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(Q104972046)
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English
2,3-dihydroquercetin
group of stereoisomers with the chemical formula C₁₅H₁₂O₇
In more languages
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Statements
instance of
group of stereoisomers
0 references
subclass of
flavanone
1 reference
inferred from
flavanone
mass
304.058302724
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₅H₁₂O₇
0 references
canonical SMILES
O=C1C=2C(O)=CC(O)=CC2OC(C3=CC=C(O)C(O)=C3)C1O
0 references
found in taxon
Acacia adunca
4 references
stated in
α-Amylase and lipase inhibitory activity and structural characterization of acacia bark proanthocyanidins
stated in
Isolation of [4-O-4]-linked biflavanoids from Acacia melanoxylon: first examples of a new class of single ether-linked proanthocyanidin dimers
stated in
A new flavan-3,4-diol from Acacia auriculiformis by paper ionophoresis
stated in
Metabolites from the purple heartwood of Mimosoideae. Part 2. Acacia carnei maiden: isolation, synthesis, and reactions of crombeone
Excoecaria acerifolia
1 reference
stated in
Chemical constituents of Excoecaria acerifolia and their bioactivities
Prunus lycioides
1 reference
stated in
Chiral flavanones from Amygdalus lycioides Spach: structural elucidation and identification of TNFalpha inhibitors by bioactivity-guided fractionation
Bidens parviflora
1 reference
stated in
Flavonoids and a new polyacetylene from Bidens parviflora Willd.
Fagus grandifolia
1 reference
stated in
The extractives of New Zealand Nothofagus species
Eucalyptus melliodora
1 reference
stated in
Polyphenols and the Distribution of Arboreal, Folivorous Marsupials in Eucalyptus Forests of Australia
Artemisia incanescens
1 reference
stated in
Guaiane dimers and germacranolide from Artemisia caruifolia
Thymus quinquecostatus
1 reference
stated in
Isolation and structure elucidation of radical scavengers from Thymus vulgaris leaves.
Artemisia assoana
1 reference
stated in
Guaiane dimers and germacranolide from Artemisia caruifolia
Juglans nigra
1 reference
stated in
Inhibition of human immunodeficiency virus type 1 reverse transcriptase and ribonuclease H activities by constituents of Juglans mandshurica
Eucalyptus apodophylla
1 reference
stated in
Polyphenols and the Distribution of Arboreal, Folivorous Marsupials in Eucalyptus Forests of Australia
Thymus piperella
1 reference
stated in
Isolation and structure elucidation of radical scavengers from Thymus vulgaris leaves.
Kadsura
1 reference
stated in
Compounds from Kadsura heteroclita and related anti-HIV activity
Polygala reinii
1 reference
stated in
Xanthones from Polygala caudata
Artemisia absinthium
1 reference
stated in
Guaiane dimers and germacranolide from Artemisia caruifolia
Nothofagus
1 reference
stated in
The extractives of New Zealand Nothofagus species
Garcinia brasiliensis
1 reference
stated in
Antibacterial and brine shrimp lethality tests of biflavonoids and derivatives of Rheedia gardneriana
Peltophorum dasyrachis
1 reference
stated in
Tyrosinase inhibitory constituents from the bark of Peltophorum dasyrachis (yellow batai)
Acacia carneorum
3 references
stated in
α-Amylase and lipase inhibitory activity and structural characterization of acacia bark proanthocyanidins
stated in
Isolation of [4-O-4]-linked biflavanoids from Acacia melanoxylon: first examples of a new class of single ether-linked proanthocyanidin dimers
stated in
A new flavan-3,4-diol from Acacia auriculiformis by paper ionophoresis
Pinus sylvestris
1 reference
stated in
Phenolic extractives from the bark of Pinus sylvestris L. and their effects on inflammatory mediators nitric oxide and prostaglandin E2.
Rhamnus pallasii
1 reference
stated in
Polyphenolic metabolites of Rhamnus disperma
Acacia mearnsii
3 references
stated in
Isolation of [4-O-4]-linked biflavanoids from Acacia melanoxylon: first examples of a new class of single ether-linked proanthocyanidin dimers
stated in
A new flavan-3,4-diol from Acacia auriculiformis by paper ionophoresis
stated in
Metabolites from the purple heartwood of Mimosoideae. Part 2. Acacia carnei maiden: isolation, synthesis, and reactions of crombeone
Coast Douglas-fir
1 reference
stated in
Pseudotsuganol, a biphenyl-linked pinoresinol–dihydroquercetin from douglas-fir bark: isolation of the first true flavonolignan
Cedrus deodara
1 reference
stated in
Dihydroflavonols from Cedrus deodara
Rhododendron dauricum
1 reference
stated in
Chromatographic and electrophoretic methods for pharmaceutically active compounds in Rhododendron dauricum
Sarcandra glabra
1 reference
stated in
Chemical profiling of bioactive constituents in Sarcandra glabra and its preparations using ultra-high-pressure liquid chromatography coupled with LTQ Orbitrap mass spectrometry
Glycyrrhiza uralensis
1 reference
stated in
Identification and Enrichment of α-Glucosidase-Inhibiting Dihydrostilbene and Flavonoids from Glycyrrhiza uralensis Leaves.
Pulicaria canariensis
2 references
stated in
Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities
stated in
Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities
Distylium racemosum
1 reference
stated in
On The Chemical Constituents Of The Heart Wood Of Distylium Racemosum S. ET Z. (First Report)
Artemisia alba
1 reference
stated in
Guaiane dimers and germacranolide from Artemisia caruifolia
Artemisia pedemontana
1 reference
stated in
Guaiane dimers and germacranolide from Artemisia caruifolia
Eucalyptus maidenii
1 reference
stated in
Phenolic compounds from the branches of Eucalyptus maideni
Persicaria hydropiper
1 reference
stated in
Inhibitory compound of tyrosinase activity from the sprout of Polygonum hydropiper L. (Benitade).
Prunus serrulata
1 reference
stated in
Padmatin, a new component of the heartwood of Prunus puddum
Identifiers
InChI
InChI=1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H
0 references
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
0 references
PubChem CID
471
1 reference
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
ChEBI ID
38747
mapping relation type
exact match
1 reference
stated in
ChEBI release 2021-03-01
UniChem compound ID
588112
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-RIKEN-PR309311
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_NPDepo-CB000303
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_NPDepo-NGA03057
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_NPDepo-NGA03058
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_NPDepo-NGA03059
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_NPDepo-NGA03060
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_ReSpect-PS069601
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_ReSpect-PS069607
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_ReSpect-PS069609
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN_ReSpect-PS069608
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML01255
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML01273
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML01276
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML01279
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML81120
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML81122
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML81121
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-Washington_State_Univ-BML81123
1 reference
InChIKey
CXQWRCVTCMQVQX-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
Human Metabolome Database ID
HMDB0242509
1 reference
based on heuristic
inferred from InChIKey
KNApSAcK ID
C00060794
1 reference
based on heuristic
inferred from InChIKey
Probes And Drugs ID
PD014975
0 references
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