 
        
        
        
                货号:A114540
                
                同义名:
                    
                        
                            槲皮素,二水
                            
                             / Sophoretin
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Quercetin Dihydrate是一种天然黄酮类化合物,可刺激重组SIRT1并抑制PI3K,其对PI3K γ、PI3K δ和PI3K β的IC50值分别为2.4 μM、3.0 μM和5.4 μM。
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| Type | HazMat fee for 500 gram (Estimated) | 
| Excepted Quantity | USD 0.00 | 
| Limited Quantity | USD 15-60 | 
| Inaccessible (Haz class 6.1), Domestic | USD 80+ | 
| Inaccessible (Haz class 6.1), International | USD 150+ | 
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ | 
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ | 
 
                                 
                                
                            

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| 产品名称 | C2β ↓ ↑ | p110α ↓ ↑ | p110β ↓ ↑ | p110γ ↓ ↑ | p110δ ↓ ↑ | PI3K ↓ ↑ | Vps34 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A66 | + C2β, IC50: 462 nM | ++ p110α, IC50: 32 nM | 99%+ | ||||||||||||||||
| Taselisib | + C2β, IC50: 292 nM | ++++ PI3Kα, Ki: 0.29 nM | +++ PI3Kβ, Ki: 9.1 nM | ++++ PI3Kγ, Ki: 0.97 nM | ++++ PI3Kδ, Ki: 0.12 nM | + hVps34, IC50: 374 nM | 99%+ | ||||||||||||
| Gedatolisib | ++++ PI3Kα, IC50: 0.4 nM | +++ PI3Kγ, IC50: 5.4 nM | mTOR | 99% | |||||||||||||||
| HS-173 | ++++ PI3Kα , IC50: 0.8 nM | 99%+ | |||||||||||||||||
| Serabelisib | +++ PI3Kα, IC50: 21 nM | 99%+ | |||||||||||||||||
| GNE-477 | ++++ PI3Kα, IC50: 4 nM | mTOR | 99% | ||||||||||||||||
| YM-201636 | + p110α, IC50: 3.3 μM | PIKfyve | 98% | ||||||||||||||||
| AS-252424 | + PI3Kα, IC50: 935 nM | ++ PI3Kγ, IC50: 33 nM | 99% | ||||||||||||||||
| Alpelisib | +++ PI3Kα, IC50: 5 nM | 99%+ | |||||||||||||||||
| AS-604850 | + PI3Kα, IC50: 4.5 μM | + PI3Kγ, IC50: 0.25 μM | 99% | ||||||||||||||||
| SF2523 | ++ PI3Kα, IC50: 34 nM | ++ PI3Kγ, IC50: 158 nM | mTOR,DNA-PK | 99%+ | |||||||||||||||
| Inavolisib | ++++ PI3K alpha, IC50: 0.038 nM | 99%+ | |||||||||||||||||
| Bimiralisib | ++++ PI3Kα, Kd: 1.5 nM | +++ PI3Kβ, Kd: 11 nM | ++ PI3Kγ, Kd: 25 nM | ++ PI3Kδ, Kd: 25 nM | mTOR | 99%+ | |||||||||||||
| GSK1059615 | ++++ PI3Kα, IC50: 0.4 nM | ++++ PI3Kβ, IC50: 0.6 nM | +++ PI3Kγ, IC50: 5 nM | ++++ PI3Kδ, IC50: 2 nM | mTOR | 98% | |||||||||||||
| GSK2636771 | ✔ | 99% | |||||||||||||||||
| Fimepinostat | +++ PI3Kα, IC50: 19 nM | ++ PI3Kβ, IC50: 54 nM | ++ PI3Kδ, IC50: 39 nM | 99%+ | |||||||||||||||
| VS-5584 | ++++ PI3Kα, IC50: 2.6 nM | +++ PI3Kβ, IC50: 21 nM | ++++ PI3Kγ, IC50: 3.0 nM | ++++ PI3Kδ, IC50: 2.7 nM | mTOR | 98% | |||||||||||||
| Dactolisib | ++++ p110α1, IC50: 4 nM | ++ p110β, IC50: 75 nM | +++ p110γ, IC50: 5 nM | +++ p110δ, IC50: 7 nM | 98+% | ||||||||||||||
