Ambeed.cn

首页 / / / / Cardamonin/豆蔻明

Cardamonin/豆蔻明 {[allProObj[0].p_purity_real_show]}

货号:A256874 同义名: Cardamomin; Alpinetin chalcone

Cardamonin是一种从草豆蔻(Alpinia katsumadai Hayata)中分离的天然黄酮,作为芳基碳氢化合物受体(AhR)激活剂。Cardamonin通过AhR/Nrf2/NQO1途径抑制NLRP3炎性小体活化,从而缓解炎症性肠病。

Cardamonin/豆蔻明 化学结构 CAS号:18956-16-6
Cardamonin/豆蔻明 化学结构
CAS号:18956-16-6
Cardamonin/豆蔻明 3D分子结构
CAS号:18956-16-6
Cardamonin/豆蔻明 化学结构 CAS号:18956-16-6
Cardamonin/豆蔻明 3D分子结构 CAS号:18956-16-6
规格 价格 会员价 库存 数量
{[ item.pr_size ]}

{[ getRatePriceInt(item.pr_rmb, 1,1) ]}

{[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]}

{[ getRatePriceInt(item.pr_rmb, 1,1) ]}

{[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]}
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} 现货 1周 咨询 - +
购物车0 收藏 询单

Cardamonin/豆蔻明 纯度/质量文件 产品仅供科研

货号:A256874 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

全球学术期刊中引用的产品

Nature, 2025, 645, 793-800. Ambeed. [ A201204 , A444152 , A344107 , A952055 ]
Cell, 2025, 188, (21): 5847-5861.e11. Ambeed. [ A122167 ]
Science, 2025, 387(6729): eadp5637. Ambeed. [ A875019 ]
Sig. Transduct. Target. Ther., 2025, 10, 257. Ambeed. [ A104916 ]
Nat. Nanotechnol., 2025, 20, 1502-1513. Ambeed. [ A243018 , A1216705 , A522597 , A125401 , A1355641 ]
更多 >
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。

Cardamonin/豆蔻明 生物活性

描述 Cardamonin, a chalcone extracted from cardamom spice with anti-inflammatory and anti-tumor activities. Cardamonin decreased viability of NPC(Nasopharyngeal carcinoma ) cells in a concentration-dependent manner. The IC50 values were 16.22 μM(CNE-1), 14.34 μM (CNE-2), 16.50 μM (HONE-1), and 68.12 μM (SUNE-1). Moreover, the expression level of the proapoptotic effector protein Bax and Bid was also markedly increased after treatment with cardamonin(15μM) in CNE-2 cells. In vivo, cardamonin (25 mg/kg once every other day from days 13) enhances chemotherapy efficacy.

Cardamonin/豆蔻明 细胞实验

Cell Line
Concentration Treated Time Description References
MDA-MB-231 cells 20 μM 2, 4, 6 h Cardamonin increased ROS levels in MDA-MB-231 cells J Exp Clin Cancer Res. 2019 Aug 27;38(1):377.
MDA-MB-231 cells 20 μM 6 h Cardamonin decreased glucose uptake in MDA-MB-231 cells J Exp Clin Cancer Res. 2019 Aug 27;38(1):377.
MDA-MB-231 cells 20 μM 3, 6, 12 h Cardamonin enhanced mitochondrial oxidative phosphorylation in MDA-MB-231 cells J Exp Clin Cancer Res. 2019 Aug 27;38(1):377.
RAW 264.7 cells 10, 20, 30 µM 24 h Cardamonin inhibited nitric oxide production in LPS-stimulated RAW 264.7 cells without affecting cell viability. Biomolecules. 2021 Apr 29;11(5):661.
THP-1 cells 20 µM 24 h Conditioned medium from cardamonin-pre-treated THP-1 cells did not increase the proliferation of HCT116 cells. Biomolecules. 2021 Apr 29;11(5):661.
Nf1-silenced murine GBM cells 10 and 20 μM 24 and 48 h To evaluate the effect of Cardamonin on NF-κB phosphorylation, results showed that Cardamonin treatment did not reduce NF-κB phosphorylation J Clin Invest. 2023 Nov 15;133(22):e163802.
THP-1 induced macrophages 10 µM and 20 µM 24 h Cardamonin suppressed M2 polarization of TAMs and downregulated TAM-secreted tumorigenic factors, thereby hindering the pro-tumor function of TAMs on ovarian cancer cells. Mol Ther Oncolytics. 2022 Jun 25;26:175-188.
SKOV3 and A2780 cells 0, 10, 20, 30, 40, 50 µM 24 h Cardamonin inhibited the cell viability of SKOV3 and A2780 cells in a concentration-dependent manner. Mol Ther Oncolytics. 2022 Jun 25;26:175-188.
SUM190 10 μM 4 days Cardamonin inhibited the formation of mammosphere-like structures induced by poly(I:C) and suppressed the nuclear translocation of NF-κB and β-catenin. Cell Death Differ. 2015 Feb;22(2):298-310.
SUM190 10 μM 4 days Cardamonin inhibited the increase in the CD44high/CD24−/low cell subpopulation induced by poly(I:C). Cell Death Differ. 2015 Feb;22(2):298-310.
SUM190 10 μM 4 days Cardamonin inhibited the expression of Oct4, c-Myc, and CD44 induced by poly(I:C). Cell Death Differ. 2015 Feb;22(2):298-310.

