id | C00032667 |
---|---|
Name | 6,7,8-Trimethoxy-2H-1-benzopyran-2-one |
CAS RN | 6035-49-0 |
Standard InChI | InChI=1S/C12H12O5/c1-14-8-6-7-4-5-9(13)17-10(7)12(16-3)11(8)15-2/h4-6H,1-3H3 |
Standard InChI (Main Layer) | InChI=1S/C12H12O5/c1-14-8-6-7-4-5-9(13)17-10(7)12(16-3)11(8)15-2/h4-6H,1-3H3 |
Phytochemical cluster | No. 25 |
---|---|
KCF-S cluster | No. 364 |
By standard InChI | CHEMBL253551 |
---|---|
By standard InChI Main Layer | CHEMBL253551 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
asterids | 1 |
family name | count |
---|---|
Convolvulaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Cuscuta reflexa | 4129 | Convolvulaceae | asterids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P43166 | Carbonic anhydrase 7 | Lyase | CHEMBL253551 |
CHEMBL2341285
(1)
|
0 / 0 |
Q8N1Q1 | Carbonic anhydrase 13 | Lyase | CHEMBL253551 |
CHEMBL2341282
(1)
|
0 / 0 |
P00918 | Carbonic anhydrase 2 | Lyase | CHEMBL253551 |
CHEMBL2341286
(1)
|
1 / 2 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL253551 |
CHEMBL1614458
(1)
|
0 / 0 |
O43570 | Carbonic anhydrase 12 | Lyase | CHEMBL253551 |
CHEMBL2341283
(1)
|
1 / 2 |
P00915 | Carbonic anhydrase 1 | Lyase | CHEMBL253551 |
CHEMBL2341287
(1)
|
0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | CHEMBL253551 |
CHEMBL2341284
(1)
|
0 / 1 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL253551 |
CHEMBL1613910
(1)
|
3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL253551 |
CHEMBL1614038
(1)
|
2 / 2 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL253551 |
CHEMBL1613914
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#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
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
KEGG | disease name | UniProt |
---|---|---|
H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
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)
|