id | C00019845 |
---|---|
Name | 7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-5-methoxycoumarin |
CAS RN | 73435-98-0 |
Standard InChI | InChI=1S/C15H18O6/c1-15(2,18)13(16)8-20-12-7-10-9(6-11(12)19-3)4-5-14(17)21-10/h4-7,13,16,18H,8H2,1-3H3 |
Standard InChI (Main Layer) | InChI=1S/C15H18O6/c1-15(2,18)13(16)8-20-12-7-10-9(6-11(12)19-3)4-5-14(17)21-10/h4-7,13,16,18H,8H2,1-3H3 |
Phytochemical cluster | No. 25 |
---|---|
KCF-S cluster | No. 579 |
By standard InChI | CHEMBL1574904 |
---|---|
By standard InChI Main Layer | CHEMBL1574904 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
asterids | 1 |
family name | count |
---|---|
Asteraceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Pterocaulon alopecuroides | 81513 | Asteraceae | asterids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P06746 | DNA polymerase beta | Enzyme | CHEMBL1574904 |
CHEMBL1614079
(1)
|
0 / 0 |
P04062 | Glucosylceramidase | Enzyme | CHEMBL1574904 |
CHEMBL1613818
(1)
|
6 / 4 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | CHEMBL1574904 |
CHEMBL1794495
(1)
|
2 / 2 |
P06280 | Alpha-galactosidase A | Enzyme | CHEMBL1574904 |
CHEMBL1614217
(1)
CHEMBL1614369
(1)
|
1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL1574904 |
CHEMBL1794483
(1)
|
0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | CHEMBL1574904 |
CHEMBL1614211
(1)
|
0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | CHEMBL1574904 |
CHEMBL1794536
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL1574904 |
CHEMBL1613914
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#301500 | Fabry disease |
P06280
|
#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
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#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)
|
H00125 | Fabry disease |
P06280
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|