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 |
Phytochemical cluster | |
---|---|
KCF-S cluster | No. 514 |
By standard InChI | |
---|---|
By standard InChI Main Layer | CHEMBL1373221 |
By LinkDB |
---|
By CAS RN |
---|
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Broussonetia kazinoki | 66380 | Moraceae | rosids | Viridiplantae |
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 |
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 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)
|