class name | count |
---|---|
Magnoliophyta | 4 |
asterids | 2 |
rosids | 2 |
class name | count |
---|---|
Lauraceae | 4 |
Loganiaceae | 2 |
Erythroxylaceae | 1 |
Salicaceae | 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 |
---|---|---|---|---|---|---|
C00001661
![]() |
Ryanodine
|
CHEMBL24179
CHEMBL308183 CHEMBL352124 CHEMBL1486287 CHEMBL1742069 |
D012433
|
8 / 12 / 8 | 1 / 4 |
![]() |
C00034668
![]() |
Ryanodanol
/ (+)-Ryanodanol |
![]() |
||||
C00036450
![]() |
2,3-Didehydrocinnzeylanone
|
![]() |
||||
C00036672
![]() |
9-Hydroxy-10-epi-ryanodine
/ 9alpha-Hydroxy-10-epiryanodine |
![]() |
||||
C00037172
![]() |
Garajonone
|
![]() |
||||
C00050390
![]() |
Perseanol
|
CHEMBL517451
|
![]() |
|||
C00050407
![]() |
Vignaticol
|
CHEMBL517312
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001661 | 1 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00001661 | 2 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001661 | 0 / 1 |
P21817 | Ryanodine receptor 1 | CA | C00001661 | 4 / 2 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001661 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001661 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001661 | 0 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00001661 | 4 / 3 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
6261 | RYR1, CCO, MHS, MHS1, RYDR, RYR, RYR-1, SKRR | ryanodine receptor 1 (skeletal) |
C00001661
|
OMIM | preferred title | UniProt |
---|---|---|
#117000 | Central core disease of muscle |
P21817
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#145600 | Malignant hyperthermia, susceptibility to, 1; mhs1 |
P21817
|
#255320 | Minicore myopathy with external ophthalmoplegia |
P21817
|
#255310 | Myopathy, congenital, with fiber-type disproportion; cftd |
P21817
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00699 | Central core disease |
P21817
(related)
|
H01310 | Multi-minicore disease (MmD) |
P21817
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|