PCIDB

KNApSAcK Metabolite C00002038

Metabolite

KNApSAcK Entry

id C00002038
Name Fagomine
CAS RN 53185-12-9
Standard InChI InChI=1S/C6H13NO3/c8-3-4-6(10)5(9)1-2-7-4/h4-10H,1-3H2/t4-,5-,6-/m1/s1
Standard InChI (Main Layer) InChI=1S/C6H13NO3/c8-3-4-6(10)5(9)1-2-7-4/h4-10H,1-3H2

Cluster

Phytochemical cluster No. 1
KCF-S cluster No. 786

Link

ChEMBL

By standard InChI CHEMBL108084
By standard InChI Main Layer CHEMBL303545 CHEMBL108084 CHEMBL456583 CHEMBL505237 CHEMBL1818435 CHEMBL1818436 CHEMBL1818437 CHEMBL1818438 CHEMBL1818439

KEGG

By LinkDB C10144

CTD

By CAS RN C105643

Human Protein / Gene in interaction

5 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme CHEMBL108084 CHEMBL456583 CHEMBL505237 CHEMBL1818435 CHEMBL1818436 CHEMBL1818437 CHEMBL1818438 CHEMBL1818439 CHEMBL818908 (1) CHEMBL823890 (1)
CHEMBL993570 (1) CHEMBL1820866 (8)
6 / 4
Q14697 Neutral alpha-glucosidase AB Enzyme CHEMBL108084 CHEMBL456583 CHEMBL1818438 CHEMBL641729 (2) CHEMBL641730 (1)
CHEMBL645811 (2) CHEMBL645965 (3)
CHEMBL645968 (3) CHEMBL646085 (2)
CHEMBL646086 (1) CHEMBL822532 (1)
CHEMBL822537 (1)
0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL108084 CHEMBL993568 (1)
1 / 1
P04066 Tissue alpha-L-fucosidase Enzyme CHEMBL108084 CHEMBL456583 CHEMBL1818438 CHEMBL649569 (2) CHEMBL649571 (1)
1 / 2
Q9HCG7 Non-lysosomal glucosylceramidase Enzyme CHEMBL108084 CHEMBL456583 CHEMBL505237 CHEMBL1818435 CHEMBL1818436 CHEMBL1818437 CHEMBL1818438 CHEMBL1818439 CHEMBL2015864 (8)
1 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#230000 Fucosidosis P04066
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#232300 Glycogen storage disease ii P10253
#168600 Parkinson disease, late-onset; pd P04062
#614409 Spastic paraplegia 46, autosomal recessive; spg46 Q9HCG7

KEGG DISEASE (7)

KEGG disease name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00141 Fucosidosis P04066 (related)
H00422 Glycoproteinoses P04066 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)