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Vestitenone is a naturally occurring chemical compound found in the seeds of the African plant, Pterocarpus erinaceus, which is commonly known as the "African sandalwood." It is a member of the rotenoid family, a group of isoflavonoid compounds that exhibit various biological activities. Vestitenone has been studied for its potential anti-inflammatory, anti-cancer, and anti-malarial properties. The compound is known to inhibit the activity of certain enzymes, such as lipoxygenase and cyclooxygenase, which are involved in inflammation and pain. Additionally, vestitenone has shown promise in laboratory studies for its ability to disrupt the life cycle of the malaria parasite, making it a potential candidate for the development of new antimalarial drugs. However, further research is needed to fully understand its therapeutic potential and safety profile.

69401-36-1

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69401-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69401-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,0 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69401-36:
(7*6)+(6*9)+(5*4)+(4*0)+(3*1)+(2*3)+(1*6)=131
131 % 10 = 1
So 69401-36-1 is a valid CAS Registry Number.

69401-36-1Downstream Products

69401-36-1Relevant academic research and scientific papers

Odor-active constituents of Cedrus atlantica wood essential oil

Uehara, Ayaka,Tommis, Basma,Belhassen, Emilie,Satrani, Badr,Ghanmi, Mohamed,Baldovini, Nicolas

, p. 208 - 215 (2017/10/06)

The main odorant constituents of Cedrus atlantica essential oil were characterized by GC-Olfactometry (GC-O), using the Aroma Extract Dilution Analysis (AEDA) methodology with 12 panelists. The two most potent odor-active constituents were vestitenone and 4-acetyl-1-methylcyclohexene. The identification of the odorants was realized by a detailed fractionation of the essential oil by liquid-liquid basic extraction, distillation and column chromatography, followed by the GC-MS and GC-O analyses of some fractions, and the synthesis of some non-commercial reference constituents.

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