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1 References  













Kobophenol A






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From Wikipedia, the free encyclopedia
  

Kobophenol A
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

CAS Number

3D model (JSmol)
ChemSpider

PubChem CID

CompTox Dashboard (EPA)

  • InChI=1S/C56H44O13/c57-33-9-1-27(2-10-33)53-47(31-17-37(61)21-38(62)18-31)49-43(23-41(65)25-45(49)67-53)52-50-44(24-42(66)26-46(50)68-55(52)29-5-13-35(59)14-6-29)51-48(32-19-39(63)22-40(64)20-32)54(28-3-11-34(58)12-4-28)69-56(51)30-7-15-36(60)16-8-30/h1-26,47-48,51-66H/t47-,48+,51-,52+,53+,54-,55-,56-/m1/s1 ☒N

    Key: RAUCCLKIJHMTND-LUPMIFTGSA-N ☒N

  • InChI=1/C56H44O13/c57-33-9-1-27(2-10-33)53-47(31-17-37(61)21-38(62)18-31)49-43(23-41(65)25-45(49)67-53)52-50-44(24-42(66)26-46(50)68-55(52)29-5-13-35(59)14-6-29)51-48(32-19-39(63)22-40(64)20-32)54(28-3-11-34(58)12-4-28)69-56(51)30-7-15-36(60)16-8-30/h1-26,47-48,51-66H/t47-,48+,51-,52+,53+,54-,55-,56-/m1/s1

    Key: RAUCCLKIJHMTND-LUPMIFTGBD

  • Oc1ccc(cc1)[C@@H]4Oc2cc(O)cc(c2[C@H]4c3cc(O)cc(O)c3)[C@H]6c7c(O[C@@H]6c5ccc(O)cc5)cc(O)cc7[C@H]%10[C@H](O[C@H](c8ccc(O)cc8)[C@H]%10c9cc(O)cc(O)c9)c%11ccc(O)cc%11

Properties

Chemical formula

 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).

☒N verify (what is checkY☒N ?)

Infobox references

Kobophenol A is a stilbenoid. It is a tetramerofresveratrol. 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]

References

[edit]
  1. ^ a b (+)-α-Viniferin, a Stilbene Trimer from Caragana chamlague, Inhibits Acetylcholinesterase. Sang Hyun Sung, So Young Kang, Ki Yong Lee, Mi Jung Park, Jeong Hun Kim, Jong Hee Park, Young Chul Kim, Jinwoong Kim and Young Choong Kim, Biological & Pharmaceutical Bulletin, Vol. 25, 2002 [permanent dead link]
  • ^ Simultaneous determination of the contents of three stilbene oligomers in Caragana sinica collected in different seasons using an improved HPLC method. Shu Na; Zhou Hong; Hu Changqi, Biological & pharmaceutical bulletin, 2006, vol. 29, no4, pp. 608-612
  • ^ a b Identification and bioactivities of resveratrol oligomers and flavonoids from Carex folliculata seeds. Li L, Henry GE and Seeram NP, J Agric Food Chem., 26 August 2009, volume 57, issue 16, pages 7282-7287, doi:10.1021/jf901716j
  • ^ Acid-catalyzed Epimerization of Kobophenol A to Carasinol B. Kejun Cheng, Gaolin Liang and Changqi Hu, Molecules 2008, 13(4), 938-942

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Kobophenol_A&oldid=1103021986"
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    ●This page was last edited on 8 August 2022, at 01:49 (UTC).
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