5,7-dihydroxyflavanone (Q748200)

pair of isomers

Language	Label	Description	Also known as
English	5,7-dihydroxyflavanone	pair of isomers

Statements

instance of

group of stereoisomers

0 references

1 reference

Pinocembrin structure.svg
550 × 355; 23 KB

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mass

256.073558864 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₁₅H₁₂O₄

2 references

imported from Wikimedia project

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

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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

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

1 reference

MassBank accession ID

MSBNK-Fac_Eng_Univ_Tokyo-JP000718

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MSBNK-Washington_State_Univ-BML00869

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MSBNK-Washington_State_Univ-BML00878

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MSBNK-Washington_State_Univ-BML00887

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MSBNK-Washington_State_Univ-BML00892

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MSBNK-Washington_State_Univ-BML00897

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MSBNK-Washington_State_Univ-BML00902

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MSBNK-Washington_State_Univ-BML81965

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MSBNK-Washington_State_Univ-BML81966

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MSBNK-Washington_State_Univ-BML81967

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MSBNK-Washington_State_Univ-BML81968

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SPLASH

splash10-0a4i-0490000000-e3e0fd288f81b7d8a9f6

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splash10-0udi-0900000000-bb65e58e45d6926a4d0e

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splash10-0udi-0900000000-405d5e70eb1870fb79b7

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splash10-0a4i-0090000000-e7a2d42e43fa0b871d58

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splash10-0a4i-0490000000-db48745a3d543c14c6fc

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splash10-0pi0-0900000000-31c7469fd05b2dfa0d26

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splash10-0a4i-0090000000-7c3a74cf7e01436ee64a

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splash10-0a4i-0090000000-de17696c7369872e0a2a

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splash10-0a4i-0090000000-84235fc0e6a9b64a53ff

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splash10-03di-0590000000-694b7335d1677c72efb9

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splash10-004i-0890000000-123a4c1e576644198225

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splash10-0udi-0920000000-51d135533a4a8f649cba

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splash10-0sra-0990000000-2ff19c1dd1db18d885d7

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0 references

1 reference

inferred from InChIKey

Probes And Drugs ID

PD056515

0 references

5,7-dihydroxyflavanone (Q748200)

Statements

Identifiers

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5,7-dihydroxyflavanone (Q748200)

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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