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(Q748200)
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5,7-dihydroxyflavanone
pair of isomers
In more languages
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Statements
instance of
group of stereoisomers
0 references
subclass of
flavanone
1 reference
stated in
LIPID MAPS
chemical structure
Pinocembrin structure.svg
550 × 355; 23 KB
0 references
mass
256.073558864
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₅H₁₂O₄
2 references
imported from Wikimedia project
Italian Wikipedia
stated in
PubChem
canonical SMILES
O=C2c3c(OC(c1ccccc1)C2)cc(O)cc3O
1 reference
imported from Wikimedia project
English Wikipedia
found in taxon
Lychnophora ericoides
1 reference
stated in
Sesquiterpene lactones from Lychnophora ericoides.
Glycyrrhiza inflata
1 reference
stated in
Structural study of glabrisoflavone, a novel isoflavone fromGlycyrrhiza glabra L.
Vachellia pennatula
1 reference
stated in
Variation in chemical composition, antibacterial and antioxidant activity of fresh and dried Acacia leaf extracts
Boesenbergia
2 references
stated in
Medicinal foodstuffs. XXXIV. Structures of new prenylchalcones and prenylflavanones with TNF-alpha and aminopeptidase N inhibitory activities from Boesenbergia rotunda
stated in
Bioactive secondary metabolites from Boesenbergia pandurata of Myanmar and their preferential cytotoxicity against human pancreatic cancer PANC-1 cell line in nutrient-deprived medium.
Centaurea sonchifolia
1 reference
stated in
Biomimetic cyclization of cnicin to malacitanolide, a cytotoxic eudesmanolide from Centaurea malacitana
Uvaria lucida
2 references
stated in
New benzyldihydrochalcones from Uvaria chamae
stated in
Cytotoxic C-benzylated flavonoids from Uvaria chamae
Centaurea scoparia
1 reference
stated in
Biomimetic cyclization of cnicin to malacitanolide, a cytotoxic eudesmanolide from Centaurea malacitana
Piper callosum
1 reference
stated in
Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum
Populus
1 reference
stated in
Die lipophilen flavonoide des knospenöls von Populus nigra
Piper nigrum
1 reference
stated in
Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum
Betula alnoides
1 reference
stated in
Ermanin, ein neuer natürlicher Kämpferol-methyläther aus dem knospenexkret von Betula ermani
Helichrysum italicum
1 reference
stated in
Flavonoids and terpenoids from Helichrysum forskahlii
Anomianthus dulcis
2 references
stated in
New benzyldihydrochalcones from Uvaria chamae
stated in
Cytotoxic C-benzylated flavonoids from Uvaria chamae
Uvaria chamae
1 reference
stated in
New benzyldihydrochalcones from Uvaria chamae
Apis
1 reference
stated in
Effect of Pinocembrin Isolated from Mexican Brown Propolis on Diabetic Nephropathy
Centaurea seridis
1 reference
stated in
Biomimetic cyclization of cnicin to malacitanolide, a cytotoxic eudesmanolide from Centaurea malacitana
Populus deltoides
1 reference
stated in
Flavonoids of the buds of Populus balsamifera
Cassinia quinquefaria
1 reference
stated in
Exudate flavonoids from two australian asteraceae, Bracteantha viscosa and cassinia quinquefaria
Anomianthus
1 reference
stated in
Phenolic compounds from Anomianthus dulcis
Picea abies var. abies
2 references
stated in
Constituents of Pine Heartwood. XXV. Investigation of Forty-Eight Pinus Species by Paper Partition Chromatography.
stated in
Constituents of Pine Heartwood. XV. The Heartwood of Pinus excelsa Wall..
Pinus contorta var. latifolia
3 references
stated in
Constituents of Pine Heartwood. XXV. Investigation of Forty-Eight Pinus Species by Paper Partition Chromatography.
stated in
Constituents of Pine Heartwood. XI. The Heartwood of Pinus radiata D. Don.
stated in
Constituents of Pine Heartwood. X. The Heartwood of Pinus contorta var. latifolia S. Wats.
Adenostoma sparsifolium
1 reference
stated in
Flavonoids from the leaf resin of Adenostoma sparsifolium
Pinus montana
1 reference
stated in
Constituents of Pine Heartwood. IX. The Heartwood of Pinus montana Mill.
Pinus contorta
1 reference
stated in
Constituents of Pine Heartwood. X. The Heartwood of Pinus contorta var. latifolia S. Wats.
