7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560)

ChEBI > Main

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone

ChEBI ID	CHEBI:137560

Definition	An epoxide fluorescent probe for use in in vivo visualization of hydrogen sulfide. The probe employs a fluorescein as a fluorophore, and is equipped with an operating epoxide unit. FEPO functions via epoxide ring opening via nucleophilic attack by H2S.

Stars	This entity has been manually annotated by the ChEBI Team.

Submitter	Ceri

Supplier Information

Download	Molfile XML SDF

Formula

C26H20O7

Net Charge

Average Mass

444.434

Monoisotopic Mass

444.12090

InChI

InChI=1S/C26H20O7/c27-15-5-7-21-23(9-15)33-24-10-16(29-11-17-12-30-17)6-8-22(24)25(21)19-3-1-2-4-20(19)26(28)32-14-18-13-31-18/h1-10,17-18H,11-14H2

InChIKey

WWXWRWHYGBFEST-UHFFFAOYSA-N

SMILES

C=1C2=C(C=C(C1)OCC3CO3)OC=4C(=C2C=5C=CC=CC5C(=O)OCC6CO6)C=CC(C4)=O

Roles Classification
Application(s):	fluorescent probe A role played by a fluorescent molecular entity used to study the microscopic environment by fluorescence spectroscopy. dye (via xanthene dye )

ChEBI Ontology
Outgoing	7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560) has functional parent fluorescein (acid form) (CHEBI:172923) 7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560) has role fluorescent probe (CHEBI:39442) 7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560) is a aromatic ether (CHEBI:35618) 7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560) is a benzoate ester (CHEBI:36054) 7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560) is a epoxide (CHEBI:32955) 7-glycidyloxy-9-(2-glycidyloxycarbonylphenyl)-2-xanthone (CHEBI:137560) is a xanthene dye (CHEBI:37929)

IUPAC Name

(oxiran-2-yl)methyl 2-{6-[(oxiran-2-yl)methoxy]-3-oxo-3H-xanthen-9-yl}benzoate

Synonym	Source
FEPO	SUBMITTER

Registry Number	Type	Source
8516795	Reaxys Registry Number	Reaxys

Citation	Type	Source
25660659	PubMed citation	Europe PMC

Last Modified

18 May 2021