id | C00035785 |
---|---|
Name | 1-Penten-3-one |
CAS RN | 1629-58-9 |
Standard InChI | InChI=1S/C5H8O/c1-3-5(6)4-2/h3H,1,4H2,2H3 |
Standard InChI (Main Layer) | InChI=1S/C5H8O/c1-3-5(6)4-2/h3H,1,4H2,2H3 |
Phytochemical cluster | |
---|---|
KCF-S cluster | No. 8912 |
By standard InChI | CHEMBL1506228 |
---|---|
By standard InChI Main Layer | CHEMBL1506228 |
By LinkDB |
---|
By CAS RN | C057461 |
---|
class name | count |
---|---|
asterids | 1 |
family name | count |
---|---|
Solanaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Lycopersicon esculentum Mill. | 4081 | Solanaceae | asterids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P16473 | Thyrotropin receptor | Glycohormone receptor | CHEMBL1506228 |
CHEMBL1614281
(1)
CHEMBL1614361
(1)
|
3 / 2 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL1506228 |
CHEMBL1614458
(1)
|
0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | CHEMBL1506228 |
CHEMBL2114890
(1)
|
0 / 0 |
P10275 | Androgen receptor | NR3C4 | CHEMBL1506228 |
CHEMBL1794560
(1)
|
3 / 4 |
OMIM | preferred title | UniProt |
---|---|---|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
KEGG | disease name | UniProt |
---|---|---|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|