Ambeed.cn

首页 / / / PI3K / Quercetin Dihydrate/二水槲皮素

Quercetin Dihydrate/二水槲皮素 {[allProObj[0].p_purity_real_show]}

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。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

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+
Quercetin Dihydrate/二水槲皮素 化学结构 CAS号:6151-25-3
Quercetin Dihydrate/二水槲皮素 化学结构
CAS号:6151-25-3
Quercetin Dihydrate/二水槲皮素 3D分子结构
CAS号:6151-25-3
Quercetin Dihydrate/二水槲皮素 化学结构 CAS号:6151-25-3
Quercetin Dihydrate/二水槲皮素 3D分子结构 CAS号:6151-25-3
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

Quercetin Dihydrate/二水槲皮素 纯度/质量文件 产品仅供科研

货号:A114540 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 >
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。

Quercetin Dihydrate/二水槲皮素 生物活性

靶点
  • p110γ

    PI3Kγ, IC50:2.4 μM

  • p110β

    PI3Kβ, IC50:5.4 μM

  • p110δ

    PI3Kδ, IC50:3.0 μM

  • SIRT1

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].

Quercetin Dihydrate/二水槲皮素 细胞实验

Cell Line
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.

Quercetin Dihydrate/二水槲皮素 动物实验

Species
Animal Model
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.

Quercetin Dihydrate/二水槲皮素 临床研究

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 <<

Quercetin Dihydrate/二水槲皮素 参考文献

[1]Dajas F. Life or death: neuroprotective and anticancer effects of quercetin. J Ethnopharmacol. 2012 Sep 28;143(2):383-96.

[2]Sing SE, Peterson RK. Assessing environmental risks for established invasive weeds: Dalmatian (Linaria dalmatica) and yellow (L. vulgaris) toadflax in North America. Int J Environ Res Public Health. 2011 Jul;8(7):2828-53.

[3]Navarro-Núñez L, Lozano ML, Martínez C, Vicente V, Rivera J. Effect of quercetin on platelet spreading on collagen and fibrinogen and on multiple platelet kinases. Fitoterapia. 2010 Mar;81(2):75-80. doi: 10.1016/j.fitote.2009.08.006. Epub 2009 Aug 15. PMID: 19686810.

[4]Yu XB, Liu XJ, Qian DH, Zhang JP, Hu ZL, Wu TM. [Inhibitory effects of protein kinase C inhibitors on tumor necrosis factor induced bovine pulmonary artery endothelial cell injuries]. Yao Xue Xue Bao. 1996;31(3):176-81. Chinese. PMID: 9206266.

[5]Yang F, Song L, Wang H, Wang J, Xu Z, Xing N. Combination of Quercetin and 2-Methoxyestradiol Enhances Inhibition of Human Prostate Cancer LNCaP and PC-3 Cells Xenograft Tumor Growth. PLoS One. 2015 May 26;10(5):e0128277. doi: 10.1371/journal.pone.0128277. PMID: 26011145; PMCID: PMC4444352.

Quercetin Dihydrate/二水槲皮素 实验方案

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

Quercetin Dihydrate/二水槲皮素 技术信息

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

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。