flavone C-glycoside - Ontology Report - Rat Genome Database

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CHEBI ONTOLOGY - ANNOTATIONS

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The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

Term:	flavone C-glycoside	go back to main search page
Accession:	CHEBI:83280	browse the term
Definition:	Any C-glycosyl compound arising formally from the elimination of water from a glycosidic hydroxy group and an H atom bound to a flavone skeleton, thus creating a C-C bond.
Synonyms:	related_synonym:	flavone C-glycosides

show annotations for term's descendants Sort by:

Rat (9) Mouse (9) Human (9) Chinchilla (0) Bonobo (0) Dog (0) Squirrel (0) Pig (0) All
Genes (9)

isoorientin

term browser

Symbol

Object Name

Qualifiers

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

actin alpha 2, smooth muscle

multiple interactions

homoorientin inhibits the reaction [Ethanol results in increased expression of ACTA2 protein]

NCBI chr 1:252,537,614...252,550,394
Ensembl chr 1:252,537,615...252,550,394

G

AKT serine/threonine kinase 1

decreases phosphorylation
multiple interactions

homoorientin results in decreased phosphorylation of AKT1 protein
homoorientin promotes the reaction [Zinc Oxide analog results in decreased phosphorylation of AKT1 protein]; Zinc Oxide analog promotes the reaction [homoorientin results in decreased phosphorylation of AKT1 protein]

NCBI chr 6:137,218,398...137,239,970
Ensembl chr 6:137,218,376...137,236,258

G

BCL2, apoptosis regulator

multiple interactions

homoorientin inhibits the reaction [Ethanol results in increased expression of BCL2 mRNA]

NCBI chr13:26,605,426...26,769,374
Ensembl chr13:26,605,426...26,769,374

G

interleukin 6

multiple interactions

homoorientin inhibits the reaction [Ethanol results in increased expression of IL6 protein]

NCBI chr 4:3,043,231...3,047,807
Ensembl chr 4:3,043,231...3,047,807

G

mitogen activated protein kinase 1

multiple interactions

homoorientin promotes the reaction [Zinc Oxide analog results in decreased phosphorylation of MAPK1 protein]; Zinc Oxide analog promotes the reaction [homoorientin results in decreased phosphorylation of MAPK1 protein]

NCBI chr11:88,203,863...88,273,301
Ensembl chr11:88,211,599...88,273,254

G

mitogen activated protein kinase 3

multiple interactions

homoorientin promotes the reaction [Zinc Oxide analog results in decreased phosphorylation of MAPK3 protein]; Zinc Oxide analog promotes the reaction [homoorientin results in decreased phosphorylation of MAPK3 protein]

NCBI chr 1:198,192,773...198,198,975
Ensembl chr 1:198,192,773...198,198,975

G

myeloperoxidase

multiple interactions

homoorientin inhibits the reaction [Ethanol results in increased activity of MPO protein]

NCBI chr10:75,087,892...75,098,260
Ensembl chr10:75,087,892...75,098,260

G

transforming growth factor, beta 1

multiple interactions

homoorientin inhibits the reaction [Ethanol results in increased expression of TGFB1 protein]

NCBI chr 1:82,480,875...82,497,196
Ensembl chr 1:82,480,195...82,497,199

G

tumor necrosis factor

multiple interactions

homoorientin inhibits the reaction [Ethanol results in increased expression of TNF protein]

NCBI chr20:5,189,382...5,192,000
Ensembl chr20:5,189,390...5,192,000

Term paths to the root

Path 1
Term	Annotations
CHEBI ontology	19883
chemical entity	19883
atom	19881
nonmetal atom	19760
oxygen atom	19425
oxygen molecular entity	19425
flavonoids	10522
flavonoid	6379
flavones	4174
flavone C-glycoside	9
2''-O-rhamnosylscoparin	0
6,8-di-C-alpha-L-arabinosylapigenin	0
6-C-(alpha-L-arabinosyl)-8-C-(beta-L-arabinosyl)apigenin	0
6-C-(alpha-L-arabinosyl)-8-C-(beta-L-arabinosyl)chrysoeriol	0
6-C-[2'-O-alpha-L-rhamnopyranosyl-(1''->2')]-alpha-L-arabinopyranosylluteolin	0
6-C-[2-O-alpha-L-rhamnopyranosyl-(1''->2')]-beta-D-xylopyranosylluteolin	0
8-C-alpha-L-arabinopyranosyl-7-O-beta-D-glucopyranosylnaringenin	0
8-C-glucopyranosyl-6-C-xylopyranosylapigenin	0
acacetin-8-C-neohesperidoside	0
apigenin C-pentoside	0
cassiaoccidentalin B	0
fisetin 8-C-glucoside	0
isoorientin +	9
isoorientin 2''-O-glucoside	0
isoorientin 2''-O-rhamnoside +	0
isoorientin 7,3'-dimethyl ether	0
isoscoparin 2''-O-[6-(E)-feruloylglucoside]	0
isovitexin 2''-O-rhamnoside	0
luteolin 6-C-[beta-D-glucosyl-(1->2)-alpha-L-arabinoside]	0
maysin	0
mirificin	0
neocarlinoside	0
neoschaftoside	0
orientin 2''-O-rhamnoside	0
spinosin	0
swertiajaponin	0
swertisin	0
violanthin	0
Path 2
Term	Annotations
CHEBI ontology	19883
subatomic particle	19881
composite particle	19881
hadron	19881
baryon	19881
nucleon	19881
atomic nucleus	19881
atom	19881
main group element atom	19771
p-block element atom	19771
carbon group element atom	19679
carbon atom	19668
organic molecular entity	19668
heteroorganic entity	19257
organochalcogen compound	18964
organooxygen compound	18886
carbohydrates and carbohydrate derivatives	12267
carbohydrate	12267
carbohydrate derivative	11894
glycosyl compound	10944
C-glycosyl compound	236
flavone C-glycoside	9
2''-O-rhamnosylscoparin	0
6,8-di-C-alpha-L-arabinosylapigenin	0
6-C-(alpha-L-arabinosyl)-8-C-(beta-L-arabinosyl)apigenin	0
6-C-(alpha-L-arabinosyl)-8-C-(beta-L-arabinosyl)chrysoeriol	0
6-C-[2'-O-alpha-L-rhamnopyranosyl-(1''->2')]-alpha-L-arabinopyranosylluteolin	0
6-C-[2-O-alpha-L-rhamnopyranosyl-(1''->2')]-beta-D-xylopyranosylluteolin	0
8-C-alpha-L-arabinopyranosyl-7-O-beta-D-glucopyranosylnaringenin	0
8-C-glucopyranosyl-6-C-xylopyranosylapigenin	0
acacetin-8-C-neohesperidoside	0
apigenin C-pentoside	0
cassiaoccidentalin B	0
fisetin 8-C-glucoside	0
isoorientin +	9
isoorientin 2''-O-glucoside	0
isoorientin 2''-O-rhamnoside +	0
isoorientin 7,3'-dimethyl ether	0
isoscoparin 2''-O-[6-(E)-feruloylglucoside]	0
isovitexin 2''-O-rhamnoside	0
luteolin 6-C-[beta-D-glucosyl-(1->2)-alpha-L-arabinoside]	0
maysin	0
mirificin	0
neocarlinoside	0
neoschaftoside	0
orientin 2''-O-rhamnoside	0
spinosin	0
swertiajaponin	0
swertisin	0
violanthin	0

paths to the root