(Q2402963)

Nobiletin (English)

5 October 2016

C₂₁H₂₂O₈

1 reference

Nobiletin (English)

5 October 2016

COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Nobiletin (English)

5 October 2016

2 references

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

Citrus flavicarpa

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus intermedia

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus hassaku

3 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

Citrus otachibana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus obovoidea

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus sulcata

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus ×iyo

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus ujukitsu

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus aurea

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus shunkokan

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus hanaju

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus sudachi

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus nippokoreana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus keraji

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus oto

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus tachibana

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus erythrosa

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Cherry Orange

4 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Citrus depressa

3 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Nobiletin, a citrus flavonoid with neurotrophic action, augments protein kinase A-mediated phosphorylation of the AMPA receptor subunit, GluR1, and the postsynaptic receptor response to glutamate in murine hippocampus.

Citrus leiocarpa

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus madurensis

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Ageratum conyzoides

3 references

Methoxyflavones from Ageratum conyzoides

Polyoxygenated flavones from Ageratum conyzoides

Polyoxygenated flavones from Ageratum conyzoides

Ozothamnus lycopodioides

3 references

A new oxyprenyl coumarin and highly methylated flavones from the exudate of Ozothamnus lycopodioides (Asteraceae)

A new oxyprenyl coumarin and highly methylated flavones from the exudate of Ozothamnus lycopodioides (Asteraceae)

New Constituents of the Leaf and Stem Exudate of Ozothamnus hookeri (Asteraceae)

Viburnum tinus

2 references

Phytochemical constituents and hepatoprotective activity of Viburnum tinus

Phytochemical constituents and hepatoprotective activity of Viburnum tinus

Citrus pseudoparadisi

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus

4 references

Nobiletin as a tyrosinase inhibitor from the peel of Citrus fruit

Anti-tumour effects of nobiletin, a citrus flavonoid, on gastric cancer include: antiproliferative effects, induction of apoptosis and cell cycle deregulation

Interactive effects of polymethoxy flavones from Citrus on cell growth inhibition in human neuroblastoma SH-SY5Y cells

Tyrosinase inhibitory effects and inhibition mechanisms of nobiletin and hesperidin from citrus peel crude extracts.

Juncus effusus

2 references

Two p-coumaroyl glycerides from Juncus effusus

Two p-coumaroyl glycerides from Juncus effusus

Tripterygium wilfordii

1 reference

Chemical Constituents from the Root of Tripterygium wilfordii

Blumea glomerata

1 reference

Isolation of austroinulin possessing cell cycle inhibition activity from Blumea glomerata and revision of its absolute configuration

Eupatorium leucolepis

1 reference

Flavones from Eupatorium leucolepis

Oxalis pes-caprae

1 reference

Phytotoxic aromatic constituents of Oxalis pes-caprae

Croton caudatus

1 reference

Flavonoids from the stems of Croton caudatus Geisel. var. tomentosus Hook.

Sorbus pallescens

1 reference

The flavonoid nobiletin inhibits tumor growth and angiogenesis of ovarian cancers via the Akt pathway

Griffitharia pallescens

1 reference

The flavonoid nobiletin inhibits tumor growth and angiogenesis of ovarian cancers via the Akt pathway

Citrus grandis

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus tankan

2 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

The Chemical Constituents of the Peel of Citrus Tankan Hayata

Citrus unshiu

5 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Anti-allergic components from the peels of Citrus unshiu

Polymethoxylated flavonoids from the peel of Unshiu mandarin fruit

Pharmacological Study on Citrus Fruits. II. Anti-allergic Effect of Fruit of Citrus unshiu MARKOVICH (2). On Flavonoid Components

Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong

Citrus nobilis

1 reference

Quantitation of flavonoid constituents in citrus fruits

Citrus × paradisi

4 references

Variance of common flavonoids by brand of grapefruit juice

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Simultaneous separation of flavanone glycosides and polymethoxylated flavones in citrus juices using liquid chromatography

Use of an online extraction liquid chromatography quadrupole time-of-flight tandem mass spectrometry method for the characterization of polyphenols in Citrus paradisi cv. Changshanhuyu peel

Paepalanthus polyanthus

1 reference

6-Methoxyquercetin-3-O-(6″-E-feruloyl)-β-d-glucopyranoside from Paepalanthus polyanthus (Eriocaulaceae)

Capsicum annuum

1 reference

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

Citrus × deliciosa

19 references

The Chemical Constituents of the Peel of Citrus Tankan Hayata

Pharmacological Study on Citrus Fruits. II. Anti-allergic Effect of Fruit of Citrus unshiu MARKOVICH (2). On Flavonoid Components

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Polymethoxylated flavonoids from the peel of Unshiu mandarin fruit

Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong

Anti-allergic components from the peels of Citrus unshiu

Quantitation of flavonoid constituents in citrus fruits

Nobiletin, a citrus flavonoid with neurotrophic action, augments protein kinase A-mediated phosphorylation of the AMPA receptor subunit, GluR1, and the postsynaptic receptor response to glutamate in murine hippocampus.

Citrus Polymethoxylated Flavones Can Confer Resistance againstPhytophthora citrophthora,Penicillium digitatum, andGeotrichumSpecies

Studies on the differentiation inducers of myeloid leukemic cells from Citrus species.

