E3 ligase 1). I3C inhibits the proliferation of THP-1 cells in a dose- and time-dependent manner with minimal toxicity over normal monocytes. I3C could exert its antileukemic effects through AhR activation which is associated with programed cell death and G1 cell cycle arrest in a dose- and time-dependent manner[3]. Treatment with I3C led to repressed colonic inflammation and prevention of microbial dysbiosis caused by colitis, increasing a subset of gram-positive bacteria known to produce butyrate. I3C attenuates colitis primarily through induction of IL-22, which leads to modulation of gut microbiota that promote antiinflammatory butyrate[4]. I3C prevented EtOH (ethanol) -induced liver injury via attenuating the damaging effect of ethanol on the gut-liver-adipose tissue axis[5]. I3C may induce apoptosis in human osteosarcoma MG-63 and U2OS cells via the activation of apoptotic signaling pathways by FOXO3[6].

Indole-3-carbinol/3-吲哚甲醇 细胞实验

Cell Line
Concentration Treated Time Description References
Cutibacterium acnes 0.1 mM 6 days significantly inhibited biofilm formation by C. acnes without affecting planktonic cell growth Microbiol Spectr. 2022 Feb 23;10(1):e0205621.
Cutibacterium acnes 0.1 mM 6 days Significantly inhibited biofilm formation by C. acnes without affecting planktonic cell growth Microbiol Spectr. 2022 Feb 23;10(1):e0205621.
Jurkat cells 10, 50 µM 48 h I3C pretreatment significantly increased PMA/ionomycin-induced IL-2, IL-8, and TNF-α production and enhanced inflammatory responses through activation of NF-κB and NFAT1 signaling pathways. Int J Mol Sci. 2017 Jul 1;18(7):1409.

Indole-3-carbinol/3-吲哚甲醇 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Mice Clostridium difficile infection model Dietary supplementation 1000 ppm Two weeks To investigate the impact of I3C on CDI, results showed that I3C significantly improved survival, reduced weight loss, and disease scores in mice. Ann Surg. 2017 Jun;265(6):1183-1191
Mice Hi-Myc mouse model Intraperitoneal injection 20 mg/kg Three times per week for one month Investigated the therapeutic effects of I3C on prostate tumors in Hi-Myc mice, showing that I3C inhibited tumor growth and AKT activation. Science. 2019 May 17;364(6441):eaau0159

Indole-3-carbinol/3-吲哚甲醇 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT00910884 - Not yet recruiting February 2020 United States, Washington ... 展开 >> Brabant Research, Incorporated Not yet recruiting Spokane Valley, Washington, United States, 99216 Contact: Richard E. Lasker, PhD    509-340-9902    rel@brabantresearch.com 收起 <<
NCT02483624 SLE Phase 1 Terminated - -
NCT02525159 Breast Cancer Phase 3 Completed - -

Indole-3-carbinol/3-吲哚甲醇 参考文献

[1]Mohammadi S, Seyedhosseini FS, et al. Indole-3-carbinol induces G1 cell cycle arrest and apoptosis through aryl hydrocarbon receptor in THP-1 monocytic cell line. J Recept Signal Transduct Res. 2017 Oct;37(5):506-514.

[2]Ampofo E, Lachnitt N, et al. Indole-3-carbinol is a potent inhibitor of ischemia-reperfusion-induced inflammation. J Surg Res. 2017 Jul;215:34-46.

[3]Mohammadi S, Seyedhosseini FS, Behnampour N, Yazdani Y. Indole-3-carbinol induces G1 cell cycle arrest and apoptosis through aryl hydrocarbon receptor in THP-1 monocytic cell line. J Recept Signal Transduct Res. 2017 Oct;37(5):506-514

[4]Busbee PB, Menzel L, Alrafas HR, Dopkins N, Becker W, Miranda K, Tang C, Chatterjee S, Singh U, Nagarkatti M, Nagarkatti PS. Indole-3-carbinol prevents colitis and associated microbial dysbiosis in an IL-22-dependent manner. JCI Insight. 2020 Jan 16;5(1):e127551

[5]Choi Y, Abdelmegeed MA, Song BJ. Preventive effects of indole-3-carbinol against alcohol-induced liver injury in mice via antioxidant, anti-inflammatory, and anti-apoptotic mechanisms: Role of gut-liver-adipose tissue axis. J Nutr Biochem. 2018 May;55:12-25

[6]Lee CM, Lee J, Nam MJ, Park SH. Indole-3-Carbinol Induces Apoptosis in Human Osteosarcoma MG-63 and U2OS Cells. Biomed Res Int. 2018 Nov 29;2018:7970618

Indole-3-carbinol/3-吲哚甲醇 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

6.79mL

1.36mL

0.68mL

33.97mL

6.79mL

3.40mL

67.95mL

13.59mL

6.79mL

Indole-3-carbinol/3-吲哚甲醇 技术信息

CAS号700-06-1
分子式C9H9NO
分子量 147.17
SMILES Code OCC1=CNC2=C1C=CC=C2
MDL No. MFCD00005632
别名 吲哚-3-甲醇 ;I3C; 3-Indolemethanol; NSC 525801; 3-Indolylmethanol; 1H-Indole-3-methanol; Indinol; 3-hydroxymethyl Indole; Indole-3-methanol
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 105 mg/mL(713.44 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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