(Q25098661)

naringenin chalcone (English)

4 October 2016

chemical formula

C₁₅H₁₂O₅

1 reference

naringenin chalcone (English)

4 October 2016

canonical SMILES

C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2O)O)O)O

1 reference

naringenin chalcone (English)

4 October 2016

isomeric SMILES

C1=CC(=CC=C1/C=C/C(=O)C2=C(C=C(C=C2O)O)O)O

1 reference

Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate

naringenin chalcone (English)

4 October 2016

1 reference

Populus tremula

1 reference

Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate

Populus tremuloides

1 reference

Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate

Populus tristis

1 reference

Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS

Populus koreana

1 reference

Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS

Populus suaveolens

1 reference

Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS

Populus maximowiczii

1 reference

Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS

Populus cathayana

1 reference

Analysis of Phenolics of Bud Exudates of Populus cathayana and Populus szechuanica by GC-MS

Populus szechuanica

1 reference

Analysis of Phenolics of Bud Exudates of Populus cathayana and Populus szechuanica by GC-MS

Arabidopsis thaliana

1 reference

The Arabidopsis TDS4 gene encodes leucoanthocyanidin dioxygenase (LDOX) and is essential for proanthocyanidin synthesis and vacuole development.

Ipomoea nil

1 reference

Flavonoids in the acyanic flowers of Pharbitis nil

Matthiola incana

1 reference

Relationship between Flower Development, Anthocyanin Accumulation and Activity o f Enzymes Involved in Flavonoid Biosynthesis in Matthiola incana R. Br

Salvia leucantha

1 reference

Salvigenane and isosalvipuberulan diterpenoids from Salvia leucantha

Salvia xalapensis

2 references

Unsaturated diterpenoids with a novel carbocyclic skeleton from Salvia xalapensis

Unsaturated diterpenoids with a novel carbocyclic skeleton from Salvia xalapensis

Humulus lupulus

1 reference

Phytochemical and morphological characterization of hop (Humulus lupulus L.) cones over five developmental stages using high performance liquid chromatography coupled to time-of-flight mass spectrometry, ultrahigh performance liquid chromatography p

Punica granatum

1 reference

A "White" Anthocyanin-less Pomegranate (Punica granatum L.) Caused by an Insertion in the Coding Region of the Leucoanthocyanidin Dioxygenase (LDOX; ANS) Gene

asparagus

1 reference

Transcriptome analysis of Asparagus officinalis reveals genes involved in the biosynthesis of rutin and protodioscin

Momordica charantia

1 reference

Identification and Characterization of Phenylpropanoid Biosynthetic Genes and Their Accumulation in Bitter Melon (Momordica charantia).

Magnolia denudata

1 reference

Analysis of Metabolites in White Flowers of Magnolia Denudata Desr. and Violet Flowers of Magnolia Liliiflora Desr.

Magnolia liliiflora

1 reference

Analysis of Metabolites in White Flowers of Magnolia Denudata Desr. and Violet Flowers of Magnolia Liliiflora Desr.

Great yellow gentian

1 reference

Differential accumulation of pelargonidin glycosides in petals at three different developmental stages of the orange-flowered gentian (Gentiana lutea L. var. aurantiaca)

pea

1 reference

Effect of germination time on antioxidative activity and composition of yellow pea soluble free and polar soluble bound phenolic compounds

Streptomyces venezuelae

2 references

Enhanced flavonoid production in Streptomyces venezuelae via metabolic engineering

Engineering of plant-specific phenylpropanoids biosynthesis in Streptomyces venezuelae.

Populus trichocarpa

1 reference

Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS

Ginkgo biloba

1 reference

De novo transcriptome analysis revealed genes involved in flavonoid biosynthesis, transport and regulation in Ginkgo biloba

Identifiers

InChI

InChI=1S/C15H12O5/c16-10-4-1-9(2-5-10)3-6-12(18)15-13(19)7-11(17)8-14(15)20/h1-8,16-17,19-20H/b6-3+

1 reference

naringenin chalcone (English)

YQHMWTPYORBCMF-ZZXKWVIFSA-N

4 October 2016

InChIKey

2 references

naringenin chalcone (English)

4 October 2016

ChEBI release 2020-09-01

1 reference

2',4,4',6'-tetrahydroxychalcone (English)

4 October 2016

1 reference

naringenin chalcone (English)

4 October 2016

1 reference

naringenin chalcone (English)

4 October 2016

Reaxys registry number

2335724

1 reference

2',4,4',6'-tetrahydroxychalcone (English)

4 October 2016

ChEBI ID

15413

mapping relation type

2 references

2',4,4',6'-tetrahydroxychalcone (English)

4 October 2016

ChEBI release 2019-10-02

1 reference

splash10-0udj-0920000000-1bfd55f600a901a79c87

4,2',4',6'-TETRAHYDROXYCHALCONE (English)

4 October 2016

1 reference

MassBank accession ID

MSBNK-IPB_Halle-PB000126

0 references

MSBNK-IPB_Halle-PB000127

0 references

MSBNK-IPB_Halle-PB000128

0 references

MSBNK-IPB_Halle-PB000129

0 references

MSBNK-IPB_Halle-PB002405

0 references

MSBNK-IPB_Halle-PB002406

0 references

MSBNK-IPB_Halle-PB002407

0 references

MSBNK-IPB_Halle-PB002408

0 references

SPLASH

0 references

splash10-0udi-0900000000-79afec38b3dde07593f3

0 references

splash10-0gbc-9700000000-ed15b50aa1d66f06bf42

0 references

splash10-00di-0190000000-f40a3d639173b6ae573e

0 references

splash10-0udi-0910000000-afe3bb20e73181050052

0 references

splash10-014i-2900000000-37be5bc5a9f1bc38d302

0 references

splash10-014i-7900000000-42ef7b65ce430e844b49

0 references

1 reference

Human Metabolome Database ID

HMDB0029631

1 reference

based on heuristic

inferred from InChIKey

2 references

2',4,4',6'-tetrahydroxychalcone (English)

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

4 October 2016

based on heuristic

inferred from InChIKey

C00052701

1 reference

based on heuristic

inferred from InChIKey

0 references

0 references

1 reference