CHEBI:136968 - 2-hydroxyestrone 2-O-(β-D-glucuronide)(1−)

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 2-hydroxyestrone 2-O-(β-D-glucuronide)(1−)
ChEBI ID CHEBI:136968
ChEBI ASCII Name 2-hydroxyestrone 2-O-(beta-D-glucuronide)(1-)
Definition A steroid glucuronide anion that is the conjugate base of 2-hydroxyestrone 2-O-(β-D-glucuronide) arising from deprotonation of the carboxylic acid function; major species at pH 7.3.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Nevila Nouspikel
Supplier Information
Download Molfile XML SDF
Formula C24H29O9
Net Charge -1
Average Mass 461.483
Monoisotopic Mass 461.18171
InChI InChI=1S/C24H30O9/c1-24-7-6-11-12(14(24)4-5-17(24)26)3-2-10-8-15(25)16(9-13(10)11)32-23-20(29)18(27)19(28)21(33-23)22(30)31/h8-9,11-12,14,18-21,23,25,27-29H,2-7H2,1H3,(H,30,31)/p-1/t11-,12+,14-,18-,19-,20+,21-,23+,24-/m0/s1
InChIKey DQNRWYSYNOPGQY-FKYASPJISA-M
SMILES C1[C@]2([C@]3([C@@](C4=C(C=C(O)C(=C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)C(=O)[O-])O)O)O)CC3)(CC[C@@]2(C(=O)C1)C)[H])[H])[H]
ChEBI Ontology
Outgoing 2-hydroxyestrone 2-O-(β-D-glucuronide)(1−) (CHEBI:136968) is a β-D-glucosiduronate (CHEBI:83411)
2-hydroxyestrone 2-O-(β-D-glucuronide)(1−) (CHEBI:136968) is a monocarboxylic acid anion (CHEBI:35757)
2-hydroxyestrone 2-O-(β-D-glucuronide)(1−) (CHEBI:136968) is a steroid glucosiduronic acid anion (CHEBI:136637)
2-hydroxyestrone 2-O-(β-D-glucuronide)(1−) (CHEBI:136968) is conjugate base of 2-hydroxyestrone 2-O-(β-D-glucuronide) (CHEBI:137957)
Incoming 2-hydroxyestrone 2-O-(β-D-glucuronide) (CHEBI:137957) is conjugate acid of 2-hydroxyestrone 2-O-(β-D-glucuronide)(1−) (CHEBI:136968)
IUPAC Name
3-hydroxy-17-oxoestra-1,3,5(10)-trien-2-yl β-D-glucopyranosiduronate
Synonyms Sources
2-hydroxyestrone 2-β-D-glucuronide(1−) ChEBI
2-hydroxyestrone 2-β-glucuronide(1−) ChEBI
2-hydroxyestrone 2-glucuronide ChEBI
2-OHE1 2G(1−) SUBMITTER
estrone 2-O-(β-D-glucuronate) UniProt
Citation Waiting for Citations Type Source
15472229 PubMed citation SUBMITTER
Last Modified
20 July 2017