Metabolite

KNApSAcK Entry

id C00027970
Name Broussonetinine A
CAS RN 173220-06-9
Standard InChI InChI=1S/C18H35NO5/c20-12-8-10-14(22)9-6-4-2-1-3-5-7-11-15-17(23)18(24)16(13-21)19-15/h15-21,23-24H,1-13H2/t15-,16-,17-,18+/m1/s1
Standard InChI (Main Layer) InChI=1S/C18H35NO5/c20-12-8-10-14(22)9-6-4-2-1-3-5-7-11-15-17(23)18(24)16(13-21)19-15/h15-21,23-24H,1-13H2

Cluster

Phytochemical cluster
KCF-S cluster No. 514

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL1373221

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
rosids 1

Family

family name count
Moraceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Broussonetia kazinoki 66380 Moraceae rosids Viridiplantae

Human Protein / Gene in interaction

4 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme CHEMBL1373221 CHEMBL1613818 (1)
6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL1373221 CHEMBL1614175 (1) CHEMBL1614076 (1)
CHEMBL1614103 (1) CHEMBL1614031 (1)
1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL1373221 CHEMBL1794401 (1)
0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL1373221 CHEMBL1613914 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#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 (5)

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)
H00069 Glycogen storage diseases (GSD) P10253 (related)