Species

KNApSAcK Entry

Organism name Stellaria dichotoma
Genus Stellaria
Family Caryophyllaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Stellaria
Linked NCBI taxonomy ID 13273
Linked level genus

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 (8)

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 External link 512 6,8-Di-C-galactopyranosylapigenin
CHEMBL1442950
C035195
6 / 14 / 8 No. 1 No. 15
C00006103 External link 512 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 External link 512 Dichotomine B
CHEMBL457820
No. 1551
C00026652 External link 512 Dichotomine A
CHEMBL379651
No. 1551
C00026656 External link 512 Dichotomide I
No. 2757
C00026657 External link 512 Dichotomide II
No. 2757
C00026655 External link 512 Dichotomine D
CHEMBL513088
No. 2851
C00026654 External link 512 Dichotomine C
/ (R)-(-)-Dichotomine C
CHEMBL458036
No. 2851

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

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 DISEASE (8)

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)