PCIDB

KNApSAcK Metabolite C00036799

Metabolite

KNApSAcK Entry

id C00036799
Name beta-Homonojirimycin
CAS RN 157544-15-5
Standard InChI InChI=1S/C7H15NO5/c9-1-3-5(11)7(13)6(12)4(2-10)8-3/h3-13H,1-2H2/t3-,4+,5-,6+,7+
Standard InChI (Main Layer) InChI=1S/C7H15NO5/c9-1-3-5(11)7(13)6(12)4(2-10)8-3/h3-13H,1-2H2

Cluster

Phytochemical cluster
KCF-S cluster No. 667

Link

ChEMBL

By standard InChI CHEMBL2093897
By standard InChI Main Layer CHEMBL87169 CHEMBL320116 CHEMBL327137 CHEMBL501355 CHEMBL1169500 CHEMBL2093079 CHEMBL2093897 CHEMBL2111688 CHEMBL2114210 CHEMBL2115215

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
Liliopsida 1

Family

family name count
Araceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Aglaonema treubii 174181 Araceae Liliopsida Viridiplantae

Human Protein / Gene in interaction

6 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme CHEMBL501355 CHEMBL993570 (1)
6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL501355 CHEMBL993567 (1) CHEMBL993579 (1)
1 / 1
P04066 Tissue alpha-L-fucosidase Enzyme CHEMBL87169 CHEMBL320116 CHEMBL327137 CHEMBL501355 CHEMBL1169500 CHEMBL2093897 CHEMBL2111688 CHEMBL2114210 CHEMBL2115215 CHEMBL884024 (3) CHEMBL649579 (3)
CHEMBL649754 (1) CHEMBL648952 (3)
1 / 2
Q8TET4 Neutral alpha-glucosidase C Enzyme CHEMBL320116 CHEMBL327137 CHEMBL501355 CHEMBL2111688 CHEMBL647155 (2) CHEMBL876748 (2)
0 / 0
P06280 Alpha-galactosidase A Enzyme CHEMBL87169 CHEMBL501355 CHEMBL1169500 CHEMBL2093897 CHEMBL2114210 CHEMBL2115215 CHEMBL679754 (2) CHEMBL679755 (4)
1 / 1
O43451 Maltase-glucoamylase, intestinal Hydrolase CHEMBL87169 CHEMBL501355 CHEMBL1169500 CHEMBL2093897 CHEMBL2114210 CHEMBL2115215 CHEMBL649260 (4) CHEMBL649261 (1)
CHEMBL649328 (3) CHEMBL816395 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#301500 Fabry disease P06280
#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

KEGG DISEASE (8)

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)
H00125 Fabry disease P06280 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)