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Wikipedia

Gallocatechol

Gallocatechol or gallocatechin (GC) is a flavan-3-ol, a type of chemical compound including catechin, with the gallate residue being in an isomeric trans position.

Gallocatechol
Names
Other names
(+)-gallocatechin
Identifiers
  • 970-73-0 N
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:68330 N
ChEMBL
  • ChEMBL47386 N
ChemSpider
  • 58594 N
KEGG
  • C12127
MeSH Gallocatechol
  • 65084
UNII
  • HEJ6575V1X N
  • InChI=1S/C15H14O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-4,12,15-21H,5H2/t12-,15+/m0/s1 N
    Key: XMOCLSLCDHWDHP-SWLSCSKDSA-N N
  • InChI=1/C15H14O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-4,12,15-21H,5H2/t12-,15+/m0/s1
    Key: XMOCLSLCDHWDHP-SWLSCSKDBQ
  • C1[C@@H]([C@H](OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O
Properties
C15H14O7
Molar mass 306.270 g·mol−1
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 ?)

This compound possesses two epimers. The most common, (+)-gallocatechin (GC), CAS number 970-73-0, is found notably in green tea. The other enantiomer is called (-)-gallocatechin or ent-gallocatechin. It was first isolated from green tea by Michiyo Tsujimura in 1934.[1]

Epigallocatechin is another type of catechin, with the gallate residue being in an isomeric cis position. It can be found in St John's wort.[2]

See also edit

References edit

  1. ^ "Michiyo Tsujimura (1888–1969)". Ochanomizu University. Retrieved 10 November 2015.
  2. ^ Wei, Yun; Xie, Qianqian; Dong, Wanting; Ito, Yoichiro (2009). "Separation of epigallocatechin and flavonoids from Hypericum perforatum L. By high-speed counter-current chromatography and preparative high-performance liquid chromatography". Journal of Chromatography A. 1216 (19): 4313–4318. doi:10.1016/j.chroma.2008.12.056. PMC 2777726. PMID 19150073.

External links edit

  • Epigallocatechin on the Sigma-Aldrich website
  • Gallocatechin on the Sigma-Aldrich website

gallocatechol, gallocatechin, flavan, type, chemical, compound, including, catechin, with, gallate, residue, being, isomeric, trans, position, namesother, names, gallocatechinidentifierscas, number, model, jsmol, interactive, imagechebi, chebi, 68330, nchembl,. Gallocatechol or gallocatechin GC is a flavan 3 ol a type of chemical compound including catechin with the gallate residue being in an isomeric trans position Gallocatechol NamesOther names gallocatechinIdentifiersCAS Number 970 73 0 N3D model JSmol Interactive imageChEBI CHEBI 68330 NChEMBL ChEMBL47386 NChemSpider 58594 NKEGG C12127MeSH GallocatecholPubChem CID 65084UNII HEJ6575V1X NInChI InChI 1S C15H14O7 c16 7 3 9 17 8 5 12 20 15 22 13 8 4 7 6 1 10 18 14 21 11 19 2 6 h1 4 12 15 21H 5H2 t12 15 m0 s1 NKey XMOCLSLCDHWDHP SWLSCSKDSA N NInChI 1 C15H14O7 c16 7 3 9 17 8 5 12 20 15 22 13 8 4 7 6 1 10 18 14 21 11 19 2 6 h1 4 12 15 21H 5H2 t12 15 m0 s1Key XMOCLSLCDHWDHP SWLSCSKDBQSMILES C1 C H C H OC2 CC CC C21 O O C3 CC C C C3 O O O OPropertiesChemical formula C 15H 14O 7Molar mass 306 270 g mol 1Except 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 references This compound possesses two epimers The most common gallocatechin GC CAS number 970 73 0 is found notably in green tea The other enantiomer is called gallocatechin or ent gallocatechin It was first isolated from green tea by Michiyo Tsujimura in 1934 1 Epigallocatechin is another type of catechin with the gallate residue being in an isomeric cis position It can be found in St John s wort 2 See also editEpigallocatechin gallate Prodelphinidin List of phytochemicals in foodReferences edit Michiyo Tsujimura 1888 1969 Ochanomizu University Retrieved 10 November 2015 Wei Yun Xie Qianqian Dong Wanting Ito Yoichiro 2009 Separation of epigallocatechin and flavonoids from Hypericum perforatum L By high speed counter current chromatography and preparative high performance liquid chromatography Journal of Chromatography A 1216 19 4313 4318 doi 10 1016 j chroma 2008 12 056 PMC 2777726 PMID 19150073 External links editEpigallocatechin on the Sigma Aldrich website Gallocatechin on the Sigma Aldrich website Retrieved from https en wikipedia org w index php title Gallocatechol amp oldid 1186954597, wikipedia, wiki, book, books, library,

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