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Names | |||
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Preferred IUPAC name
(2S,2′R,3S,3′R)-3′-(3,5-Dihydroxyphenyl)-4-[(2S,3S,4R,5S)-4-(3,5-dihydroxyphenyl)-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-2,2′-bis(4-hydroxyphenyl)-2,2′,3,3′-tetrahydro[3,4′-bi-1-benzofuran]-6,6′-diol | |||
Other names
kob A
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Identifiers | |||
3D model (
JSmol)
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ChemSpider | |||
PubChem
CID
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CompTox Dashboard (
EPA)
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Properties | |||
C56H44O13 | |||
Molar mass | 924.94 g/mol | ||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Kobophenol A is a stilbenoid. It is a tetramer of resveratrol. It can be isolated from Caragana chamlagu, [1] from Caragana sinica [2] and from Carex folliculata seeds. [3]
The molecule shows a 2,3,4,5-tetraaryltetrahydrofuran skeleton. [3]
It has been shown to inhibit acetylcholinesterase. [1]
Acid-catalyzed epimerization of kobophenol A to carasinol B can be performed in vitro. [4]
| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
(2S,2′R,3S,3′R)-3′-(3,5-Dihydroxyphenyl)-4-[(2S,3S,4R,5S)-4-(3,5-dihydroxyphenyl)-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-2,2′-bis(4-hydroxyphenyl)-2,2′,3,3′-tetrahydro[3,4′-bi-1-benzofuran]-6,6′-diol | |||
Other names
kob A
| |||
Identifiers | |||
3D model (
JSmol)
|
|||
ChemSpider | |||
PubChem
CID
|
|||
CompTox Dashboard (
EPA)
|
|||
| |||
| |||
Properties | |||
C56H44O13 | |||
Molar mass | 924.94 g/mol | ||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Kobophenol A is a stilbenoid. It is a tetramer of resveratrol. It can be isolated from Caragana chamlagu, [1] from Caragana sinica [2] and from Carex folliculata seeds. [3]
The molecule shows a 2,3,4,5-tetraaryltetrahydrofuran skeleton. [3]
It has been shown to inhibit acetylcholinesterase. [1]
Acid-catalyzed epimerization of kobophenol A to carasinol B can be performed in vitro. [4]