De-O-methyllasiodiplodin

	产品编号	CFN96880
	CAS编号	32885-82-8
	分子式 = 分子量	C₁₆H₂₂O₄ = 278.34
	产品纯度	>=98%
	物理属性	Oil
	化合物类型	Phenols
	植物来源	The rhizomes of Smilax glabra.
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

提供自定义包装

产品名称	产品编号	CAS编号	包装	QQ客服
De-O-methyllasiodiplodin	CFN96880	32885-82-8	1mg	QQ客服：1457312923
De-O-methyllasiodiplodin	CFN96880	32885-82-8	5mg	QQ客服：1457312923
De-O-methyllasiodiplodin	CFN96880	32885-82-8	10mg	QQ客服：1457312923
De-O-methyllasiodiplodin	CFN96880	32885-82-8	20mg	QQ客服：1457312923

存储与注意事项

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

Universidad de La Salle (Mexico)

Universiti Putra Malaysia(UPM) (Malaysia)

Korea Food Research Institute(KFRI) (Korea)

Charles Sturt University (Denmark)

Institute of Chinese Materia Medica (China)

Uniwersytet Jagielloński w Krakowie (Poland)

Almansora University (Egypt)

University of Leipzig (Germany)

National Hellenic Research Foundation (Greece)

Korea Institute of Oriental Medicine (Korea)

Sanford Burnham Prebys Medical Discovery Institute (USA)

University of Melbourne (Australia)

Griffith University (Australia)

University of Queensland (Australia)

More...

Description:

De-O-methyllasiodiplodin exhibits radical scavenging, moderate antibacterial, and potential anti-inflammatory effects, it shows moderate suppression effects on induced NO production. De-O-methyllasiodiplodin effectively lowers the blood glucose level in db/db mice possibly via ameliorating the expression of obesity-related pro-inflammatory cytokines, highlighting the potential of the marine natural product as a drug lead for the treatment of metabolic disorders.

Targets:

IL Receptor | TNF-α | ROS | NO | Antifection

In vivo:

Acta Pharmacol Sin. 2013 Oct;34(10):1325-36.

Marine natural product des-O-methyllasiodiplodin effectively lowers the blood glucose level in db/db mice via ameliorating inflammation.[Pubmed: 23852084 ]

des-O-methyllasiodiplodin (De-O-methyllasiodiplodin,DML) from Cerbera manghas has shown antagonistic activity against mineralocorticoid receptor (MR). Considering the involvement of MR in the insulin tolerance, we attempted to investigate the potential of DML in the treatment of type 2 diabetes mellitus (T2DM).
METHODS AND RESULTS:
In HepG2 and 3T3-L1 cells, both H2O2 and aldosterone markedly stimulates the expression of MCP-1, TNFα, IL-6, p47 and PU.1 genes. Co-treatment with DML (10 μmol/L) significantly reduced the H2O2- or aldosterone-induced expression of these genes. SPR-based assay confirmed the antagonistic activity of DML against the interaction between SRC-1 and MR-LBD. Furthermore, DML decreased aldosterone-induced MR transcriptional activity in a dose-dependent manner. Downregulation of MR with siRNA in the cells prevented or significantly attenuated aldosterone-stimulated expression of these genes, whereas DML did no longer affect the expression of these genes except that of IL-6. Oral administration of DML effectively reduced the levels of blood glucose and glycosylated hemoglobin (HbA1c) in db/db mice. The treatment also rectified the expression of pro-inflammatory factor and ROS-related genes in db/db mice.
CONCLUSIONS:
DML effectively lowers the blood glucose level in db/db mice possibly via ameliorating the expression of obesity-related pro-inflammatory cytokines, highlighting the potential of the marine natural product as a drug lead for the treatment of metabolic disorders.

产品名称	产品编号	CAS编号	分子式 = 分子量	位单	联系QQ
二大花旋覆花内酯 B; Dibritannilactone B	CFN89501	1829580-18-8	C₃₄H₄₆O₉ = 598.72	5mg	QQ客服：2056216494
丹参酚酮; Salvinolone	CFN92243	120278-22-0	C₂₀H₂₆O₃ = 314.4	5mg	QQ客服：2159513211
GB 1a; GB 1a	CFN96934	220611-41-6	C₃₀H₂₂O₁₀ = 542.49	5mg	QQ客服：3257982914
5-羟基-8-(4-羟基苯基)-2,2-二甲基-2H,6H-苯并[1,2-B:5,4-B']二吡喃-6-酮; Carpachromene	CFN98969	57498-96-1	C₂₀H₁₆O₅ = 336.3	5mg	QQ客服：215959384

信息支持

公司简介
订购流程
付款方式
退换货政策

ChemFaces提供的产品仅用于科学研究使用，不用于诊断或治疗程序。

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。

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	3.5927 mL	17.9636 mL	35.9273 mL	71.8546 mL	89.8182 mL
5 mM	0.7185 mL	3.5927 mL	7.1855 mL	14.3709 mL	17.9636 mL
10 mM	0.3593 mL	1.7964 mL	3.5927 mL	7.1855 mL	8.9818 mL
50 mM	0.0719 mL	0.3593 mL	0.7185 mL	1.4371 mL	1.7964 mL
100 mM	0.0359 mL	0.1796 mL	0.3593 mL	0.7185 mL	0.8982 mL