| PI-103 | ++++ p110α, IC50: 2 nM | ++++ p110β, IC50: 3 nM | +++ p110γ, IC50: 15 nM | ++++ p110δ, IC50: 3 nM | mTOR,DNA-PK | 99%+ | |||||||||||||
| PI-3065 | + p110β, IC50: 1078 nM | +++ p110δ, IC50: 15 nM | 99%+ | ||||||||||||||||
| Voxtalisib | ++ PI3Kα, IC50: 39 nM | ++ PI3Kβ, IC50: 113 nM | +++ PI3Kγ, IC50: 9 nM | ++ PI3Kδ, IC50: 43 nM | mTOR,DNA-PK | 99%+ | |||||||||||||
| AZD-8835 | +++ PI3Kα, IC50: 6.2 nM | + PI3Kβ, IC50: 431 nM | ++ PI3Kγ, IC50: 90 nM | +++ PI3Kδ, IC50: 5.7 nM | 99% | ||||||||||||||
| Pilaralisib analogue | ++ PI3Kα, IC50: 39 nM | ++ PI3Kβ, IC50: 36 nM | +++ PI3Kγ, IC50: 23 nM | ++ PI3Kδ, IC50: 36 nM | 99%+ | ||||||||||||||
| ZSTK474 | +++ PI3Kα, IC50: 16 nM | ++ PI3Kβ, IC50: 44 nM | ++ PI3Kγ, IC50: 49 nM | +++ PI3Kδ, IC50: 4.6 nM | ++ PI3K, IC50: 37 nM | 98% | |||||||||||||
| AS-605240 | ++ PI3Kα, IC50: 60 nM | + PI3Kβ, IC50: 270 nM | +++ PI3Kγ, IC50: 8 nM | + PI3Kδ, IC50: 300 nM | 98% | ||||||||||||||
| TGX-221 | +++ p110β, IC50: 5 nM | ++ p110δ, IC50: 0.1 μM | 99%+ | ||||||||||||||||
| PF-04691502 | ++++ PI3Kα, Ki: 1.8 nM | ++++ PI3Kβ, Ki: 2.1 nM | ++++ PI3Kγ, Ki: 1.9 nM | ++++ PI3Kδ, Ki: 1.6 nM | mTOR | 98+% | |||||||||||||
| GDC-0084 | ++++ PI3Kα, Ki app: 2 nM | ++ PI3Kβ, Ki app: 46 nM | +++ PI3Kγ, Ki app: 10 nM | ++++ PI3Kδ, Ki app: 3 nM | mTOR | 99%+ | |||||||||||||
| Buparlisib | ++ p110α, IC50: 52 nM | + p110β, IC50: 166 nM | + p110γ, IC50: 262 nM | ++ p110δ, IC50: 116 nM | + Vps34, IC50: 2.4 μM | mTOR | 98% | ||||||||||||
| LY294002 | + p110α, IC50: 0.5 μM | + p110β, IC50: 0.97 μM | + p110δ, IC50: 0.57 μM | DNA-PK | 99%+ | ||||||||||||||
| AZD 6482 | + PI3Kα, IC50: 870 nM | +++ PI3Kβ, IC50: 10 nM | ++ PI3Kδ, IC50: 80 nM | DNA-PK | 99%+ | ||||||||||||||
| Pictilisib | ++++ p110α, IC50: 3 nM | ++ p110β, IC50: 33 nM | ++ p110γ, IC50: 75 nM | ++++ p110δ, IC50: 3 nM | mTOR | 99%+ | |||||||||||||
| PKI-402 | ++++ PI3Kα, IC50: 2 nM | +++ PI3Kβ, IC50: 7 nM | +++ PI3Kγ, IC50: 16 nM | +++ PI3Kδ, IC50: 14 nM | mTOR | 98% | |||||||||||||
| Copanlisib | ++++ PI3Kα, IC50: 0.5 nM | ++++ PI3Kβ, IC50: 3.7 nM | +++ PI3Kγ, IC50: 6.4 nM | ++++ PI3Kδ, IC50: 0.7 nM | 99%+ | ||||||||||||||
| Omipalisib | ++++ p110α, Ki: 0.019 nM | ++++ p110β, Ki: 0.13 nM | ++++ p110γ, Ki: 0.06 nM | ++++ p110δ, Ki: 0.024 nM | 99%+ | ||||||||||||||
| Izorlisib | +++ PI3Kα, IC50: 14 nM | ++ PI3Kβ, IC50: 0.12 μM | ++ PI3Kγ, IC50: 36 nM | + PI3Kδ, IC50: 0.50 μM | 99%+ | ||||||||||||||
| AZD8186 | ++ PI3Kα, IC50: 35 nM | ++++ PI3Kβ, IC50: 4 nM | +++ PI3Kδ, IC50: 12 nM | 99% | |||||||||||||||
| KU-0060648 | ++++ PI3Kα, IC50: 4 nM | ++++ PI3Kβ, IC50: 0.5 nM | + PI3Kγ, IC50: 0.59 μM | ++++ PI3Kδ, IC50: 0.1 nM | DNA-PK | 98% | |||||||||||||
| Apitolisib | +++ p110α, IC50: 5 nM | ++ p110β, IC50: 27 nM | +++ p110γ, IC50: 14 nM | +++ p110δ, IC50: 7 nM | mTOR | 98%+ | |||||||||||||
