Leachianol G | CAS:164204-62-0 | Manufacturer ChemFaces

Leachianol G

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Size /Price /Stock	10 mM * 1 mL in DMSO / $368 / In-stock
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Description:

Reference standards.

In vitro:

J Agric Food Chem. 2007 Sep 19;55(19):7753-7.

Oligomers of resveratrol and ferulic acid prepared by peroxidase-catalyzed oxidation and their protective effects on cardiac injury.[Pubmed: 17696480 ]

METHODS AND RESULTS:
Peroxidase extracted from Momordica charantia was used for the oligomerization of trans-resveratrol and ferulic acid on a preparative scale. One new heterocoupling oligomer, trans-3 E-3-[(4-hydroxy-3-methoxyphenyl)methylene]-4-(3,5-dihydroxyphenyl)-5-(4-hydroxyphenyl)tetrahydro-2-franone (6), and six resveratrol dimers, Leachianol G (1), restrytisol B (2), parthenostilbenins A (3) and B (5), 7- O-acetylated Leachianol G (4), and resveratrol trans-dehydrodimer (8), and one known ferulic acid dehydrodimer, (3alpha,3aalpha,6alpha,6aalpha)tetrahydro-3,6-bis(4-hydroxy-3-methoxyphenyl)-1 H,4 H-furo[3,4-c]furan-1,4-dione (7) were obtained.
CONCLUSIONS:
Bioactive experiments showed that compounds 6- 8 have strong free radical scavenging effects and also have protective effects on doxorubicin-induced cardiac cell injury when tested in vitro.

Leachianol G Description

Source:	The roots of Ampelopsis brevipedunculata var. hancei
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.

Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

More...

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

Structure Identification:

Molecules. 2017 Mar 16;22(3). pii: E474.

Anti-Cancer Activity of Resveratrol and Derivatives Produced by Grapevine Cell Suspensions in a 14 L Stirred Bioreactor.[Pubmed: 28300789 ]

In the present study, resveratrol and various oligomeric derivatives were obtained from a 14 L bioreactor culture of elicited grapevine cell suspensions (Vitis labrusca L.).
METHODS AND RESULTS:
The crude ethyl acetate stilbene extract obtained from the culture medium was fractionated by centrifugal partition chromatography (CPC) using a gradient elution method and the major stilbenes contained in the fractions were subsequently identified by using a 13C-NMR-based dereplication procedure and further 2D NMR analyses including HSQC, HMBC, and COSY. Beside δ-viniferin (2), leachianol F (4) and Leachianol G (4'), four stilbenes (resveratrol (1), ε-viniferin (5), pallidol (3) and a newly characterized dimer (6)) were recovered as pure compounds in sufficient amounts to allow assessment of their biological activity on the cell growth of three different cell lines, including two human skin malignant melanoma cancer cell lines (HT-144 and SKMEL-28) and a healthy human dermal fibroblast HDF line. Among the dimers obtained in this study, the newly characterized resveratrol dimer (6) has never been described in nature and its biological potential was evaluated here for the first time.
CONCLUSIONS:
ε-viniferin as well as dimer (6) showed IC50 values on the three tested cell lines lower than the ones exerted by resveratrol and pallidol. However, activities of the first two compounds were significantly decreased in the presence of fetal bovine serum although that of resveratrol and pallidol was not. The differential tumor activity exerted by resveratrol on healthy and cancer lines was also discussed.

CAS No.	164204-62-0	Price	$368 / 5mg
Catalog No.	CFN95146	Purity	>=98%
Molecular Weight	472.5	Type of Compound	Phenols
Formula	C₂₈H₂₄O₇	Physical Description	Powder
Download	COA MSDS	Similar structural	Comparison (Web) (SDF)

Product Name	Leachianol G
CAS No.:	164204-62-0
Catalog No.:	CFN95146
Molecular Formula:	C₂₈H₂₄O₇
Molecular Weight:	472.5 g/mol
Purity:	>=98%
Type of Compound:	Phenols
Physical Desc.:	Powder
Source:	The roots of Ampelopsis brevipedunculata var. hancei
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:	$368 / 5mg

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Phenols Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	2.1164 mL	10.582 mL	21.164 mL	42.328 mL	52.9101 mL
5 mM	0.4233 mL	2.1164 mL	4.2328 mL	8.4656 mL	10.582 mL
10 mM	0.2116 mL	1.0582 mL	2.1164 mL	4.2328 mL	5.291 mL
50 mM	0.0423 mL	0.2116 mL	0.4233 mL	0.8466 mL	1.0582 mL
100 mM	0.0212 mL	0.1058 mL	0.2116 mL	0.4233 mL	0.5291 mL

CFN95146	Leachianol G	164204-62-0	472.5	C₂₈H₂₄O₇
CFN95147	Leachianol F	164123-50-6	472.5	C₂₈H₂₄O₇
CFN92340	Ampelopsin F	151487-08-0	454.5	C₂₈H₂₂O₆
CFN95148	Ampelopsin G	151487-09-1	680.7	C₄₂H₃₂O₉
CFN97075	Alboctalol	62394-00-7	488.5	C₂₈H₂₄O₈
CFN92854	Viniferin	253435-07-3	454.1	C₂₈H₂₂O₆
CFN92423	Gnetin D	84870-53-1	470.5	C₂₈H₂₂O₇
CFN92424	Shegansu B	291535-65-4	514.5	C₃₀H₂₆O₈
CFN92592	Bisisorhapontigenin A	865474-98-2	528.6	C₃₁H₂₈O₈
CFN92341	Pallidol	105037-88-5	454.5	C₂₈H₂₂O₆