Isolation and Identification of New Polymethoxyflavonoids from Dancy Tangerine Leaves

Isolation of anti-leukemia compounds from Citrus reticulata

Antibacterial activity of Citrus reticulata peel extracts

The methoxyflavones in Citrus reticulata Blanco cv. ponkan and their antiproliferative activity against cancer cells

Studies on the constituents of useful plants. V. Multisubstituted flavones in the fruit peel of Citrus reticulata and their examination by gas-liquid chromatography.

Two New Polymethoxylated Flavones, a Class of Compounds with Potential Anticancer Activity, Isolated from Cold Pressed Dancy Tangerine Peel Oil Solids

Kumquat

5 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Methoxylated flavones of Fortunella japonica

pomelo

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Blumea fistulosa

1 reference

Isolation of austroinulin possessing cell cycle inhibition activity from Blumea glomerata and revision of its absolute configuration

Citrus myrtifolia

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Plenodomus tracheiphilus

1 reference

Fungistatic flavones in the leaves of citrus species resistant and susceptible to deuterophoma tracheiphila

Barbados nut

1 reference

Chemical constituents from leaves of Jatropha curcas

mandarin orange

19 references

The Chemical Constituents of the Peel of Citrus Tankan Hayata

Pharmacological Study on Citrus Fruits. II. Anti-allergic Effect of Fruit of Citrus unshiu MARKOVICH (2). On Flavonoid Components

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Studies on the constituents of useful plants. V. Multisubstituted flavones in the fruit peel of Citrus reticulata and their examination by gas-liquid chromatography.

Anti-allergic components from the peels of Citrus unshiu

Isolation of anti-leukemia compounds from Citrus reticulata

The methoxyflavones in Citrus reticulata Blanco cv. ponkan and their antiproliferative activity against cancer cells

Isolation and Identification of New Polymethoxyflavonoids from Dancy Tangerine Leaves

Antibacterial activity of Citrus reticulata peel extracts

Studies on the differentiation inducers of myeloid leukemic cells from Citrus species.

Two New Polymethoxylated Flavones, a Class of Compounds with Potential Anticancer Activity, Isolated from Cold Pressed Dancy Tangerine Peel Oil Solids

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Polymethoxylated flavonoids from the peel of Unshiu mandarin fruit

Citrus Polymethoxylated Flavones Can Confer Resistance againstPhytophthora citrophthora,Penicillium digitatum, andGeotrichumSpecies

Quantitation of flavonoid constituents in citrus fruits

Nobiletin, a citrus flavonoid with neurotrophic action, augments protein kinase A-mediated phosphorylation of the AMPA receptor subunit, GluR1, and the postsynaptic receptor response to glutamate in murine hippocampus.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong

Citrus japonica

5 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Methoxylated flavones of Fortunella japonica

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

physically interacts with

taste receptor type 2

subject has role

agonist

1 reference

Bitter substances from plants used in traditional Chinese medicine exert biased activation of human bitter taste receptors

1 reference

1 reference

Medical Subject Headings

MeSH descriptor ID

C008661

InChI=1S/C21H22O8/c1-23-13-8-7-11(9-15(13)24-2)14-10-12(22)16-17(25-3)19(26-4)21(28-6)20(27-5)18(16)29-14/h7-10H,1-6H3

15 March 2018

Identifiers

InChI

1 reference

Nobiletin (English)

5 October 2016

2 references

Nobiletin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

nobiletin (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=478-01-3

9 April 2021

1 reference

Nobiletin (English)

5 October 2016

2 references

English

title

Nobiletin (English)

5 October 2016

Reaxys registry number

360887

1 reference

nobiletin (English)

5 October 2016

mapping relation type

2 references

English

title

nobiletin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H22O8/c1-23-13-8-7-11(9-15(13)24-2)14-10-12(22)16-17(25-3)19(26-4)21(28-6)20(27-5)18(16)29-14/h7-10H,1-6H3

1 reference

NOBILETIN (English)

5 October 2016

2 references

inferred from InChIKey

splash10-0079-0009000000-56a6a884637d33258efe

1 reference

0 references

splash10-0079-0009000000-48e1c6b0ffa49a0b6e4d

0 references

splash10-00dr-0009000000-f52ca9b39e356ac4b12b

0 references

splash10-0079-0009000000-e6c60c19f841c799eced

0 references

splash10-0079-0009000000-e3adbaeb16824184d38d

0 references

splash10-0079-0009000000-23b9b2722326c27392ba

0 references

splash10-0udi-0003900000-ac65f1ec47828763a141

0 references

splash10-0uki-0009600000-0083269e95dcfc2ee6e7

0 references

splash10-0079-0009000000-0f9ba491f594df619782

0 references

DSSTox substance ID

DTXSID30197275

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

Medical Subject Headings

MeSH descriptor ID

C008661

Human Metabolome Database ID

14 March 2018

HMDB0029540

2 references

based on heuristic

inferred from InChIKey

3 references

nobiletin (English)

5 October 2016

inferred from InChIKey

UNII

D65ILJ7WLY

2 references

Global Substance Registration System

UNII

D65ILJ7WLY

English

title

NOBILETIN (English)

5 October 2016

0 references

1 reference

https://docs.openalex.org/download-snapshot/snapshot-data-format

nobiletin (English)

5 October 2016

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

26 January 2022

UMLS CUI

C0062638

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023