| CZC24832 | + PI3Kβ, IC50: 1.1 μM | ++ PI3Kγ, IC50: 27 nM | 98+% | ||||||||||||||||
| BGT226 maleate | ++++ PI3Kα, IC50: 4 nM | ++ PI3Kβ, IC50: 63 nM | ++ PI3Kγ, IC50: 38 nM | mTOR | 99%+ | ||||||||||||||
| TG 100713 | ++ PI3Kα, IC50: 165 nM | + PI3Kβ, IC50: 215 nM | ++ PI3Kγ, IC50: 50 nM | +++ PI3Kδ, IC50: 24 nM | 98%+ | ||||||||||||||
| PI3K-IN-1 | ++ PI3Kα, IC50: 39 nM | ++ PI3Kβ, IC50: 113 nM | +++ PI3Kγ, IC50: 9 nM | ++ PI3Kδ, IC50: 43 nM | mTOR,DNA-PK | 98+% | |||||||||||||
| TG100-115 | + PI3Kα, IC50: 1.3 μM | + PI3Kβ, IC50: 1.2 μM | ++ PI3Kγ, IC50: 83 nM | + PI3Kδ, IC50: 235 nM | 98% | ||||||||||||||
| PIK-90 | +++ PI3Kα, IC50: 11 nM | + PI3Kβ, IC50: 350 nM | +++ PI3Kγ, IC50: 18 nM | ++ PI3Kδ, IC50: 58 nM | 99%+ | ||||||||||||||
| PIK-294 | + p110β, IC50: 490 nM | ++ p110γ, IC50: 160 nM | +++ p110δ, IC50: 10 nM | 99%+ | |||||||||||||||
| Duvelisib | ++++ PI3Kβ, Ki: 1564 pM | ++ PI3Kγ, Ki: 243 pM | ++++ PI3Kδ, Ki: 23 pM | 99%+ | |||||||||||||||
| GDC-0326 | ++++ PI3Kα, Ki: 0.2 nM | ++ PI3Kβ, Ki: 26.6 nM | +++ PI3Kγ, Ki: 10.2 nM | ++++ PI3Kδ, Ki: 4 nM | 98% | ||||||||||||||
| Quercetin Dihydrate | + PI3Kβ, IC50: 5.4 μM | + PI3Kγ, IC50: 2.4 μM | + PI3Kδ, IC50: 3.0 μM | 95% | |||||||||||||||
| Quercetin | + PI3Kβ, IC50: 5.4 μM | + PI3Kγ, IC50: 2.4 μM | + PI3Kδ, IC50: 3.0 μM | Src,Sirtuin,PKC | 95% | ||||||||||||||
| Leniolisib | + PI3Kα, IC50: 0.244 μM | + PI3Kβ, IC50: 0.424 μM | + PI3Kγ, IC50: 2.23 μM | +++ PI3Kδ, IC50: 0.011 μM | DNA-PK | 99%+ | |||||||||||||
| PIK-108 | ✔ | 99% | |||||||||||||||||
| Eganelisib | +++ PI3Kγ, IC50: 16 nM | 99%+ | |||||||||||||||||
| CAY10505 | ✔ | 99% | |||||||||||||||||
| IPI-3063 | ++++ p110δ, IC50: 2.5 nM | 99% | |||||||||||||||||
| Nemiralisib | ++++ PI3Kδ, pKi: 9.9 | 99%+ | |||||||||||||||||
| PF-4989216 | ++++ p110α, IC50: 2 nM | ++ p110γ, IC50: 65 nM | ++++ p110δ, IC50: 1 nM | 99%+ | |||||||||||||||
| PIK-75 HCl | +++ p110α, IC50: 5.8 nM | ++ p110γ, IC50: 76 nM | + p110δ, IC50: 0.51 μM | DNA-PK | 99%+ | ||||||||||||||
| Tenalisib | ++ PI3Kγ, IC50: 33.2 nM | ++ PI3Kδ, IC50: 24.5 nM | 98% | ||||||||||||||||
| Acalisib | +++ p110δ, IC50: 14 nM | 99%+ | |||||||||||||||||
| Umbralisib | +++ PI3Kδ, IC50: 22.2 nM | 99%+ | |||||||||||||||||
| AMG319 | + PI3Kγ, IC50: 850 nM | +++ PI3Kδ, IC50: 18 nM | 99% | ||||||||||||||||
| IC-87114 | + PI3Kγ, IC50: 29 μM | + PI3Kδ, IC50: 0.5 μM | 99%+ | ||||||||||||||||
| Idelalisib | ++ p110γ, IC50: 89 nM | ++++ p110δ, IC50: 2.5 nM | 98% | ||||||||||||||||
| PIK-293 | + p110γ, IC50: 10 μM | + p110δ, IC50: 0.24 μM | 99%+ | ||||||||||||||||
| Vps34-PIK-III | + PI3Kδ, IC50: 1.2μM | +++ Vps34, IC50: 0.018μM | 99%+ | ||||||||||||||||
| GSK2292767 | ✔ | 98% | |||||||||||||||||
| Seletalisib | + PI3Kγ, IC50: 282 nM | +++ PI3Kδ, IC50: 12 nM | 99%+ | ||||||||||||||||
