| Organism name | Stellaria dichotoma |
|---|---|
| Genus | Stellaria |
| Family | Caryophyllaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Stellaria |
|---|---|
| Linked NCBI taxonomy ID | 13273 |
| Linked level | genus |
| Family in NCBI taxonomy | Caryophyllaceae |
|---|---|
| ID | 3568 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | eudicotyledons |
|---|---|
| ID | 71240 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00006234
|
6,8-Di-C-galactopyranosylapigenin
|
CHEMBL1442950
|
C035195
|
6 / 14 / 8 | No. 1 | No. 15 |
|
|
|
C00006103
|
6-C-Galactosylisoscutellarein
/ 6-beta-D-Galactopyranosyl-5,7,8-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
C035194
|
No. 22 | No. 15 |
|
|||
|
C00026653
|
Dichotomine B
|
CHEMBL457820
|
No. 1551 |
|
||||
|
C00026652
|
Dichotomine A
|
CHEMBL379651
|
No. 1551 |
|
||||
|
C00026656
|
Dichotomide I
|
No. 2757 |
|
|||||
|
C00026657
|
Dichotomide II
|
No. 2757 |
|
|||||
|
C00026655
|
Dichotomine D
|
CHEMBL513088
|
No. 2851 |
|
||||
|
C00026654
|
Dichotomine C
/ (R)-(-)-Dichotomine C |
CHEMBL458036
|
No. 2851 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00006234 | 6 / 4 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00006234 | 1 / 1 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00006234 | 7 / 3 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006234 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00006234 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00006234 | 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)
|