货号:A590254
同义名:
黄豆苷
/ Daidzoside; NPI-031D
Daidzin是一种从葛根(Pueraria lobata)根部提取的化合物,能抑制线粒体醛脱氢酶2(IC50=80 nM)和ALDH-I(Ki=20 nM),具有有效的抗动脉粥样硬化作用。


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| 靶点 |
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| 描述 | Daidzin is also a potent and selective inhibitor of human mitochondrial aldehyde dehydrogenase (ALDH-2) with IC50 of 80 nM[3]. Daidzin is also an isoflavone that has anti-oxidant, anti-carcinogenic, and anti-atherosclerotic activities[4]. Daidzin possess tyrosyl radical scavenging activity and thereby decreases the oxidative stress. Treatment with daidzin protects the cornea in dry eye rat model by suppression inflammation and oxidative stress[5]. ITG extract and its active component Daidzin effectively improved CYP-induced oxidative stress, inflammation, and fibrosis through inhibiting the MMP-8, TIMP-1, and oxidative stress[6]. Daidzin treatment (150 mg/kg per day i.p. for 6 days) significantly suppresses (> 70%) hamster ethanol intake but does not affect overall acetaldehyde metabolism. In vitro, daidzin suppresses hamster liver mitochondria-catalyzed acetaldehyde oxidation very potently with an IC50 value of 0.4 mM, which is substantially lower than the daidzin concentration (70 mM) found in the liver mitochondria of daidzin-treated hamsters[7]. Daidzin inhibits ALDH-I competitively with respect to formaldehyde with a Ki of 40 nM, and uncompetitively with respect to the coenzyme NAD+[8]. |
| Concentration | Treated Time | Description | References | |
| Hamster liver mitochondria | 0.4 μM | 10 min | To study the inhibitory effect of Daidzin on mitochondria-catalyzed acetaldehyde oxidation, results showed Daidzin significantly inhibited acetaldehyde oxidation with an IC50 of 0.4 μM. | Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8990-3 |
| neonatal rat cardiomyocytes | 20 µM | 48 h | To investigate the effect of Daidzin on mitochondrial membrane potential in cardiomyocytes under high glucose conditions. Results showed that high glucose treatment significantly decreased mitochondrial membrane potential, and Daidzin further exacerbated this effect. | Mol Med. 2011 Mar-Apr;17(3-4):172-9 |
| Neuro2A cells | 20 or 40 µM | 12 h | To study the effect of ALDH2 inhibition on alcohol-induced neuronal damage, results showed that Daidzin pretreatment exacerbated ethanol-induced cell viability reduction and oxidative stress-related PTMs. | Cells. 2024 May 28;13(11):927 |
| T84 human colon cells | 10 μM | 12 h | Pretreatment with Daidzin exacerbated ethanol-induced cell permeability and reduced TJ/AJ proteins in T84 human colon cells. These changes were reversed by Alda-1, an ALDH2 activator. | Redox Biol. 2023 Feb;59:102577. |
| Administration | Dosage | Frequency | Description | References | ||
| Syrian golden hamsters | Free-choice ethanol intake model | Intraperitoneal injection | 150 mg/kg/day | Once daily for 6 days | To study the effect of Daidzin on hamster ethanol intake and its impact on acetaldehyde metabolism, results showed Daidzin significantly suppressed ethanol intake (70%) without affecting acetaldehyde metabolism. | Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8990-3 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.40mL 0.48mL 0.24mL |
12.01mL 2.40mL 1.20mL |
24.02mL 4.80mL 2.40mL |
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| CAS号 | 552-66-9 |
| 分子式 | C21H20O9 |
| 分子量 | 416.38 |
| SMILES Code | OC1=CC=C(C2=COC(C=C(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)C=C4)=C4C2=O)C=C1 |
| MDL No. | MFCD00017466 |
| 别名 | 黄豆苷 ;Daidzoside; NPI-031D; Daidzein 7-glucoside; Daidzein 7-O-glucoside |
| 运输 | 蓝冰 |
| InChI Key | KYQZWONCHDNPDP-QNDFHXLGSA-N |
| Pubchem ID | 107971 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 250 mg/mL(600.42 mM),配合低频超声,并水浴加热至45℃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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