| P110δ-IN-1 | ++++ P110δ, IC50: 0.6 nM | 99% | |||||||||||||||||
| PI3Kδ-IN-5 | ++++ PI3Kδ, IC50: 0.9 nM | 99% | |||||||||||||||||
| SRX3207 | + PI3K alpha, IC50: 244 nM | + PI3K gamma, IC50: 9790 nM | + PI3K delta, IC50: 388 nM | Syk | 98% | ||||||||||||||
| Parsaclisib HCl | ++++ PI3Kδ, IC50: 1 nM | 98% | |||||||||||||||||
| IHMT-PI3Kδ-372 | +++ PI3Kδ, IC50: 14 nM | 98% | |||||||||||||||||
| Trigonelline | ✔ | Akt | 99%+ | ||||||||||||||||
| Wortmannin | ++++ PI3K, IC50: 3 nM | MLCK,DNA-PK | 99%+ | ||||||||||||||||
| Samotolisib | ✔ | DNA-PK | 99%+ | ||||||||||||||||
| GNE-317 | ✔ | 99%+ | |||||||||||||||||
| Oroxin B | ✔ | PTEN,Akt | 99%+ | ||||||||||||||||
| NU 7026 | + PI3K, IC50: 13 μM | DNA-PK | 98+% | ||||||||||||||||
| Deguelin | ✔ | Akt | 99%+ | ||||||||||||||||
| Ailanthone | ✔ | ATM/ATR,CDK,Akt | 98% | ||||||||||||||||
| Resibufogenin | ✔ | ROS | 98% | ||||||||||||||||
| KU-57788 | + PI3K, IC50: 5 μM | mTOR,DNA-PK | 99%+ | ||||||||||||||||
| Cinobufagine | ✔ | Akt | 99% | ||||||||||||||||
| α-Linolenic acid | ✔ | 97% (GC) | |||||||||||||||||
| MTX-211 | ✔ | EGFR | 98% | ||||||||||||||||
| PI3K/mTOR Inhibitor-2 | ++++ PI3K, IC50: 3.4 nM | mTOR | 99%+ | ||||||||||||||||
| SPP-86 | ✔ | 99%+ | |||||||||||||||||
| (E)-Akt inhibitor-IV | ✔ | 98% | |||||||||||||||||
| Vps34-IN-1 | ++ Vps34, IC50: 25 nM | 98% | |||||||||||||||||
| SAR405 | ++++ Vps34, IC50: 1.2 nM | 98+% | |||||||||||||||||
| 3-Methyladenine | + PI3Kγ, IC50: 60 μM | + Vps34, IC50: 25 μM | Autophagy | 98% | |||||||||||||||
| Vps34-IN-4 | +++ VPS34, IC50: 15 nM | 98%+ | |||||||||||||||||
| Autophinib | +++ Vps34, IC50: 19 nM | Autophagy | 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。 | |||||||||||||||||||
| 靶点 | 
 | 
| 描述 | Quercetin is a natural flavonoid that can activate SIRT1, inhibit PI3K, inhibit PI3K γ, PI3K δ, PI3K β, with IC50[3]. In vitro,the IC50[4]. In vivo, combination of quercetin and 2-ME can serve as a novel clinical treatment regimen owning the potential of enhancing antitumor effect on prostate cancer and lessening the dose and side effects of either quercetin or 2-ME alone[5]. | 
| Concentration | Treated Time | Description | References | |
| Human Periodontal Ligament Cells (hPDLCs) | 5 μM | 24 h | Quercetin at 5 μM strongly activated NRF2 signaling, alleviated oxidative damage and enhanced the antioxidant capacity of hPDLCs. | Drug Des Devel Ther. 2021 Aug 12;15:3509-3522. | 
| HK-2 human renal tubule epithelial cells | 5 μM | 48 h | Quercetin significantly reduced the accumulation of fibrosis- and inflammation-related proteins induced by IL-33, improved renal cell pyroptosis, and acted through the IL-33/ST2 pathway. | Antioxidants (Basel). 2022 Nov 13;11(11):2238. | 
