| Organism name | Cerastium arvense |
|---|---|
| Genus | Cerastium |
| Family | Caryophyllaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Cerastium arvense |
|---|---|
| Linked NCBI taxonomy ID | 271558 |
| Linked level | species |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00006388
|
Cerarvensin 7-O-glucoside
|
No. 1 | No. 15 |
|
||||
|
C00006386
|
Isomollupentin 2''-O-glucoside
|
No. 1 | No. 15 |
|
||||
|
C00006166
|
6-C-beta-D-Xylopyranosyl-8-C-alpha-L-arabinopyranosylapigenin
|
No. 1 | No. 15 |
|
||||
|
C00006183
|
Isocorymboside
|
CHEMBL1537012
|
7 / 2 / 2 | No. 1 | No. 15 |
|
||
|
C00006235
|
6-C-Glucopyranosyl-8-C-galactopyranosylapigenin
|
CHEMBL1442950
|
6 / 14 / 8 | No. 1 | No. 15 |
|
||
|
C00006378
|
Isovitexin 2''-O-xyloside
|
No. 1 | No. 15 |
|
||||
|
C00006385
|
Isomollupentin 4'-O-glucoside
|
No. 1 | No. 15 |
|
||||
|
C00006384
|
Isomollupentin 7-O-glucoside
|
No. 1 | No. 15 |
|
||||
|
C00006306
|
Isomollupentin 7-O-glucoside-2''-O-arabinoside
|
No. 5 | No. 15 |
|
||||
|
C00006305
|
Isomollupentin 7-O-glucoside-2''-O-xyloside
|
No. 5 | No. 15 |
|
||||
|
C00006322
|
Isovitexin 7,2''-di-O-glucoside
|
No. 5 | No. 15 |
|
||||
|
C00006332
|
Isovitexin 4'-O-glucoside 2''-O-(E)-ferulate
|
No. 7 | No. 15 |
|
||||
|
C00006331
|
Isoorientin 4'-O-glucoside 2''-O-(E)-ferulate
|
No. 7 | No. 15 |
|
||||
|
C00006079
|
Isomollupentin
/ 6-C-Arabinosylapigenin / 6-alpha-L-Arabinopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
No. 22 | No. 15 |
|
||||
|
C00006078
|
Cerarvensin
/ 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-beta-D-xylopyranosyl-4H-1-benzopyran-4-one |
No. 22 | No. 15 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00006183 C00006235 | 1 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006183 C00006235 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00006183 | 1 / 1 |
| P39748 | Flap endonuclease 1 | Enzyme | C00006183 | 0 / 0 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00006235 | 7 / 3 |
| P06746 | DNA polymerase beta | Enzyme | C00006183 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00006183 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00006235 | 6 / 4 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00006183 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00006235 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00006235 | 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
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
| 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)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|