isoquercitrin (Q27103621)

Isoquercitroside (English)

5 October 2016

2 references

inferred from InChIKey

3-[(2S,3R,4S,5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

inferred from InChI

2 references

inferred from InChIKey

inferred from InChI

chemical formula

C₂₁H₂₀O₁₂

1 reference

Isoquercitroside (English)

19 November 2016

canonical SMILES

C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O

1 reference

Isoquercitroside (English)

19 November 2016

isomeric SMILES

C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@H](O4)[C@@H](CO)O)O)O)O)O

1 reference

Isoquercitroside (English)

19 November 2016

found in taxon

Reynoutria sachalinensis

1 reference

A flavonoid glycoside from the leaves ofPolygonum sachalinense (II)

Dysphania botrys

1 reference

Flavonoids of Chenopodium botrys

Trifolium repens

1 reference

Clover root exudate contains a particulate form of the lectin, trifoliin A, which binds Rhizobium trifolii

Lonicera japonica

1 reference

Identification and quantification of 32 bioactive compounds in Lonicera species by high performance liquid chromatography coupled with time-of-flight mass spectrometry

Acmella ciliata

1 reference

New phenolic compounds of Acmella ciliata

Astragalus bornmuellerianus

1 reference

Flavonoids ofAstragalus bornmüllerianus

Astragalus captiosus

1 reference

Flavonoids ofAstragalus captiosus

Camellia japonica

1 reference

Camellianoside, a novel antioxidant glycoside from the leaves of Camellia japonica

Camellia sinensis

1 reference

Flavonoids ofCamellia sinensis

Caragana spinosa

1 reference

Chemical investigation of Caragana spinosa runners

Volutaria lippii

1 reference

Secondary metabolites from Centaurea lippii

Euphorbia marschalliana

1 reference

Flavonoids ofEuphorbia armena

Euphorbia smirnovii

1 reference

Flavonoids ofEuphorbia armena

Globularia bisnagarica

1 reference

ChemInform Abstract: Flavonoid, Phenylethanoid and Iridoid Glycosides from Globularia aphyllanthes

Hedysarum coronarium

1 reference

Condensed tannins and flavonoids from the forage legume sulla (Hedysarum coronarium).

Hypericum brasiliense

1 reference

Antibacterial phloroglucinols and flavonoids from Hypericum brasiliense

Hypericum elegans

1 reference

Benzophenone O-glycosides from Hypericum elegans

Hypericum perforatum

2 references

High-Performance Liquid Chromatography On-Line Coupled to High-Field NMR and Mass Spectrometry for Structure Elucidation of Constituents ofHypericum perforatumL.

Investigations on the in vivo wound healing potential of Hypericum perforatum L.

Lagerstroemia speciosa

1 reference

Active compounds from Lagerstroemia speciosa, insulin-like glucose uptake-stimulatory/inhibitory and adipocyte differentiation-inhibitory activities in 3T3-L1 cells.

Marrubium velutinum

1 reference

Acylated flavonoid and phenylethanoid glycosides from Marrubium velutinum

Nelumbo nucifera

1 reference

Constituents from the leaves of Nelumbo nucifera stimulate lipolysis in the white adipose tissue of mice

Phaseolus vulgaris

1 reference

Flavonoids ofPhaseolus vulgaris

Phoenix loureiroi var. loureiroi

1 reference

Neural cell protective compounds isolated from Phoenix hanceana var. formosana.

Phyllanthus virgatus

1 reference

Tannins, flavonol sulfonates, and a norlignan from phyllanthus virgatus

Salix caprea

1 reference

Flavonoids from Salix caprea

Salix denticulata

1 reference

Isolation and characterization of a new flavone diglucoside from Salix denticulata

Sorbus aria

1 reference

Activity-guided isolation and identification of free radical-scavenging components from various leaf extracts of Sorbus aria (L.) Crantz

Tripodanthus acutifolius

1 reference

Free radical scavenging activities and inhibition of inflammatory enzymes of phenolics isolated from Tripodanthus acutifolius

Viburnum tinus

1 reference

Phytochemical constituents and hepatoprotective activity of Viburnum tinus

Vicia sativa

1 reference

Coumarins ofVicia sativa

Warburgia ugandensis

1 reference

Flavonol glycosides of Warburgia ugandensis leaves

Epilobium dodonaei

1 reference

Compounds fromEpilobium angustifoliumInhibit the Specific Metallopeptidases ACE, NEP and APN

Aria edulis

1 reference

Activity-guided isolation and identification of free radical-scavenging components from various leaf extracts of Sorbus aria (L.) Crantz

Chamaenerion dodonaei

1 reference

Compounds fromEpilobium angustifoliumInhibit the Specific Metallopeptidases ACE, NEP and APN

Epilobium prantlii

1 reference

Compounds fromEpilobium angustifoliumInhibit the Specific Metallopeptidases ACE, NEP and APN

Sulla coronaria

1 reference

Condensed tannins and flavonoids from the forage legume sulla (Hedysarum coronarium).

Chenopodium botrys

1 reference

Flavonoids of Chenopodium botrys

Matteuccia struthiopteris

1 reference

Changes during gametophyte development in Matteuccia struthiopteris from the cinnamate to the chalcone synthase pathway

Identifiers

InChI

InChI=1S/C21H20O12/c22-6-12(27)19-16(29)17(30)21(32-19)33-20-15(28)14-11(26)4-8(23)5-13(14)31-18(20)7-1-2-9(24)10(25)3-7/h1-5,12,16-17,19,21-27,29-30H,6H2/t12-,16-,17-,19-,21+/m1/s1

1 reference

Isoquercitroside (English)

19 November 2016

2 references

Isoquercitroside (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

21637-25-2

2 references

Global Substance Registration System

isoquercitrin (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=21637-25-2

9 April 2021

1 reference

3,3',4',5,7-Pentahydroxyflavone 3-b-D-glucofuranoside (English)

19 November 2016

2 references

Isoquercitroside (English)

19 November 2016

Reaxys registry number

1444784

1 reference

quercetin 3-O-beta-D-glucofuranoside (English)

5 October 2016

ChEBI ID

28299

mapping relation type

2 references

quercetin 3-O-beta-D-glucofuranoside (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H20O12/c22-6-12(27)19-16(29)17(30)21(32-19)33-20-15(28)14-11(26)4-8(23)5-13(14)31-18(20)7-1-2-9(24)10(25)3-7/h1-5,12,16-17,19,21-27,29-30H,6H2/t12-,16-,17-,19-,21+/m1/s1

SureChEMBL ID

SCHEMBL24608

2 references

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

DTXCID101334095

0 references

EC number

244-488-5

1 reference

Global Substance Registration System

isoquercitrin (English)

ECHA Substance Infocard ID

19 November 2016

100.040.429

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.040.429

27 December 2018

2-(3,4-dihydroxyphenyl)-3-(β-D-glucofuranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one (English)

quotation

CAS no.: 21637-25-2 (English)

1 reference

28 December 2019

ISOQUERCITRIN (English)

quotation

CAS no.: 21637-25-2 (English)

DrugBank ID

DB16403

1 reference

2 references

Global Substance Registration System

isoquercitrin (English)

19 November 2016