| HEK293 cells | 10 μM | To investigate the inhibitory effect of Quercetin on hP2X3 receptors, results showed that Quercetin inhibited hP2X3 with an IC50 of 4.72 ± 0.35 μM. | Nat Commun. 2023 Sep 20;14(1):5844. | |
| HEK293 cells | 100 μM | To investigate the inhibitory effect of Quercetin on hP2X1, hP2X4, and hP2X7 receptors, results showed that Quercetin inhibited hP2X1 by 21.4 ± 5.0%, with almost no inhibition of hP2X4 and hP2X7. | Nat Commun. 2023 Sep 20;14(1):5844. | |
| ER-α/ER-β reporter cells | 0.023–50 µg/mL | 24 h | Quercetin had a small effect on ER-α but strongly activated ER-β, with an ER-β/ER-α specificity of 3.2. | Int J Mol Sci. 2021 Jan 21;22(3):1032. | 
| C2C12 skeletal muscle cells | 25, 50, 75, 100 µM | 24 h | Quercetin significantly increased the viability of dexamethasone-treated C2C12 skeletal muscle cells and exerted antiapoptotic effects by regulating mitochondrial membrane potential (ΔΨm) and reducing oxidative species. | Molecules. 2020 Jul 17;25(14):3267. | 
| AMJ2-C11 cells | 0, 5, 10, 20 μM | 4 or 8 h | To investigate the induction of HO-1 mRNA and protein expression by quercetin, results showed that quercetin dose-dependently induced HO-1 expression. | Respir Res. 2014 Nov 21;15(1):150. | 
| LA-4 cells | 0, 5, 10, 20 μM | 4 or 8 h | To investigate the induction of HO-1 mRNA and protein expression by quercetin, results showed that quercetin dose-dependently induced HO-1 expression. | Respir Res. 2014 Nov 21;15(1):150. | 
| HBEC4 cells | 0, 5, 10, 20 μM | 4 or 8 h | To investigate the induction of HO-1 mRNA and protein expression by quercetin, results showed that quercetin dose-dependently induced HO-1 expression. | Respir Res. 2014 Nov 21;15(1):150. | 
| MIN-6 cells | 10 μM | 1 h | To investigate the effect of Quercetin on insulin secretion, results showed that 10 μM Quercetin significantly increased insulin secretion in the presence of 8.3 mmol/L glucose. | Drug Des Devel Ther. 2018 Apr 23;12:955-966. | 
| MIN-6 cells | 10 μM | 24 h | To investigate the effect of Quercetin on palmitic acid-induced apoptosis in MIN-6 cells, results showed that 10 μM Quercetin significantly improved cell viability. | Drug Des Devel Ther. 2018 Apr 23;12:955-966. | 
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | Periodontitis model | Oral gavage | 50 mg/kg | Once daily for 10 days | Quercetin reduced oxidative stress levels and slowed alveolar bone absorption in periodontitis mice by activating the NRF2 signaling pathway. | Drug Des Devel Ther. 2021 Aug 12;15:3509-3522. | 
| MRL/lpr mice | Systemic lupus erythematosus (SLE) model | Oral gavage | 40 mg/kg | Once daily for three months | Quercetin improved renal function and inhibited the expression of fibrosis- and inflammation-related markers in MRL/lpr mice. | Antioxidants (Basel). 2022 Nov 13;11(11):2238. | 
