id | C00033558 |
---|---|
Name | E)-3,4-Dimethoxycinnamic acid / 3,4-Dimethoxy-trans-cinnamic acid |
CAS RN | 14737-89-4 |
Standard InChI | InChI=1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)/b6-4+ |
Standard InChI (Main Layer) | InChI=1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13) |
Phytochemical cluster | No. 6 |
---|---|
KCF-S cluster | No. 1366 |
By standard InChI | CHEMBL320295 |
---|---|
By standard InChI Main Layer | CHEMBL320295 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
rosids | 1 |
family name | count |
---|---|
Brassicaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Wasabia japonica | 75806 | Brassicaceae | rosids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | CHEMBL320295 |
CHEMBL1613842
(1)
|
4 / 2 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | CHEMBL320295 |
CHEMBL1014033
(1)
|
0 / 3 |
P11473 | Vitamin D3 receptor | NR1I1 | CHEMBL320295 |
CHEMBL1794311
(1)
|
2 / 3 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL320295 |
CHEMBL1614458
(1)
|
0 / 0 |
O75496 | Geminin | Unclassified protein | CHEMBL320295 |
CHEMBL2114780
(1)
|
0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | CHEMBL320295 |
CHEMBL1613808
(1)
|
0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL320295 |
CHEMBL1613910
(1)
|
3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL320295 |
CHEMBL1614038
(3)
|
2 / 2 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | CHEMBL320295 |
CHEMBL1614240
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL320295 |
CHEMBL1613914
(3)
|
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
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | disease name | UniProt |
---|---|---|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
Q16637 (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)
|