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Glyceollin III

Glyceollin III is a glyceollin, a type of pterocarpan, found in the soybean (Glycine max).[1][2] It has an antiestrogenic effect.[3] In soil, it has an antifungal activity against Aspergillus sojae.[4]

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
  • 61080-23-7 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:52086 N
ChEMBL
  • ChEMBL2229450 N
ChemSpider
  • 10128488 N
KEGG
  • C15511 N
  • 11954193
UNII
  • 629FG6XLLL N
  • DTXSID20976571
  • 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 mass 338.35 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 YN ?)

References edit

  1. ^ Glyceollin I, a Novel Antiestrogenic Phytoalexin Isolated from Activated Soy. M. Carla Zimmermann, Syreeta L. Tilghman, Stephen M. Boué, Virgilio A. Salvo, Steven Elliott, K. Y. Williams, Elena V. Skripnikova, Hasina Ashe, Florastina Payton-Stewart, Lyndsay Vanhoy-Rhodes, Juan Pablo Fonseca, Cynthia Corbitt, Bridgette M. Collins-Burow, Melanie H. Howell, Michelle Lacey, Betty Y. Shih, Carol Carter-Wientjes, Thomas E. Cleveland, John A. McLachlan, Thomas E. Wiese, Barbara S. Beckman and Matthew E. Burow, JPET January 2010 vol. 332 no. 1, doi:10.1124/jpet.109.160382
  2. ^ Biosynthesis of glyceollins I, II and III in soybean. Stephen W. Banks and Paul M. Dewick, Phytochemistry, Volume 22, Issue 12, 1983, pp. 2729-2733, doi:10.1016/S0031-9422(00)97682-9
  3. ^ Antiestrogenic glyceollins suppress human breast and ovarian carcinoma tumorigenesis. 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., Clinical Cancer Research, 2006, vol. 12, no23, pp. 7159-7164
  4. ^ Antifungal Activity of Glyceollins Isolated from Soybean Elicited with Aspergillus sojae. Hyo Jung Kim, Hwa-Jin Suh, Choong Hwan Lee, Jeong Hwan Kim, Sun Chul Kang, Sunmin Park and Jong-Sang Kim, J. Agric. Food Chem., 2010, 58 (17), pp. 9483–9487, doi:10.1021/jf101694t


glyceollin, glyceollin, type, pterocarpan, found, soybean, glycine, antiestrogenic, effect, soil, antifungal, activity, against, aspergillus, sojae, namespreferred, iupac, name, 11as, prop, dihydro, benzofuro, furo, benzopyran, 11ah, diolidentifierscas, number. Glyceollin III is a glyceollin a type of pterocarpan found in the soybean Glycine max 1 2 It has an antiestrogenic effect 3 In soil it has an antifungal activity against Aspergillus sojae 4 Glyceollin III NamesPreferred 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 diolIdentifiersCAS Number 61080 23 7 Y3D model JSmol Interactive imageChEBI CHEBI 52086 NChEMBL ChEMBL2229450 NChemSpider 10128488 NKEGG C15511 NPubChem CID 11954193UNII 629FG6XLLL NCompTox Dashboard EPA DTXSID20976571InChI 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 s1Key MIYTVBARXCVVHZ RYGJVYDSSA NSMILES CC C C H 1Cc2cc3c cc2O1 OC C 4 C H 3Oc5c4ccc c5 O OPropertiesChemical formula C20H18O5Molar mass 338 35 g molExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox referencesReferences edit Glyceollin I a Novel Antiestrogenic Phytoalexin Isolated from Activated Soy M Carla Zimmermann Syreeta L Tilghman Stephen M Boue Virgilio A Salvo Steven Elliott K Y Williams Elena V Skripnikova Hasina Ashe Florastina Payton Stewart Lyndsay Vanhoy Rhodes Juan Pablo Fonseca Cynthia Corbitt Bridgette M Collins Burow Melanie H Howell Michelle Lacey Betty Y Shih Carol Carter Wientjes Thomas E Cleveland John A McLachlan Thomas E Wiese Barbara S Beckman and Matthew E Burow JPET January 2010 vol 332 no 1 doi 10 1124 jpet 109 160382 Biosynthesis of glyceollins I II and III in soybean Stephen W Banks and Paul M Dewick Phytochemistry Volume 22 Issue 12 1983 pp 2729 2733 doi 10 1016 S0031 9422 00 97682 9 Antiestrogenic glyceollins suppress human breast and ovarian carcinoma tumorigenesis 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 Clinical Cancer Research 2006 vol 12 no23 pp 7159 7164 Antifungal Activity of Glyceollins Isolated from Soybean Elicited with Aspergillus sojae Hyo Jung Kim Hwa Jin Suh Choong Hwan Lee Jeong Hwan Kim Sun Chul Kang Sunmin Park and Jong Sang Kim J Agric Food Chem 2010 58 17 pp 9483 9487 doi 10 1021 jf101694t nbsp This article about an aromatic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Glyceollin III amp oldid 1158082744, wikipedia, wiki, book, books, library,

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