Cardamonin/豆蔻明 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
ICR mice Acute pain models Intraperitoneal injection 0.3, 1, 3, 10 mg/kg Single administration To investigate the antinociceptive effects of Cardamonin in acute pain models and its possible mechanisms. The results showed that Cardamonin significantly inhibited acetic acid-induced abdominal writhing and dose-dependently suppressed pain responses induced by PMA and glutamate. Molecules. 2020 Nov 18;25(22):5385
SCID mice SUDHL-4 cell xenograft model Intragastric administration 15 mg/kg Once per day for 30 days To evaluate the in vivo anti-tumor effect of Cardamonin on RRAGC-mutant lymphoma, results showed that Cardamonin significantly inhibited tumor growth in RagCT90N-mutant SUDHL-4 cells. BMC Complement Med Ther. 2023 Sep 26;23(1):336
Nude mice MDA-MB-231 xenograft model Intraperitoneal injection 3 mg/kg Once daily for four weeks Cardamonin significantly inhibited tumor growth in the MDA-MB-231 xenograft model J Exp Clin Cancer Res. 2019 Aug 27;38(1):377.
C57Bl/6 mice DSS-induced colitis model Oral 10 mg/kg, 50 mg/kg Daily for 12 days Cardamonin attenuated DSS-induced colitis and reduced the accumulation of inflammatory cells in the colon. Biomolecules. 2021 Apr 29;11(5):661.
BALB/c nude mice Xenograft model of SKOV3 cells or SKOV3 cells mixed with M2 macrophages Intraperitoneal injection 5 mg/kg and 25 mg/kg Once daily for 15 days Cardamonin significantly inhibited tumor growth and lowered the expression of CD163 and CD206. Mol Ther Oncolytics. 2022 Jun 25;26:175-188.
Mice CCI-induced neuropathic pain model Intraperitoneal injection 10 mg/kg Single administration Cardamonin significantly upregulated 5-HT1A receptor subtype expression in the brainstem and spinal cord, indicating its antineuropathic effect in CCI-induced neuropathic pain mice. Molecules. 2021 Jun 16;26(12):3677
Nude mice SUM190 xenograft model Intraperitoneal injection 30 mg/kg Every other day for 20 days Cardamonin almost completely abolished the increase in CSCs induced by poly(I:C). Cell Death Differ. 2015 Feb;22(2):298-310.

Cardamonin/豆蔻明 参考文献

[1]Wang K, et al. Cardamonin, a natural flavone, alleviates inflammatory bowel disease by the inhibition of NLRP3 inflammasome activation via an AhR/Nrf2/NQO1 pathway. Biochem Pharmacol. 2018 Sep;155:494-509.

Cardamonin/豆蔻明 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.70mL

0.74mL

0.37mL

18.50mL

3.70mL

1.85mL

37.00mL

7.40mL

3.70mL

Cardamonin/豆蔻明 技术信息

CAS号18956-16-6
分子式C16H14O4
分子量 270.28
SMILES Code COC1=CC(O)=CC(O)=C1C(=O)C=CC1=CC=CC=C1
MDL No. MFCD00238554
别名 Cardamomin; Alpinetin chalcone
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

溶解方案

DMSO: 120 mg/mL(443.98 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
方案 一
AmBeed 相关网站 AmBeed.cn AmBeed.com
AmBeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    技术支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    积分商城
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    AmBeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。