PCIDB

KNApSAcK Metabolite C00002981

Metabolite

KNApSAcK Entry

id C00002981
Name Bergenin
CAS RN 477-90-7
Standard InChI InChI=1S/C14H16O9/c1-21-11-5(16)2-4-7(9(11)18)12-13(23-14(4)20)10(19)8(17)6(3-15)22-12/h2,6,8,10,12-13,15-19H,3H2,1H3/t6-,8-,10+,12+,13-/m1/s1
Standard InChI (Main Layer) InChI=1S/C14H16O9/c1-21-11-5(16)2-4-7(9(11)18)12-13(23-14(4)20)10(19)8(17)6(3-15)22-12/h2,6,8,10,12-13,15-19H,3H2,1H3

Cluster

Phytochemical cluster
KCF-S cluster No. 4068

Link

ChEMBL

By standard InChI CHEMBL273019
By standard InChI Main Layer CHEMBL273019 CHEMBL1485130 CHEMBL1512567 CHEMBL1616426 CHEMBL1619590 CHEMBL1907330 CHEMBL1972686

KEGG

By LinkDB C09919

CTD

By CAS RN C006741

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase CHEMBL273019 CHEMBL1787667 (1)
1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL273019 CHEMBL1512567 CHEMBL2114810 (2)
7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL273019 CHEMBL1512567 CHEMBL1794401 (2)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#278300 Xanthinuria, type i P47989

KEGG DISEASE (4)

KEGG disease name UniProt
H00192 Xanthinuria P47989 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)