(Q27145557)

Myricetin 3-O-glucuronide (English)

(2S,3S,4R,5R,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid

8 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₁H₁₈O₁₄

1 reference

Myricetin 3-O-glucuronide (English)

8 October 2016

canonical SMILES

C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O

1 reference

Myricetin 3-O-glucuronide (English)

8 October 2016

isomeric SMILES

C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)C(=O)O)O)O)O

1 reference

Simultaneous qualitative assessment and quantitative analysis of flavonoids in various tissues of lotus (Nelumbo nucifera) using high performance liquid chromatography coupled with triple quad mass spectrometry

Myricetin 3-O-glucuronide (English)

8 October 2016

1 reference

Cyclocarya paliurus

1 reference

Phenolic compounds from the leaves of Cyclocarya paliurus (Batal.) Ijinskaja and their inhibitory activity against PTP1B

Epilobium hirsutum

1 reference

Polyphenolic metabolites of Epilobium hirsutum

Melaleuca quinquenervia

1 reference

ChemInform Abstract: Flavonoids of Melaleuca quinquenervia.

Morella rubra

1 reference

A Triterpenoid and phenolic compounds from Myrica rubra seeds

Myrica rubra

1 reference

A Triterpenoid and phenolic compounds from Myrica rubra seeds

Chamaenerion dodonaei

1 reference

Concentrations of Myricetin 3-O-β-D-Glucuronide inEpilobium angustifoliumDuring Different Vegetation Stages and Evaluation of its Antiphlogistic Activity

Potentilla anserina

1 reference

Flavan-3-ols and flavonoids from Potentilla anserina

Epilobium dodonaei

1 reference

Concentrations of Myricetin 3-O-β-D-Glucuronide inEpilobium angustifoliumDuring Different Vegetation Stages and Evaluation of its Antiphlogistic Activity

Pistacia weinmannifolia

1 reference

Gallotannins and related polyphenols from Pistacia weinmannifolia

Oenothera biennis

1 reference

Chemical Composition, Antioxidative and Anti-Inflammatory Activity of Extracts Prepared from Aerial Parts of Oenothera biennis L. and Oenothera paradoxa Hudziok Obtained after Seeds Cultivation

Syzygium cumini

1 reference

Acylated flavonol glycosides from Eugenia jambolana leaves

Parkinsonia aculeata

1 reference

Chemical Composition and Biological Activities of the Aqueous Fraction of Parkinsonea aculeata L. Growing in Saudi Arabia

Identifiers

InChI

InChI=1S/C21H18O14/c22-6-3-7(23)11-10(4-6)33-17(5-1-8(24)12(26)9(25)2-5)18(13(11)27)34-21-16(30)14(28)15(29)19(35-21)20(31)32/h1-4,14-16,19,21-26,28-30H,(H,31,32)/t14-,15-,16+,19-,21+/m0/s1

1 reference

Myricetin 3-O-glucuronide (English)

8 October 2016

2 references

Myricetin 3-O-glucuronide (English)

8 October 2016

ChEBI release 2020-09-01

CAS Registry Number

77363-65-6

1 reference

https://commonchemistry.cas.org/detail?cas_rn=77363-65-6

9 April 2021

1 reference

5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-glucopyranosiduronic acid (English)

8 October 2016

2 references

Myricetin 3-O-glucuronide (English)

matched by identifier from

8 October 2016

Reaxys registry number

7401903

1 reference

myricetin 3-O-glucuronide (English)

8 October 2016

ChEBI ID

75807

mapping relation type

2 references

myricetin 3-O-glucuronide (English)

matched by identifier from

8 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H18O14/c22-6-3-7(23)11-10(4-6)33-17(5-1-8(24)12(26)9(25)2-5)18(13(11)27)34-21-16(30)14(28)15(29)19(35-21)20(31)32/h1-4,14-16,19,21-26,28-30H,(H,31,32)/t14-,15-,16+,19-,21+/m0/s1

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

CHEMBL458470 (English)

8 October 2016

1 reference

2 references

matched by identifier from