class name | count |
---|---|
asterids | 3 |
class name | count |
---|---|
Asteraceae | 3 |
Lentinaceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00023266
![]() |
2,2-Dimethyl-6-vinylchroman-4-one
|
![]() |
||||
C00023271
![]() |
2,2-Dimethyl-6-(1-hydroxyethyl)chroman-4-one
|
![]() |
||||
C00036621
![]() |
6-Hydroxy-2,2-dimethylchroman-4-one
|
CHEMBL1384267
|
3 / 11 / 6 |
![]() |
||
C00042065
![]() |
2,2-Dimethyl-6-methoxy-4-chromanone
|
CHEMBL450517
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00036621 | 7 / 3 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00036621 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00036621 | 4 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|