(Q5919049)

Gene Ontology release 2019-11-16

flavonol biosynthetic process

subject has role

product

1 reference

Gene Ontology release 2019-11-16

chemical structure

Flavonol.svg
242 × 189; 10 KB

0 references

mass

238.063 dalton

1 reference

3-Hydroxyflavone (English)

5 October 2016

chemical formula

C₁₅H₁₀O₃

1 reference

3-Hydroxyflavone (English)

5 October 2016

canonical SMILES

C1=CC=C(C=C1)C2=C(C(=O)C3=CC=CC=C3O2)O

1 reference

3-Hydroxyflavone (English)

5 October 2016

melting point

170.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Acacia acuminata

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia aneura

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia aulacocarpa

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia burrowii

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia cheelii

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia doratoxylon

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia excelsa

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia floribunda

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia harpophylla

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia holosericea

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia homalophylla

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia implexa

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia longifolia

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia melanoxylon

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia obtusifolia

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia oswaldii

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia pendula

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia pubifolia

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia pycnostachya

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia rigens

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia trineura

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia verniciflua

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia auriculiformis

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia maidenii

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia orites

1 reference

A phytochemical survey of the Australian species of Acacia

Chrysanthemum morifolium

1 reference

Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids

Trigonella foenum-graecum

2 references

Changes in the anti-nutritional factors of developing seeds and pod walls of fenugreek (Trigonella foenum graecum L.).

In vitro availability of iron from cereal meal with the addition of protein isolates and fenugreek leaves (Trigonella foenum-graecum).

Humulus lupulus

1 reference

Composition and In Vitro Effects of Cultivars of Humulus lupulus L. Hops on Cholinesterase Activity and Microbial Growth

Apium graveolens

1 reference

The impact of steam-blanching and dehydration on phenolic, organic acid composition, and total carotenoids in celery roots

Carica papaya

1 reference

HPLC-based activity profiling for antiplasmodial compounds in the traditional Indonesian medicinal plant Carica papaya L.

Arabidopsis thaliana

1 reference

Role of a chalcone isomerase-like protein in flavonoid biosynthesis in Arabidopsis thaliana

Momordica charantia

1 reference

Establishment of Momordica charantia hairy root cultures for the production of phenolic compounds and determination of their biological activities

Castanea sativa

1 reference

Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi

Ginkgo biloba

1 reference

Isolation, characterization, and function analysis of a flavonol synthase gene from Ginkgo biloba

Salvia officinalis

1 reference

Influence of sodium salicylate on rosmarinic acid, carnosol and carnosic acid accumulation by Salvia officinalis L. shoots grown in vitro

Broussonetia papyrifera

1 reference

Tyrosinase inhibitors from paper mulberry (Broussonetia papyrifera)

Psidium guajava

1 reference

The hypoglycemic effects of guava leaf (Psidium guajava L.) extract are associated with improving endothelial dysfunction in mice with diet-induced obesity

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Camellia sinensis

2 references

Characterization of catechins, theaflavins, and flavonols by leaf processing step in green and black teas (Camellia sinensis) using UPLC-DAD-QToF/MS

Purple foliage coloration in tea (Camellia sinensis L.) arises from activation of the R2R3-MYB transcription factor CsAN1.

Acacia omalophylla

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia retinodes

1 reference

A phytochemical survey of the Australian species of Acacia

Musa cavendishii

1 reference

Genome-wide Expression Analysis and Metabolite Profiling Elucidate Transcriptional Regulation of Flavonoid Biosynthesis and Modulation under Abiotic Stresses in Banana

Acacia concurrens

1 reference

A phytochemical survey of the Australian species of Acacia

Acacia binervia

1 reference

A phytochemical survey of the Australian species of Acacia

Eucalyptus globulus

1 reference

Low molecular weight polyphenols in leaves ofEucalyptus camaldulensis, E. globulusand E. rudis

Eucalyptus rudis

1 reference

Low molecular weight polyphenols in leaves ofEucalyptus camaldulensis, E. globulusand E. rudis

Eucalyptus camaldulensis

1 reference

Low molecular weight polyphenols in leaves ofEucalyptus camaldulensis, E. globulusand E. rudis

Commons category

Flavonol

0 references

Identifiers

InChI

InChI=1S/C15H10O3/c16-13-11-8-4-5-9-12(11)18-15(14(13)17)10-6-2-1-3-7-10/h1-9,17H

1 reference

3-Hydroxyflavone (English)

5 October 2016

2 references

3-Hydroxyflavone (English)

5 October 2016

ChEBI release 2020-09-01

2 references

flavonol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=577-85-5

9 April 2021

1 reference

3-Hydroxyflavone (English)

5 October 2016

2 references

3-Hydroxyflavone (English)

5 October 2016

Reaxys registry number

15789

1 reference

flavonol (English)

5 October 2016

454998

0 references

ChEBI ID

5078

mapping relation type

2 references

flavonol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H10O3/c16-13-11-8-4-5-9-12(11)18-15(14(13)17)10-6-2-1-3-7-10/h1-9,17H

1 reference

FLAVONOL (English)

5 October 2016

2 references

inferred from InChIKey

splash10-03dl-0920000000-3985dd52fbee952a4924

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

splash10-03di-0091000000-df578fdf47aa33cf9bdc

0 references

splash10-0059-0970000000-15b85abfede303ed7ad9

0 references

splash10-0a59-0590000000-264f4eaf4582ffd45cf0

0 references

splash10-000i-0090000000-bcacf0faaccb79b7fe26

0 references

splash10-0089-0930000000-daab83056ce346d57a1b

0 references

splash10-0089-1920000000-9eb3be9d053d3977fdf5

0 references

splash10-0089-1930000000-7c30acbf3bd077226a52

0 references

splash10-000i-0090000000-1f9d0b886f38ce8420c6

0 references

splash10-0a4i-0590000000-10f4c232ca8e92e78c04

0 references

splash10-0a4i-0590000000-f7f342168db7ea2b96c1

0 references

splash10-0a4i-0590000000-38e36b15d7b3ea71b0f6

0 references

splash10-0a4i-0690000000-2ccdb849b7e7472127ed

0 references

splash10-0a4i-0690000000-97a7698c6113b7a8c48e

0 references

splash10-000i-0090000000-cfa015b97699d9b8d3a9

0 references

splash10-000i-0090000000-372c492e8d989ae65894

0 references

splash10-0019-0490000000-028720cf2dae809285c2

0 references

splash10-001i-0910000000-637b7b8e665ded7f7238

0 references

splash10-000i-0790000000-da65563549c9dfb4d385

0 references

splash10-0002-1790000000-d7254b6d6e38adb8254b

0 references

splash10-0002-2790000000-fb06fe76861dbbc79bc2

0 references

HSDB ID

7572

1 reference

Hazardous Substances Data Bank

28 October 2019

3-HYDROXYFLAVONE (English)

10 May 2021

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

UNII

ZTG9LSS5QH

FLAVONOL (English)

ECHA Substance Infocard ID

5 October 2016

100.008.562

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.008.562

27 December 2018

imported from Wikimedia project

3-hydroxyflavone (English)

quotation

CAS no.: 577-85-5 (English)

Nikkaji ID

J1.628D

1 reference

Japanese Wikipedia

Human Metabolome Database ID

HMDB0031816

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00052681

2 references

based on heuristic

inferred from InChIKey

UNII

ZTG9LSS5QH

2 references

Global Substance Registration System

UNII

ZTG9LSS5QH

FLAVONOL (English)

5 October 2016

0 references

1 reference