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(E)-2-hydroxy-3,5,3′,4′-tetramethoxystilbene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1182284-01-0

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1182284-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1182284-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,2,2,8 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1182284-01:
(9*1)+(8*1)+(7*8)+(6*2)+(5*2)+(4*8)+(3*4)+(2*0)+(1*1)=140
140 % 10 = 0
So 1182284-01-0 is a valid CAS Registry Number.

1182284-01-0Upstream product

1182284-01-0Downstream Products

1182284-01-0Relevant academic research and scientific papers

Effect of resveratrol-related stilbenoids on biomembrane models

Sarpietro, Maria Grazia,Spatafora, Carmela,Accolla, Maria Lorena,Cascio, Orazio,Tringali, Corrado,Castelli, Francesco

, p. 1424 - 1431 (2013)

The interactions of the two resveratrol analogues 2-hydroxy-3,5,3′, 5′-tetramethoxystilbene (4) and 2-hydroxy-3,5,3′,4′- tetramethoxystilbene (5) with model biomembranes were studied. The aim of this investigation was to highlight possible differences in the interactions with such biomembranes related to the minimal structural differences between these isomeric stilbenoids. In particular, different experiments on stilbenoid/biomembrane model systems using both differential scanning calorimetry (DSC) and Langmuir-Blodgett techniques were carried out to evaluate stilbenoid/multilamellar vesicle and stilbenoid/phospholipid monolayer interactions, respectively. Dimyristoylphosphatidylcholine was used as constituent of the biomembrane models and permitted the experiments to be carried out at 37 C, close to body temperature. Kinetic studies were also run by DSC to evaluate the uptake of the resveratrol derivatives by the biomembrane model in an aqueous medium and when transported by a lipophilic carrier. The results indicated that both of the resveratrol analogues influenced the behavior of multilamellar vesicles and monolayers, biomembrane models, with 4 producing a larger effect than 5. These results are useful for better understanding the mechanism of action of these compounds. Moreover, the kinetic results could be of importance for future design of lipophilic delivery systems for these stilbenoids.

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