PCIDB

KNApSAcK Metabolite C00011939

Metabolite

KNApSAcK Entry

id C00011939
Name Fraxinellone
CAS RN 28808-62-0
Standard InChI InChI=1S/C14H16O3/c1-9-4-3-6-14(2)11(9)13(15)17-12(14)10-5-7-16-8-10/h5,7-8,12H,3-4,6H2,1-2H3/t12-,14+/m0/s1
Standard InChI (Main Layer) InChI=1S/C14H16O3/c1-9-4-3-6-14(2)11(9)13(15)17-12(14)10-5-7-16-8-10/h5,7-8,12H,3-4,6H2,1-2H3

Cluster

Phytochemical cluster
KCF-S cluster No. 1461

Link

ChEMBL

By standard InChI CHEMBL257170
By standard InChI Main Layer CHEMBL257170 CHEMBL1595442

KEGG

By LinkDB

CTD

By CAS RN C075391

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL1595442 CHEMBL1614103 (1) CHEMBL1614031 (1)
1 / 1
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL1595442 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein CHEMBL1595442 CHEMBL2354287 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#232300 Glycogen storage disease ii P10253
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (4)

KEGG disease name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)