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7-O-Methylmorroniside is a chemical compound belonging to the iridoid monoterpenes family, predominantly found in the fruit of Cornus officinalis, a type of dogwood. It has been studied for its potential health benefits and is typically isolated for scientific research. 7-O-Methylmorroniside is suggested to possess properties beneficial for heart and liver health, anti-diabetic properties, and potential antioxidant activity, although further comprehensive research is required to fully elucidate its properties and applications.

41679-97-4

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41679-97-4 Usage

Uses

Used in Pharmaceutical Industry:
7-O-Methylmorroniside is used as a potential therapeutic agent for heart and liver health due to its suggested beneficial properties for these organs.
Used in Anti-diabetic Applications:
In the field of diabetes management, 7-O-Methylmorroniside is used as an anti-diabetic compound, potentially aiding in the regulation of blood sugar levels.
Used in Antioxidant Formulations:
7-O-Methylmorroniside is utilized as an antioxidant in formulations designed to combat oxidative stress and related conditions, capitalizing on its potential antioxidant activity.

Check Digit Verification of cas no

The CAS Registry Mumber 41679-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,7 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41679-97:
(7*4)+(6*1)+(5*6)+(4*7)+(3*9)+(2*9)+(1*7)=144
144 % 10 = 4
So 41679-97-4 is a valid CAS Registry Number.

41679-97-4Downstream Products

41679-97-4Relevant academic research and scientific papers

Iodine-catalyzed etherification of morroniside

Sunghwa, Fortunatus,Sakurai, Hiroaki,Saiki, Ikuo,Koketsu, Mamoru

, p. 112 - 115 (2009)

In this study, we describe a highly selective etherification procedure of unprotected morroniside catalyzed by molecular iodine in acetone. The etherification reaction furnished 7-O-alkyl ether derivatives in reasonable yields within few hours under neutr

Morroniside cinnamic acid conjugate as an anti-inflammatory agent

Takeda, Yoshinori,Tanigawa, Naomi,Sunghwa, Fortunatus,Ninomiya, Masayuki,Hagiwara, Makoto,Matsushita, Kenji,Koketsu, Mamoru

, p. 4855 - 4857 (2010)

A morroniside cinnamic acid conjugate was prepared and evaluated on E-selectin mediated cell-cell adhesion as an important role in inflammatory processes. 7-O-Cinnamoylmorroniside exhibited excellent anti-inflammatory activity (IC50 = 49.3 μM) by inhibiting the expression of E-selectin; further, it was more active than another cinnamic-acid-conjugated iridoid glycoside (harpagoside; IC50 = 88.2 μM), 7-O-methylmorroniside, and morroniside itself. As a result, 7-O- cinnamoylmorroniside was observed to be a potent inhibitor of TNF-α-induced E-selectin expression.

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