Cyphostemmin B: Difference between revisions
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|Section1={{Chembox Identifiers |
|Section1={{Chembox Identifiers |
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| CASNo = 220328-16-5 |
| CASNo = 220328-16-5 |
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| CASNo_Ref = <ref>{{cite journal |title=Cyphostemmin B {{!}} Chemical Substance Information {{!}} J-GLOBAL |journal= |
| CASNo_Ref = <ref>{{cite journal |title=Cyphostemmin B {{!}} Chemical Substance Information {{!}} J-GLOBAL |journal=Jglobal.JST.go.jp |url=https://jglobal.jst.go.jp/en/detail?JGLOBAL_ID=200907080892665358 |language=en}}</ref>{{Cascite|changed|}} |
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| ChEBI = 76192 |
| ChEBI = 76192 |
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| ChEMBL = 2335820 |
| ChEMBL = 2335820 |
Revision as of 10:54, 12 September 2021
Chemical structure of cyphostemmin B. | |
Names | |
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Other names
Quadrangularin A
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem CID
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Properties | |
C28H22O6 | |
Molar mass | 454.47 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cyphostemmin B is an oligostilbene found in Cyphostemma crotalarioides (Vitaceae).[2] It is a resveratrol dimer.
References
- ^ "Cyphostemmin B | Chemical Substance Information | J-GLOBAL". Jglobal.JST.go.jp.
- ^ Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae). Paul-Henri Ducrot, Albert Kollmann, Adil E. Bala, Amel Majira, Lucien Kerhoas, Robert Delorme and Jacques Einhorn, Tetrahedron Letters, Volume 39, Issue 52, 24 December 1998, Pages 9655–9658, doi:10.1016/S0040-4039(98)02207-2