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Didymin/香蜂草苷 {[allProObj[0].p_purity_real_show]}

货号:A527436 同义名: 香风草甙 / Neoponcirin; Isosakuranetin-7-O-rutinoside

Didymin 是一种天然来源的黄酮苷类化合物,具有抗氧化、抗炎和抗肿瘤活性。它可通过下调 N-Myc 表达并上调 RKIP,诱导神经母细胞瘤细胞发生凋亡,对 p53 野生型及耐药突变型细胞均表现出作用,常用于癌症机制及相关信号通路的研究。

Didymin/香蜂草苷 化学结构 CAS号:14259-47-3
Didymin/香蜂草苷 化学结构
CAS号:14259-47-3
Didymin/香蜂草苷 3D分子结构
CAS号:14259-47-3
Didymin/香蜂草苷 化学结构 CAS号:14259-47-3
Didymin/香蜂草苷 3D分子结构 CAS号:14259-47-3
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Didymin/香蜂草苷 纯度/质量文件 产品仅供科研

货号:A527436 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Adrenergic Receptor α-adrenergic receptor β-adrenergic receptor 其他靶点 纯度
Ivabradine HCl 98%
Maprotiline HCl 98%
Cisatracurium besylate 96%
Yohimbine HCI 99+%
BMY 7378 ++

α1D-adrenoceptor, pKi: 5.1

α2C-adrenoceptor, pKi: 6.54

+

β1-adrenoceptor, pIC50: 5.1

97%
Asenapine maleate ++++

α2A-adrenergic receptor, pKi: 8.9

α2B-adrenergic receptor, pKi: 8.9

97%
Piribedil ++

adrenoceptor α2A, pKi: 7.1

adrenoceptor α2C, pKi: 7.2

98%
Prazosin HCl 95%
Silodosin 98%
Phenoxybenzamine HCl 98%
Labetalol HCl 98+%
Naftopidil +++

α1D-adrenergic receptor, Ki: 20 nM

α1A-adrenergic receptor, Ki: 3.7 nM

98%
Naftopidil 2HCl +

α1-adrenergic receptor, IC50: 0.2 μM

99%
Alfuzosin HCl 98%
Terazosin HCl 99%
Atipamezole 95%
Phentolamine methanesulfonate salt 99%
Carvedilol 99%
Doxazosin mesylate 99%
Tolazoline HCl 98%
Esmolol HCl 95%
Propranolol HCl ++

β-adrenergic receptor, IC50: 12 nM

99%
Zenidolol HCl ++++

β2-adrenergic receptor, Ki: 0.7nM

β1-adrenergic receptor, Ki: 611nM

98%
Acebutolol HCl 97+%
Carteolol HCl 98+%
Betaxolol 99%
Betaxolol HCl +

β1-adrenergic receptor, IC50: 6 μM

97%
Bisoprolol 97%
Sotalol HCl 95+%
Nebivolol HCl +++

β1-adrenoceptor, IC50: 0.8 nM

99%
Metoprolol 98+%
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。

Didymin/香蜂草苷 生物活性

描述 Didymin, a natural product isolated and purified from the herbs of Clinopodium chinense with antioxidant property, may be a potential therapeutic molecule for the treatment of neurodegenerative disorders associated with oxidative stress.

