Species

KNApSAcK Entry

Organism name Cerastium arvense
Genus Cerastium
Family Caryophyllaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Cerastium arvense
Linked NCBI taxonomy ID 271558
Linked level species

Family

Family in NCBI taxonomy Caryophyllaceae
ID 3568

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (15)

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 External link 512 Cerarvensin 7-O-glucoside
No. 1 No. 15
C00006386 External link 512 Isomollupentin 2''-O-glucoside
No. 1 No. 15
C00006166 External link 512 6-C-beta-D-Xylopyranosyl-8-C-alpha-L-arabinopyranosylapigenin
No. 1 No. 15
C00006183 External link 512 Isocorymboside
CHEMBL1537012
7 / 2 / 2 No. 1 No. 15
C00006235 External link 512 6-C-Glucopyranosyl-8-C-galactopyranosylapigenin
CHEMBL1442950
6 / 14 / 8 No. 1 No. 15
C00006378 External link 512 Isovitexin 2''-O-xyloside
No. 1 No. 15
C00006385 External link 512 Isomollupentin 4'-O-glucoside
No. 1 No. 15
C00006384 External link 512 Isomollupentin 7-O-glucoside
No. 1 No. 15
C00006306 External link 512 Isomollupentin 7-O-glucoside-2''-O-arabinoside
No. 5 No. 15
C00006305 External link 512 Isomollupentin 7-O-glucoside-2''-O-xyloside
No. 5 No. 15
C00006322 External link 512 Isovitexin 7,2''-di-O-glucoside
No. 5 No. 15
C00006332 External link 512 Isovitexin 4'-O-glucoside 2''-O-(E)-ferulate
No. 7 No. 15
C00006331 External link 512 Isoorientin 4'-O-glucoside 2''-O-(E)-ferulate
No. 7 No. 15
C00006079 External link 512 Isomollupentin
/ 6-C-Arabinosylapigenin
/ 6-alpha-L-Arabinopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
No. 22 No. 15
C00006078 External link 512 Cerarvensin
/ 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-beta-D-xylopyranosyl-4H-1-benzopyran-4-one
No. 22 No. 15

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

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 DISEASE (9)

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)