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。


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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。 | |||||||||||||||||||
| 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. |
| 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 |
| 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 |
| 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 |
|
| 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 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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