Home>>Signaling Pathways>> Proteases>> Lipoxygenase>>S-(+)-Marmesin ((+)-Marmesin)

S-(+)-Marmesin ((+)-Marmesin) Sale

(Synonyms: 异紫花前胡内酯,(+)-Marmesin; (S)-Marmesin) 目录号 : GC30027

A coumarin with anticancer activity

S-(+)-Marmesin ((+)-Marmesin) Chemical Structure

Cas No.:13849-08-6

规格 价格 库存 购买数量
5 mg
¥1,080.00
现货
10 mg
¥1,800.00
现货
25 mg
¥3,600.00
现货
50 mg
¥6,210.00
现货
100 mg
¥8,910.00
现货

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

Description

Marmesin is a coumarin originally isolated from the mature bark of A. marmelos.1 Marmesin decreases proliferation and cell invasion induced by fetal bovine serum (FBS) in H1299 non-small cell lung cancer cells (NSCLCs) when used at a concentration of 10 ?M.2 It decreases VEGF secretion in A549 and H1299 cells and inhibits capillary-like structure formation by human umbilical vein endothelial cells (HUVECs). Marmesin also decreases proliferation of U937 human leukemia cells (IC50 = 40 ?M).3 It halts the cell cycle at the G2/M phase, increases the ratio of Bax to Bcl-2 protein, induces apoptosis, and inhibits cell migration. Marmesin reduces tumor growth in a U937 mouse xenograft model when administered at a dose of 30 mg/kg.

1.Chatterjee, A., and Mitra, S.S.On the constitution of the active principles isolated from the mature bark of Aegle marmelos, Corre?J. Am. Chem. Soc.71(2)606-609(1949) 2.Kim, J.H., Kim, M.S., Lee, B.H., et al.Marmesin-mediated suppression of VEGF/VEGFR and integrin β1 expression: Its implication in non-small cell lung cancer cell responses and tumor angiogenesisOncol. Rep.37(1)91-97(2017) 3.Dong, L., Xu, W.W., Li, H., et al.In vitro and in vivo anticancer effects of marmesin in U937 human leukemia cells are mediated via mitochondrial-mediated apoptosis, cell cycle arrest, and inhibition of cancer cell migrationOncol. Rep.39(2)597-602(2018)

化学性质

Cas No. 13849-08-6 SDF
别名 异紫花前胡内酯,(+)-Marmesin; (S)-Marmesin
Canonical SMILES O=C1C=CC2=CC3=C(O[C@H](C(C)(O)C)C3)C=C2O1
分子式 C14H14O4 分子量 246.26
溶解度 DMSO : 2 mg/mL (8.12 mM) 储存条件 Store at -20°C,protect from light
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 4.0607 mL 20.3037 mL 40.6075 mL
5 mM 0.8121 mL 4.0607 mL 8.1215 mL
10 mM 0.4061 mL 2.0304 mL 4.0607 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
给药剂量 mg/kg 动物平均体重 g 每只动物给药体积 ul 动物数量
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方)
% DMSO % % Tween 80 % saline
计算重置

产品文档

Quality Control & SDS

View current batch: