
氧化芍药苷
Oxypaeoniflorin
|
产品编号 |
CFN99589 |
CAS编号 |
39011-91-1 |
分子式 = 分子量 |
C23H28O12 = 496.46 |
产品纯度 |
>=98% |
物理属性 |
Powder |
化合物类型 |
Monoterpenoids |
植物来源 |
The roots of Paeonia lactiflora Pall. |
ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用 |
|
产品名称 |
产品编号 |
CAS编号 |
包装 |
QQ客服 |
氧化芍药苷 |
CFN99589 |
39011-91-1 |
10mg |
QQ客服:1413575084 |
氧化芍药苷 |
CFN99589 |
39011-91-1 |
20mg |
QQ客服:1413575084 |
氧化芍药苷 |
CFN99589 |
39011-91-1 |
50mg |
QQ客服:1413575084 |
氧化芍药苷 |
CFN99589 |
39011-91-1 |
100mg |
QQ客服:1413575084 |
1. 在您收到产品后请检查产品。如无问题,请将产品存入冰霜并且样品瓶保持密封,产品可以存放长达24个月(2-8摄氏度)。
2. 只要有可能,产品溶解后,您应该在同一天应用于您的实验。 但是,如果您需要提前做预实验,或者需要全部溶解,我们建议您将溶液以等分试样的形式存放在-20℃的密封小瓶中。 通常,这些可用于长达两周。 使用前,打开样品瓶前,我们建议您将产品平衡至室温至少1小时。
3. 需要更多关于溶解度,使用和处理的建议? 请发送电子邮件至:service@chemfaces.com
订购流程
1. 在线订购
请联系我们QQ客服
2. 电话订购
请拨打电话:
027-84237683 或 027-84237783
3. 邮件或传真订购
发送电子邮件到: manager@chemfaces.com 或
发送传真到:027-84254680
提供订购信息
为了方便客户的订购,请需要订购ChemFaces产品的客户,在下单的时候请提供下列信息,以供我们快速为您建立发货信息。
1. 产品编号(CAS No.或产品名称)
2. 发货地址
3. 联系方法 (联系人,电话)
4. 开票抬头 (如果需要发票的客户)
5. 发票地址(发货地址与发票地址不同)
发货时间
1. 付款方式为100%预付款客户,我们将在确认收到货款后当天或1-3个工作日发货。
2. 付款方式为月结的客户,我们承诺在收到订单后当天或1-3个工作日内发货。
3. 如果客户所需要的产品,需要重新生产,我们有权告知客户,交货时间需要延期。
ChemFaces的产品在许多优秀和顶级科学期刊中被引用

Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.
IF=13.297(2019)PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)PMID: 30417089
我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
Complutense University of Madrid (Spain)
Shanghai Institute of Biochemistry and Cell Biology (China)
University of Limpopo (South Africa)
University of Helsinki (Finland)
CSIRO - Agriculture Flagship (Australia)
Semmelweis Unicersity (Hungary)
Research Unit Molecular Epigenetics (MEG) (Germany)
Centralised Purchases Unit (CPU), B.I.T.S (India)
University of the Basque Country (Spain)
Shanghai University of TCM (China)
Korea Intitute of Science and Technology (KIST) (Korea)
Heidelberg University (Germany)
Shanghai Institute of Organic Chemistry (China)
Utrecht University (Netherlands)
More...
国外学术期刊发表的引用ChemFaces产品的部分文献
Description: |
Oxypaeoniflorin in rat plasma and was successfully applied to pharmacokinetic study.
|
In vitro: |
Acta Biochim Pol . 2020 Jun 18;67(2):239-245. | Oxypaeoniflorin improves myocardial ischemia/reperfusion injury by activating the Sirt1/Foxo1 signaling pathway[Pubmed: 32550708] | Abstract
Myocardial ischemia/reperfusion (MI/R) injury is a leading cause of damage to cardiac tissues and is associated with high mortality and disability rates worldwide. Oxypaeoniflorin (OPA) has been found to be the main constituent of Paeonia veitchii Lynch. This study was conducted to explore the effect of OPA on MI/R injury and its potential mechanism. An in vivo MI/R injury model was established by transient coronary ligation in BALB/c mice, and an in vitro hypoxia/reoxygenation (H/R) injury model was established with rat cardiomyocyte H9c2 cells. Echocardiographic assessments demonstrated that OPA significantly reduced disruption of cardiac function and improved the indicators of ejection fraction (EF) and fractional shortening (FS). The enzyme-linked immunosorbent assay (ELISA) results suggested that OPA significantly reduced the release of myocardial infarction-related factors, such as the creatine kinase (CK-MB), cardiac troponin I (cTnI) and cardiac troponin T (cTnT). Additionally, hematoxylin-eosin (HandE) staining demonstrated that OPA markedly inhibited the myocardial apoptosis and necrosis caused by MI/R. Consistently, the results obtained from the cell counting kit-8 (CCK-8) and flow cytometry assays revealed that OPA obviously reversed the H/R-induced decrease in cell activity and increase in apoptosis of H9c2 cells. Furthermore, western blot assays indicated that OPA inhibited apoptosis by activating the Sirt1 (silent information regulator factor 2 related enzyme 1)/Foxo1(forkhead transcription factor FKHR) signaling pathway in myocardial tissues and H9c2 cells. Collectively, these novel findings are the first to provide strong evidence that OPA attenuates MI/R injury by activating the Sirt1 (silent information regulator factor 2 related enzyme 1)/Foxo1(forkhead transcription factor FKHR) signaling-mediated anti-apoptotic pathway. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
1 mM |
2.0143 mL |
10.0713 mL |
20.1426 mL |
40.2852 mL |
50.3565 mL |
5 mM |
0.4029 mL |
2.0143 mL |
4.0285 mL |
8.057 mL |
10.0713 mL |
10 mM |
0.2014 mL |
1.0071 mL |
2.0143 mL |
4.0285 mL |
5.0357 mL |
50 mM |
0.0403 mL |
0.2014 mL |
0.4029 mL |
0.8057 mL |
1.0071 mL |
100 mM |
0.0201 mL |
0.1007 mL |
0.2014 mL |
0.4029 mL |
0.5036 mL |
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
部分图片展示
联系方式
电机:027-84237783
传真:027-84254680
在线QQ: 1413575084
E-Mail:manager@chemfaces.com
湖北省武汉沌口经济技术开区车城南路83号1号楼第三层厂房

ChemFaces为科学家,科研人员与企业提供快速的产品递送。我们通过瑞士SGS ISO 9001:2008质量体系认证
天然化合物与对照品的研发和生产。