| Mice | Sod1KO mice | Oral gavage | 50 mg/kg | Three consecutive days every 15 days for 7 months | To study the effect of D + Q on inflammation and hepatocellular carcinoma in the livers of Sod1KO mice. The results showed that D + Q significantly reduced markers of inflammation and the incidence of hepatocellular carcinoma in the livers of Sod1KO mice. | Aging Cell. 2022 Aug;21(8):e13676 | 
| C57BL/6 mice | Chronic cough model | Oral | 150 mg/kg | Twice daily for 7 days | To investigate the cough-relieving effect of Quercetin on chronic cough, results showed that 150 mg/kg Quercetin significantly reduced the frequency of coughing in mice. | Nat Commun. 2023 Sep 20;14(1):5844. | 
| Mice | Triple-transgenic Alzheimer's disease model mice | Oral | 100 mg/kg | Every 48 hours for one year | To evaluate the effect of long-term oral administration of Quercetin on neurodegeneration markers and cognitive function in triple-transgenic Alzheimer's disease model mice. The results showed that Quercetin significantly reduced β-amyloid aggregation and partially reduced tau hyperphosphorylation, thereby improving cognitive function in mice. | Molecules. 2019 Jun 20;24(12):2287 | 
| BALB/c mice | LPS-induced acute lung injury model | Intratracheal administration | 10μM,50μl | Single dose 6 hours before LPS challenge | To investigate the protective effects of quercetin on LPS-induced acute lung injury, results showed that quercetin pretreatment significantly attenuated LPS-induced pulmonary edema and inflammation. | Respir Res. 2014 Nov 21;15(1):150. | 
| Db/db mice | Type 2 diabetes model | Intragastric administration | 0.5 g/kg | Once daily for 4 weeks | To investigate the effect of Quercetin on glucose tolerance and insulin secretion in db/db mice, results showed that Quercetin significantly improved glucose tolerance and insulin secretion. | Drug Des Devel Ther. 2018 Apr 23;12:955-966. | 
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 | 
| NCT01881919 | Hyperuricemia ... 展开 >> Gout Kidney Calculi Diabetes Cardiovascular Disease 收起 << | Early Phase 1 | Completed | - | United Kingdom ... 展开 >> School of Food Science and Nutrition Leeds, West Yorkshire, United Kingdom, LS2 9JT 收起 << | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.96mL 0.59mL 0.30mL | 14.78mL 2.96mL 1.48mL | 29.56mL 5.91mL 2.96mL | |
| CAS号 | 6151-25-3 | 
| 分子式 | C15H14O9 | 
| 分子量 | 338.27 | 
| SMILES Code | O=C1C(O)=C(C2=CC=C(O)C(O)=C2)OC3=C1C(O)=CC(O)=C3.[H]O[H].[H]O[H] | 
| MDL No. | MFCD00149487 | 
| 别名 | 槲皮素,二水 ;Sophoretin | 
| 运输 | 蓝冰 | 
| InChI Key | GMGIWEZSKCNYSW-UHFFFAOYSA-N | 
| Pubchem ID | 5284452 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, room temperature | 
| 溶解方案 | DMSO: 105 mg/mL(310.41 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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			沪ICP备2024050318号-1