Didymin/香蜂草苷 细胞实验

Cell Line
Concentration Treated Time Description References
Human umbilical vein endothelial cells (HUVECs) 20 μM 24 h Pre-incubation with didymin prevented the release of various inflammatory cytokines and chemokines in HG-treated HUVECs. Biochem Pharmacol. 2018 Jun;152:1-10
Human umbilical vein endothelial cells (HUVECs) 20 μM 6 h Pre-incubation with didymin prevented HG-induced monocyte adhesion to endothelial cells and inhibited expressions of ICAM-1 and VCAM-1 and activation of NF-κB. Biochem Pharmacol. 2018 Jun;152:1-10
Human umbilical vein endothelial cells (HUVECs) 20 μM 3 h Pre-incubation with didymin prevented HG-induced generation of reactive oxygen species (ROS) and malondialdehyde (MDA). Biochem Pharmacol. 2018 Jun;152:1-10
Human umbilical vein endothelial cells (HUVECs) 10 μM and 20 μM 24 h Pre-incubation with didymin prevented high glucose (HG)-induced loss of cell viability. Biochem Pharmacol. 2018 Jun;152:1-10
H9c2 cardiomyocytes 5, 10, 20 μg/mL 4 h Did pretreatment significantly maintained cell viability and reduced LDH release, alleviating DOX-induced cell injury Chin Herb Med. 2021 Jul 15;14(1):70-78
INS-1 cells 50 µM 24 h To evaluate the effect of Didymin on insulin secretion function in INS-1 cells. Results showed that Didymin improved insulin secretion under high glucose stimulation, reduced excessive insulin secretion under low glucose stimulation, and increased intracellular insulin storage. Diabetol Metab Syndr. 2024 Jan 3;16(1):7
AML12 cells 50 μM 24 h To evaluate the effect of Didymin on PA-induced lipid deposition in AML12 cells. Results showed that Didymin significantly reduced PA-induced lipid accumulation. J Transl Med. 2023 Dec 19;21(1):921
MCF-7/ADR cells 10μM-200μM 48 h Evaluate the chemosensitization effect of Didymin and its inclusion complexes on drug-resistant tumor cells. Results showed that Didymin significantly increased intracellular accumulation of DOX in resistant cells and enhanced the cytotoxicity of DOX. Drug Deliv. 2020 Dec;27(1):54-65
PC12 cells 10μM-200μM 48 h Evaluate the toxicity of Didymin and its inclusion complexes on healthy cell lines. Results showed that cell viability remained above 90% at all tested concentrations, indicating low toxicity of Didymin and its inclusion complexes to healthy cells. Drug Deliv. 2020 Dec;27(1):54-65
H9C2 cells 10μM-200μM 48 h Evaluate the toxicity of Didymin and its inclusion complexes on healthy cell lines. Results showed that cell viability remained above 90% at all tested concentrations, indicating low toxicity of Didymin and its inclusion complexes to healthy cells. Drug Deliv. 2020 Dec;27(1):54-65
HUVEC cells 10μM-200μM 48 h Evaluate the toxicity of Didymin and its inclusion complexes on healthy cell lines. Results showed that cell viability remained above 90% at all tested concentrations, indicating low toxicity of Didymin and its inclusion complexes to healthy cells. Drug Deliv. 2020 Dec;27(1):54-65

Didymin/香蜂草苷 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Male BALB/c mice DOX-induced cardiotoxicity model Intraperitoneal injection 2, 4, 8 mg/kg Once daily for 7 days Did pretreatment significantly restored body weight, inhibited DOX-induced increase of LDH, CK, AST, and alleviated myocardial tissue injury and oxidative stress Chin Herb Med. 2021 Jul 15;14(1):70-78
C57BL/6J mice CCl4-induced liver fibrosis model Intragastric administration 2, 1, or 0.5 mg/kg 6 weeks Didymin significantly attenuated CCl4-induced hepatic injury and fibrogenesis, as evidenced by the ameliorative pathological tissue, low transaminase activity, and decreased collagen accumulation. Drug Des Devel Ther. 2022 Jun 7;16:1713-1729
C57BL/6J mice High-fat diet-induced impaired glucose tolerance (IGT) mouse model Intraperitoneal injection 0.8 mg/kg Once daily for three weeks To evaluate the effect of Didymin on pancreatic beta cell function in high-fat diet-induced IGT mice. Results showed that Didymin reduced postprandial glycemia and enhanced 30-minute postprandial insulin levels, improving pancreatic beta cell insulin secretion function. Diabetol Metab Syndr. 2024 Jan 3;16(1):7
C57BL/6J mice High-fat diet-induced MAFLD mouse model Intraperitoneal injection 0.8 mg/kg Once daily for three weeks To evaluate the therapeutic effect of Didymin on high-fat diet-induced MAFLD mice. Results showed that Didymin significantly reduced hepatic lipid deposition and serum lipid levels. J Transl Med. 2023 Dec 19;21(1):921
SD rats Not used Oral 25 mg/kg Single dose Evaluate the pharmacokinetic properties of Didymin and its inclusion complexes. Results showed that the bioavailability of Didymin/HP-β-CD inclusion complex was significantly higher than that of free Didymin and Didymin/β-CD inclusion complex. Drug Deliv. 2020 Dec;27(1):54-65

Didymin/香蜂草苷 参考文献

[1]Morelli S, Piscioneri A, et al. Neuroprotective effect of didymin on hydrogen peroxide-induced injury in the neuronal membrane system. Cells Tissues Organs. 2014;199(2-3):184-200.

[2]Singhal J, Nagaprashantha LD, et al. Didymin induces apoptosis by inhibiting N-Myc and upregulating RKIP in neuroblastoma. Cancer Prev Res (Phila). 2012 Mar;5(3):473-83.

Didymin/香蜂草苷 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.68mL

0.34mL

0.17mL

8.41mL

1.68mL

0.84mL

16.82mL

3.36mL

1.68mL

Didymin/香蜂草苷 技术信息

CAS号14259-47-3
分子式C28H34O14
分子量 594.56
SMILES Code O=C1C[C@@H](C2=CC=C(OC)C=C2)OC3=CC(O[C@H]4[C@@H]([C@H]([C@@H]([C@@H](CO[C@H]5[C@@H]([C@@H]([C@H]([C@H](C)O5)O)O)O)O4)O)O)O)=CC(O)=C13
MDL No. MFCD00151177
别名 香风草甙 ;Neoponcirin; Isosakuranetin-7-O-rutinoside
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: 250 mg/mL(420.48 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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