Pinus jeffreyi
1 reference
stated in
Constituents of Pine Heartwood. XIII. The Heartwood of Pinus Jeffreyi Balf.
Pinus ponderosa
1 reference
stated in
Constituents of Pine Heartwood. XII. The Heartwood of Pinus ponderosa Dougl.
Pinus virginiana
1 reference
stated in
Constituents of Pine Heartwood. XVI. The Heartwood of Pinus virginiana Mill..
Ericameria nauseosa
1 reference
stated in
Flavonoids from Ericameria nauseosa inhibiting PI3K/AKT pathway in human melanoma cells
Zuccagnia punctata
1 reference
stated in
Antifungal chalcones and new caffeic acid esters from Zuccagnia punctata acting against soybean infecting fungi.
Pinalia pandurata
1 reference
stated in
Constituents of Boesenbergia pandurata (syn. Kaempferia pandurata): Isolation, Crystal Structure and Synthesis of (±)-Boesenbergin A
Mangifera indica
1 reference
stated in
Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity
Stellaria dichotoma
1 reference
stated in
Bioactive constituents from Chinese natural medicines. XIV. New glycosides of beta-carboline-type alkaloid, neolignan, and phenylpropanoid from Stellaria dichotoma L. var. lanceolata and their antiallergic activities.
Boesenbergia rotunda
1 reference
stated in
Constituents of Boesenbergia pandurata (syn. Kaempferia pandurata): Isolation, Crystal Structure and Synthesis of (±)-Boesenbergin A
Pinus mugo
1 reference
stated in
Constituents of Pine Heartwood. IX. The Heartwood of Pinus montana Mill.
Pinus pungens
1 reference
stated in
Constituents of Pine Heartwood. IX. The Heartwood of Pinus montana Mill.
Identifiers
InChI
InChI=1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2
1 reference
stated in
PubChem
InChIKey
URFCJEUYXNAHFI-UHFFFAOYSA-N
1 reference
stated in
PubChem
ChemSpider ID
208593
1 reference
imported from Wikimedia project
English Wikipedia
PubChem CID
238782
1 reference
imported from Wikimedia project
English Wikipedia
ChEMBL ID
CHEMBL399910
1 reference
imported from Wikimedia project
English Wikipedia
SureChEMBL ID
SCHEMBL291899
1 reference
based on heuristic
inferred from InChIKey
UniChem compound ID
691548
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-Fac_Eng_Univ_Tokyo-JP000718
0 references
MSBNK-Washington_State_Univ-BML00869
0 references
MSBNK-Washington_State_Univ-BML00878
0 references
MSBNK-Washington_State_Univ-BML00887
0 references
MSBNK-Washington_State_Univ-BML00892
0 references
MSBNK-Washington_State_Univ-BML00897
0 references
MSBNK-Washington_State_Univ-BML00902
0 references
MSBNK-Washington_State_Univ-BML81965
0 references
MSBNK-Washington_State_Univ-BML81966
0 references
MSBNK-Washington_State_Univ-BML81967
0 references
MSBNK-Washington_State_Univ-BML81968
0 references
SPLASH
splash10-0a4i-0490000000-e3e0fd288f81b7d8a9f6
0 references
splash10-0udi-0900000000-bb65e58e45d6926a4d0e
0 references
splash10-0udi-0900000000-405d5e70eb1870fb79b7
0 references
splash10-0a4i-0090000000-e7a2d42e43fa0b871d58
0 references
splash10-0a4i-0490000000-db48745a3d543c14c6fc
0 references
splash10-0pi0-0900000000-31c7469fd05b2dfa0d26
0 references
splash10-0a4i-0090000000-7c3a74cf7e01436ee64a
0 references
splash10-0a4i-0090000000-de17696c7369872e0a2a
0 references
splash10-0a4i-0090000000-84235fc0e6a9b64a53ff
0 references
splash10-03di-0590000000-694b7335d1677c72efb9
0 references
splash10-004i-0890000000-123a4c1e576644198225
0 references
splash10-0udi-0920000000-51d135533a4a8f649cba
0 references
splash10-0sra-0990000000-2ff19c1dd1db18d885d7
0 references
KNApSAcK ID
C00000992
0 references
C00062693
1 reference
based on heuristic
inferred from InChIKey
Probes And Drugs ID
PD056515
0 references
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