PCIDB

KNApSAcK Metabolite C00031031

Metabolite

KNApSAcK Entry

id C00031031
Name (+)-Pinoresinol-beta-D-glucoside / Pinoresinol O-beta-D-glucopyranoside
CAS RN 69251-96-3
Standard InChI InChI=1S/C26H32O11/c1-32-18-7-12(3-5-16(18)28)24-14-10-35-25(15(14)11-34-24)13-4-6-17(19(8-13)33-2)36-26-23(31)22(30)21(29)20(9-27)37-26/h3-8,14-15,20-31H,9-11H2,1-2H3/t14-,15-,20+,21+,22-,23+,24+,25+,26+/m0/s1
Standard InChI (Main Layer) InChI=1S/C26H32O11/c1-32-18-7-12(3-5-16(18)28)24-14-10-35-25(15(14)11-34-24)13-4-6-17(19(8-13)33-2)36-26-23(31)22(30)21(29)20(9-27)37-26/h3-8,14-15,20-31H,9-11H2,1-2H3

Cluster

Phytochemical cluster No. 22
KCF-S cluster No. 174

Link

ChEMBL

By standard InChI CHEMBL1083218
By standard InChI Main Layer CHEMBL573336 CHEMBL1083218 CHEMBL1302893

KEGG

By LinkDB

CTD

By CAS RN

Human Protein / Gene in interaction

9 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme CHEMBL1302893 CHEMBL1614079 (1)
0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL1302893 CHEMBL1614076 (1)
1 / 1
P37840 Alpha-synuclein Unclassified protein CHEMBL1302893 CHEMBL2354282 (1)
4 / 2
Q9Y253 DNA polymerase eta Enzyme CHEMBL1302893 CHEMBL1794569 (1)
1 / 1
Q9UNA4 DNA polymerase iota Enzyme CHEMBL1302893 CHEMBL1794483 (1)
0 / 0
Q9UBT6 DNA polymerase kappa Enzyme CHEMBL1302893 CHEMBL1794536 (1)
0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL1302893 CHEMBL1613914 (1)
0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme CHEMBL1302893 CHEMBL1613829 (1)
0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme CHEMBL1302893 CHEMBL2114738 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#127750 Dementia, lewy body; dlb P37840
#232300 Glycogen storage disease ii P10253
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (4)

KEGG disease name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)