class name | count |
---|---|
asterids | 5 |
class name | count |
---|---|
Caprifoliaceae | 3 |
Asteraceae | 2 |
br08003 Category | # of metabolite |
---|---|
Others | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Others | C09743 | C00003197 |
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 |
---|---|---|---|---|---|---|
C00003197
![]() |
Valerenic acid
|
CHEMBL1545045
|
C037133
|
8 / 3 / 3 |
![]() |
|
C00017522
![]() |
6,7-Dehydroartemisinic acid
|
![]() |
||||
C00020390
![]() |
Aciphyllic acid
|
C047952
|
![]() |
|||
C00021291
![]() |
Valerenolic acid
/ Hydroxyvalerenic acid |
CHEMBL1565922
|
4 / 3 / 5 |
![]() |
||
C00021292
![]() |
Acetylvalerenolic acid
|
CHEMBL1401208
|
2 / 1 / 1 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q03181 | Peroxisome proliferator-activated receptor delta | NR1C2 | C00003197 C00021292 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00003197 C00021291 | 0 / 0 |
P04150 | Glucocorticoid receptor | NR3C1 | C00003197 C00021291 | 0 / 1 |
P19793 | Retinoic acid receptor RXR-alpha | NR2B1 | C00003197 | 0 / 0 |
P10145 | Interleukin-8 | Secreted protein | C00003197 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00003197 | 3 / 2 |
Q96RI1 | Bile acid receptor | NR1H4 | C00021291 | 0 / 0 |
P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00003197 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003197 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00021291 | 3 / 4 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00021292 | 1 / 1 |
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
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
KEGG | name | UniProt |
---|---|---|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
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)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|