id | C00019505 |
---|---|
Name | 7-Hydroxy-2',4'-dimethoxyisoflavone |
CAS RN | 1891-01-6 |
Standard InChI | InChI=1S/C17H14O5/c1-20-11-4-6-12(15(8-11)21-2)14-9-22-16-7-10(18)3-5-13(16)17(14)19/h3-9,18H,1-2H3 |
Standard InChI (Main Layer) | InChI=1S/C17H14O5/c1-20-11-4-6-12(15(8-11)21-2)14-9-22-16-7-10(18)3-5-13(16)17(14)19/h3-9,18H,1-2H3 |
Phytochemical cluster | No. 15 |
---|---|
KCF-S cluster | No. 35 |
By standard InChI | CHEMBL1087126 |
---|---|
By standard InChI Main Layer | CHEMBL1087126 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
eudicotyledons | 1 |
family name | count |
---|---|
Papaveraceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Eschscholzia californica | 3467 | Papaveraceae | eudicotyledons | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL1087126 |
CHEMBL1614458
(1)
|
0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL1087126 |
CHEMBL1613910
(1)
|
3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL1087126 |
CHEMBL1614038
(1)
|
2 / 2 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | CHEMBL1087126 |
CHEMBL1614108
(1)
CHEMBL1613886
(1)
|
0 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL1087126 |
CHEMBL1613914
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
KEGG | disease name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|