id | C00010196 |
---|---|
Name | Serratin / 5,7-Dihydroxy-4-phenylcoumarin |
CAS RN | 7758-73-8 |
Standard InChI | InChI=1S/C15H10O4/c16-10-6-12(17)15-11(9-4-2-1-3-5-9)8-14(18)19-13(15)7-10/h1-8,16-17H |
Standard InChI (Main Layer) | InChI=1S/C15H10O4/c16-10-6-12(17)15-11(9-4-2-1-3-5-9)8-14(18)19-13(15)7-10/h1-8,16-17H |
Phytochemical cluster | No. 17 |
---|---|
KCF-S cluster | No. 54 |
By standard InChI | CHEMBL600635 |
---|---|
By standard InChI Main Layer | CHEMBL600635 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
rosids | 1 |
family name | count |
---|---|
Passifloraceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Passiflora serratodigitata | 231192 | Passifloraceae | rosids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | CHEMBL600635 |
CHEMBL2114784
(1)
|
1 / 1 |
P37840 | Alpha-synuclein | Unclassified protein | CHEMBL600635 |
CHEMBL2354282
(1)
|
4 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | CHEMBL600635 |
CHEMBL1614166
(1)
|
1 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | CHEMBL600635 |
CHEMBL1738606
(1)
|
0 / 0 |
P51679 | C-C chemokine receptor type 4 | CC chemokine receptor | CHEMBL600635 |
CHEMBL1072092
(1)
|
0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | CHEMBL600635 |
CHEMBL1738588
(1)
|
0 / 0 |
Q9GZV3 | High affinity choline transporter 1 | Choline Na-symporter | CHEMBL600635 |
CHEMBL1794362
(1)
|
1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | CHEMBL600635 |
CHEMBL2114913
(1)
|
0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#127750 | Dementia, lewy body; dlb |
P37840
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#158580 | Neuronopathy, distal hereditary motor, type viia; hmn7a |
Q9GZV3
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
KEGG | disease name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|