Ambeed.cn

首页 / 抑制剂/激动剂 / 抗感染 / Antibacterial / (+)-(3R,8S)-Falcarindiol

(+)-(3R,8S)-Falcarindiol {[allProObj[0].p_purity_real_show]}

货号:A616303 同义名: 3(R),8(S),9(Z)-Falcarindiol; Falcarindiol

(+)-(3R,8S)-Falcarindiol 是一种从当归(Angelica sinensis)中分离的天然产物,可诱导内质网应激及细胞凋亡,具有免疫抑制作用,适用于自身免疫及过敏性疾病的研究。

(+)-(3R,8S)-Falcarindiol 化学结构 CAS号:225110-25-8
(+)-(3R,8S)-Falcarindiol 化学结构
CAS号:225110-25-8
(+)-(3R,8S)-Falcarindiol 3D分子结构
CAS号:225110-25-8
(+)-(3R,8S)-Falcarindiol 化学结构 CAS号:225110-25-8
(+)-(3R,8S)-Falcarindiol 3D分子结构 CAS号:225110-25-8
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

(+)-(3R,8S)-Falcarindiol 纯度/质量文件 产品仅供科研

货号:A616303 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. Ambeed. [ A122167 ]
Science, 2025, 387(6729): eadp5637. Ambeed. [ A875019 ]
Sig. Transduct. Target. Ther., 2025, 10, 257. Ambeed. [ A104916 ]
Nat. Nanotechnol., 2025. Ambeed. [ A243018 , A1216705 , A522597 , A125401 , A1355641 ]
更多 >

(+)-(3R,8S)-Falcarindiol 生物活性

靶点
  • JNK

描述 (+)-(3R,8S)-Falcarindiol, a natural product isolated and purified from the roots of Angelica sinensis, is a potential anticancer agent that exerts its activity through inducing ER stress and apoptosis, and induces immunosuppressive effects in vitro and in vivo and might be a therapy for autoimmune or allergic diseases. It has protective effect against CCl(4) toxicity, in part, be explained by anti-lipid peroxidation activity associated with the induction of the GSTs including GSTA4.

(+)-(3R,8S)-Falcarindiol 细胞实验

Cell Line
Concentration Treated Time Description References
J774.1 25-100 µM 24 h FAD reduces LPS-induced pro-inflammatory cytokines. Antioxidants (Basel). 2024 Dec 14;13(12):1533.
Raw264.7 25-100 µM 24 h FAD reduces LPS-induced pro-inflammatory cytokines. Antioxidants (Basel). 2024 Dec 14;13(12):1533.
IEC-6 cells 20 μM 48 h Evaluate the safety of Falcarindiol on normal intestinal cells, results showed no significant inhibition on IEC-6 cells at 20 μM Phytomedicine. 2013 Aug 15;20(11):999-1006.
MCF-7 cells 10 μM 48 h Evaluate the antiproliferative effects of Falcarindiol, results showed antiproliferative effects on MCF-7 cells at 10 μM Phytomedicine. 2013 Aug 15;20(11):999-1006.
SW-480 cells 10 μM 48 h Evaluate the antiproliferative effects of Falcarindiol, results showed significant inhibition of SW-480 cell growth at 10 μM Phytomedicine. 2013 Aug 15;20(11):999-1006.
HCT-116 cells 10 μM 48 h Evaluate the antiproliferative effects of Falcarindiol, results showed almost complete inhibition of HCT-116 cell growth at 10 μM Phytomedicine. 2013 Aug 15;20(11):999-1006.
MCF-7 7.5 µM 24 h FAD induces caspase-3-dependent apoptosis by regulating NOX4 and ER stress signaling pathways. Antioxidants (Basel). 2024 Dec 14;13(12):1533.
MDA-MB-231 7.5 µM 24 h FAD induces caspase-3-dependent apoptosis by regulating NOX4 and ER stress signaling pathways. Antioxidants (Basel). 2024 Dec 14;13(12):1533.
Rat primary astrocytes 50 μM 30 min To investigate the inhibitory effect of falcarindiol on LPS/IFN-γ-induced iNOS expression. Results showed that falcarindiol attenuated the activation of IKK and JAK, leading to the blockade of NF-κB and Stat1 activation, thereby suppressing iNOS expression. Br J Pharmacol. 2005 Jan;144(1):42-51.
FHs 74 Int. cells 1 ng/mL to 20 μg/mL 72 h No hormesis effect was observed, and significant inhibition of proliferation was observed at concentrations of 1 μg/mL and above. J Agric Food Chem. 2009 Sep 23;57(18):8290-6.
Caco-2 cells 1 ng/mL to 20 μg/mL 72 h A hormesis effect was observed, with a 42% increase in cell proliferation at 100 ng/mL. Significant inhibition of proliferation was observed at concentrations of 2.5 μg/mL and above. J Agric Food Chem. 2009 Sep 23;57(18):8290-6.

(+)-(3R,8S)-Falcarindiol 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Athymic nude mice HCT-116-Luc xenograft model Intraperitoneal injection 15 mg/kg Once daily for 4 weeks Evaluate the in vivo antitumor effects of Falcarindiol, results showed significant inhibition of HCT-116 tumor growth at 15 mg/kg Phytomedicine. 2013 Aug 15;20(11):999-1006.
BALB/c nude mice MDA-MB-231 xenograft model Intraperitoneal injection 10 or 20 mg/kg Twice weekly FAD reduces tumor volume in a dose-dependent manner. Antioxidants (Basel). 2024 Dec 14;13(12):1533.

(+)-(3R,8S)-Falcarindiol 参考文献

[1]Yoshida J, Seino H, et al. Inhibition of glycogen synthase kinase-3β by falcarindiol isolated from Japanese Parsley (Oenanthe javanica). J Agric Food Chem. 2013 Aug 7;61(31):7515-21.

[2]Seljasen R, Vogt G, et al. Influence of field attack by carrot psyllid (Trioza apicalis Forster) on sensory quality, antioxidant capacity and content of terpenes, falcarindiol and 6-methoxymellein of carrots (Daucus carota L.). J Agric Food Chem. 2013 Mar 20;61(11):2831-8.

(+)-(3R,8S)-Falcarindiol 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.84mL

0.77mL

0.38mL

19.20mL

3.84mL

1.92mL

38.41mL

7.68mL

3.84mL

(+)-(3R,8S)-Falcarindiol 技术信息

CAS号225110-25-8
分子式C17H24O2
分子量 260.37
SMILES Code C=C[C@@H](O)C#CC#C[C@@H](O)/C=C\CCCCCCC
MDL No. N/A
别名 3(R),8(S),9(Z)-Falcarindiol; Falcarindiol; (3R,8S)-Falcarindiol
运输蓝冰
InChI Key QWCNQXNAFCBLLV-YWALDVPYSA-N
Pubchem ID 5281148
存储条件

In solvent -20°C:3-6个月-80°C:12个月

溶解方案

DMSO: 145 mg/mL(556.9 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
方案 二
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。