id | C00002686 |
---|---|
Name | Acetosyringone |
CAS RN | 2478-38-8 |
Standard InChI | InChI=1S/C10H12O4/c1-6(11)7-4-8(13-2)10(12)9(5-7)14-3/h4-5,12H,1-3H3 |
Standard InChI (Main Layer) | InChI=1S/C10H12O4/c1-6(11)7-4-8(13-2)10(12)9(5-7)14-3/h4-5,12H,1-3H3 |
Phytochemical cluster | |
---|---|
KCF-S cluster | No. 1180 |
By standard InChI | CHEMBL224146 |
---|---|
By standard InChI Main Layer | CHEMBL224146 |
By LinkDB | C10664 |
---|
By CAS RN | C051667 |
---|
class name | count |
---|---|
Liliopsida | 2 |
asterids | 1 |
family name | count |
---|---|
Xanthorrhoeaceae | 1 |
Solanaceae | 1 |
Posidoniaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Bulbine narcissifolia | 49703 | Xanthorrhoeaceae | Liliopsida | Viridiplantae |
Nicotiana tabacum | 4097 | Solanaceae | asterids | Viridiplantae |
Posidonia oceanica | 55489 | Posidoniaceae | Liliopsida | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P02545 | Prelamin-A/C | Unclassified protein | CHEMBL224146 |
CHEMBL1614544
(1)
|
11 / 10 |
O75496 | Geminin | Unclassified protein | CHEMBL224146 |
CHEMBL2114843
(1)
|
0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL224146 |
CHEMBL2114738
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
KEGG | disease name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|