| Organism name | Viola tricolor |
|---|---|
| Genus | Viola |
| Family | Violaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Viola tricolor |
|---|---|
| Linked NCBI taxonomy ID | 214053 |
| Linked level | species |
| Family in NCBI taxonomy | Violaceae |
|---|---|
| ID | 24921 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| Species | Activity |
|---|---|
| Viola tricolor L. | Analgesic |
| Viola tricolor L. | Antiinflammatory |
| Viola tricolor L. | Antioxidant |
| Viola tricolor L. | Antiseptic |
| Viola tricolor L. | Demulcent |
| Viola tricolor L. | Depurative |
| Viola tricolor L. | Diaphoretic |
| Viola tricolor L. | Diuretic |
| Viola tricolor L. | Emetic |
| Viola tricolor L. | Expectorant |
| Viola tricolor L. | Hemolytic |
| Viola tricolor L. | Laxative |
| Viola tricolor L. | Metabolic Stimulant |
| Viola tricolor L. | Natriuretic |
| Viola tricolor L. | Sedative |
| Viola tricolor L. | Stimulant |
| Viola tricolor L. | Tineacide |
| Viola tricolor L. | Vulnerary |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
|
C00006230
|
Violanthin
|
No. 1 | No. 15 |
|
||||
|
C00006229
|
Vicenin 2
/ Apigenin 6,8-di-C-glucoside |
CHEMBL1442950
|
6 / 14 / 8 | No. 1 | No. 15 |
|
||
|
C00006893
|
Violanin
/ Delphinidin 3-[6-(4-(E)-p-coumarylrhamnosyl)glucoside]-5-glucoside |
No. 7 | No. 15 |
|
||||
|
C00003787
|
Violaxanthin
|
C005613
|
No. 114 | No. 59 |
|
|||
|
C00022950
|
Mutatoxanthin
/ (3S,3'R,5R)-5,8-Epoxy-5,8-dihydro-beta,beta-carotene-3,3'-diol |
No. 664 | No. 59 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00006229 | 6 / 4 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00006229 | 1 / 1 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00006229 | 7 / 3 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006229 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00006229 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00006229 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #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
|
| KEGG | name | UniProt |
|---|---|---|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|