Metabolite

KNApSAcK Entry

id C00007928
Name 2',4',6'-Trihydroxydihydrochalcone / 3-Phenyl-1-(2,4,6-trihydroxyphenyl)-1-propanone
CAS RN 1088-08-0
Standard InChI InChI=1S/C15H14O4/c16-11-8-13(18)15(14(19)9-11)12(17)7-6-10-4-2-1-3-5-10/h1-5,8-9,16,18-19H,6-7H2
Standard InChI (Main Layer) InChI=1S/C15H14O4/c16-11-8-13(18)15(14(19)9-11)12(17)7-6-10-4-2-1-3-5-10/h1-5,8-9,16,18-19H,6-7H2

Cluster

Phytochemical cluster No. 13
KCF-S cluster No. 90

Link

ChEMBL

By standard InChI CHEMBL503375
By standard InChI Main Layer CHEMBL503375

KEGG

By LinkDB

CTD

By CAS RN

Human Protein / Gene in interaction

8 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL503375 CHEMBL1614076 (1)
1 / 1
Q96LD8 Sentrin-specific protease 8 Enzyme CHEMBL503375 CHEMBL2114850 (1) CHEMBL2114829 (1)
0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor CHEMBL503375 CHEMBL2114788 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL503375 CHEMBL1794483 (1)
0 / 0
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL503375 CHEMBL1737991 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL503375 CHEMBL1614502 (1)
4 / 3
O94925 Glutaminase kidney isoform, mitochondrial Enzyme CHEMBL503375 CHEMBL2114738 (1)
0 / 0
Q9HCT0 Fibroblast growth factor 22 Unclassified protein CHEMBL503375 CHEMBL2354256 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (4)

KEGG disease name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)