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9,9'-Di-O-(E)-feruloylsecoisolariciresinol
9,9'-Di-O-(E)-feruloylsecoisolariciresinol
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 9,9'-Di-O-(E)-feruloylsecoisolariciresinol
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CAS No.: 56973-66-1
Catalog No.: CFN98956
Molecular Formula: C40H42O12
Molecular Weight: 714.8 g/mol
Purity: >=98%
Type of Compound: Lignans
Physical Desc.: Powder
Source: The herb of Betula ermanii.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: 1,4-O-Diferuloylsecoisolariciresinol(9,9'-Di-O-(E)-feruloylsecoisolariciresinol),and pierreione B, two novel inhibitors of mTOR signaling, have strong anticancer activity. (+)-9,9′-O-Diferuloylsecoisolariciresinol has significant cytotoxic activity against the DU145, LNCaP, and A549 cell lines.
Targets: mTOR
In vitro:
Chemistry of Natural Compounds, 2014, 50(6): 978-81.
Phytochemical Investigation and Cytotoxic Evaluation of Components of Leaves and Stems of Machilus zuihoensis var. mushaensis[Reference: WebLink]

METHODS AND RESULTS:
From the MeOH extract of the leaves and stems of Machilus zuihoensis var. mushaensis, one new lignan, machilolin-B (1), together with 10 known compounds, zuonin B (2), (+)-9,9′-O-diferuloylsecoisolariciresinol (9,9'-Di-O-(E)-feruloylsecoisolariciresinol,3), (E)-3-(3-hydroxybut-1-enyl)-2,4,4-trimethylcyclohexa-2,5-dienone (4), 5-[(1R,5R,8S)-8-hydroxy-1,5-dimethyl-3-oxo-6-oxabicyclo[3.2.1]oct-8-yl]-3-methyl-2,4-pentadienoic acid (5), vanillin (6), rhamnetin-3-O-β-D-galactopyranoside (7), 2-hydroxy-3,4-dioxopentanal (8), a mixture of β-sitosterol (9) and stigmasterol (10), and β-sitosteryl-β-D-glucoside (11), have been isolated.
CONCLUSIONS:
Among them, compound 3 was demonstrated to have significant cytotoxic activity against the DU145, LNCaP, and A549 cell lines. Compound 11 also possessed moderate antiproliferative activities against DU145 cell lines.
9,9'-Di-O-(E)-feruloylsecoisolariciresinol Description
Source: The herb of Betula ermanii.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

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
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.399 mL 6.995 mL 13.9899 mL 27.9799 mL 34.9748 mL
5 mM 0.2798 mL 1.399 mL 2.798 mL 5.596 mL 6.995 mL
10 mM 0.1399 mL 0.6995 mL 1.399 mL 2.798 mL 3.4975 mL
50 mM 0.028 mL 0.1399 mL 0.2798 mL 0.5596 mL 0.6995 mL
100 mM 0.014 mL 0.0699 mL 0.1399 mL 0.2798 mL 0.3497 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.
Protocol
Kinase Assay:
Cancer Chemother Pharmacol. 2013 Oct;72(4):799-808.
Identification of two novel inhibitors of mTOR signaling pathway based on high content screening.[Pubmed: 23934262]
Mammalian target of rapamycin (mTOR) signaling pathway plays a critical role in regulating cell growth, proliferation and survival. Dysregulation of mTOR signaling pathway is closely involved in cancer development and chemotherapy resistance. Inhibitors of mTOR signaling pathway have been demonstrated to be attractive therapeutics for cancer therapy. In the present study, we aim to discover novel mTOR signaling pathway inhibitors from a natural compound library.
METHODS AND RESULTS:
Inhibitors of mTOR signaling pathway were discovered via high content screen assay based on the subcellular localization of eukaryotic initiation factor 4E (eIF4E) in mouse embryonic fibroblast cells. Candidate compounds were further assessed in cancer cells. Phosphorylation levels of mTOR complexes downstream targets were analyzed using Western blot. Cell cytotoxicity and apoptosis were evaluated using MTS assay and flow cytometry, respectively. Two compounds, 1,4-O-diferuloylsecoisolariciresinol (9,9'-Di-O-(E)-feruloylsecoisolariciresinol,IM-1) and Pierreione B (IM-2), were identified which induced significant nuclear translocation of eIF4E in a panel of cancer cells. Both of the compounds decreased the phosphorylation levels of p70 ribosomal protein S6 kinase (S6K) and eIF4E binding protein 1 (4E-BP1), resulting in cancer cell cytotoxicity and apoptosis.
CONCLUSIONS:
Via high content screen assay, two novel inhibitors of mTOR signaling, IM-1 and IM-2, were identified with strong anticancer activity. IM-1 and IM-2 could be potential candidates for anticancer therapeutics by targeting mTOR signaling pathway and as such warrants further exploration.
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ar-Curcumene

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