Movatterモバイル変換

[0]ホーム
URL:

Jump to content
WikipediaThe Free Encyclopedia
Search

Glyceollin III

From Wikipedia, the free encyclopedia
Glyceollin III
Chemical structure of glyceollin III
Chemical structure of glyceollin III
Names
Preferred IUPAC name
(2S,6aS,11aS)-2-(Prop-1-en-2-yl)-1,2-dihydro-6H-[1]benzofuro[3,2-c]furo[3,2-g][1]benzopyran-6a,9(11aH)-diol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • InChI=1S/C20H18O5/c1-10(2)15-6-11-5-13-17(8-16(11)24-15)23-9-20(22)14-4-3-12(21)7-18(14)25-19(13)20/h3-5,7-8,15,19,21-22H,1,6,9H2,2H3/t15-,19-,20+/m0/s1
    Key: MIYTVBARXCVVHZ-RYGJVYDSSA-N
  • CC(=C)[C@@H]1Cc2cc3c(cc2O1)OC[C@@]4([C@H]3Oc5c4ccc(c5)O)O
Properties
C20H18O5
Molar mass338.35 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Glyceollin III is aglyceollin, a type ofpterocarpan, found in the soybean (Glycine max).[1][2] It has anantiestrogenic effect.[3] In soil, it has anantifungal activity againstAspergillus sojae.[4]

References

[edit]
  1. ^Zimmermann, M. Carla; Tilghman, Syreeta L.; Boué, Stephen M.; Salvo, Virgilio A.; Elliott, Steven; Williams, K. Y.; Skripnikova, Elena V.; Ashe, Hasina; Payton-Stewart, Florastina; Vanhoy-Rhodes, Lyndsay; Fonseca, Juan Pablo; Corbitt, Cynthia; Collins-Burow, Bridgette M.; Howell, Melanie H.; Lacey, Michelle; Shih, Betty Y.; Carter-Wientjes, Carol; Cleveland, Thomas E.; McLachlan, John A.; Wiese, Thomas E.; Beckman, Barbara S.; Burow, Matthew E. (2010)."Glyceollin I, a Novel Antiestrogenic Phytoalexin Isolated from Activated Soy".Journal of Pharmacology and Experimental Therapeutics.332 (1):35–45.doi:10.1124/jpet.109.160382.PMC 2802480.PMID 19797619.
  2. ^Banks, Stephen W.; Dewick, Paul M. (1983). "Biosynthesis of glyceollins I, II and III in soybean".Phytochemistry.22 (12):2729–2733.doi:10.1016/S0031-9422(00)97682-9.
  3. ^Salvo Virgilo A., Boue Stephen M., Fonseca Juan P., Elliott Steven, Corbitt Cynthia, Collins-Burow Bridgette M., Curiel Tyler J., Srivastav Sudesh K., Shih Betty Y., Carter-Wientjes Carol, Wood Charles E., Erhardt Paulw., Beckman Barbara S., McLachlan John A., Cleveland Thomas E. and Burow Matthew E. (2006)."Antiestrogenic glyceollins suppress human breast and ovarian carcinoma tumorigenesis".Clinical Cancer Research.12 (23):7159–7164.doi:10.1158/1078-0432.CCR-06-1426.PMID 17145841.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^Kim, Hyo Jung; Suh, Hwa-Jin; Lee, Choong Hwan; Kim, Jeong Hwan; Kang, Sun Chul; Park, Sunmin; Kim, Jong-Sang (2010). "Antifungal Activity of Glyceollins Isolated from Soybean Elicited with Aspergillus sojae".Journal of Agricultural and Food Chemistry.58 (17):9483–9487.doi:10.1021/jf101694t.PMID 20666365.
Types of pterocarpans
Pterocarpans:
O-methylated
Prenylated
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


Stub icon

This article about anaromatic compound is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Glyceollin_III&oldid=1292490171"
Categories:
Hidden categories:
[8]ページ先頭
©2009-2025 Movatter.jp