Metabolite

KNApSAcK Entry

id C00007279
Name Ethanolamine
CAS RN 141-43-5
Standard InChI InChI=1S/C2H7NO/c3-1-2-4/h4H,1-3H2
Standard InChI (Main Layer) InChI=1S/C2H7NO/c3-1-2-4/h4H,1-3H2

Cluster

Phytochemical cluster
KCF-S cluster No. 8944

Link

ChEMBL

By standard InChI CHEMBL104943
By standard InChI Main Layer CHEMBL104943

KEGG

By LinkDB C00189

CTD

By CAS RN D019856

Species

Summary

Plant class

class name count
rosids 1

Family

family name count
Brassicaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Arabidopsis thaliana 3702 Brassicaceae rosids Viridiplantae

Human Protein / Gene in interaction

4 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 CHEMBL104943 CHEMBL1794524 (1) CHEMBL1794552 (1)
0 / 0
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL104943 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL104943 CHEMBL1614458 (1)
0 / 0
P03372 Estrogen receptor NR3A1 CHEMBL104943 CHEMBL1794364 (1)
1 / 1

CTD interaction (2)

compound gene gene name gene description interaction interaction type form reference
pmid
D019856 1950 EGF
HOMG4
URG
epidermal growth factor Ethanolamine results in increased activity of EGF protein increases activity
protein 15802876
D019856 2246 FGF1
AFGF
ECGF
ECGF-beta
ECGFA
ECGFB
FGF-1
FGF-alpha
FGFA
GLIO703
HBGF-1
HBGF1
fibroblast growth factor 1 (acidic) Ethanolamine results in increased activity of FGF1 protein increases activity
protein 15802876

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#615363 Estrogen resistance; estrr P03372
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (3)

KEGG disease name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)