Species

KNApSAcK Entry

Organism name Primula pulverulenta
Genus Primula
Family Primulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Primula pulverulenta
Linked NCBI taxonomy ID 166118
Linked level species

Family

Family in NCBI taxonomy Primulaceae
ID 4335

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (6)

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
C00003823 External link 512 5,2',5'-Trihydroxyflavone
No. 71 No. 15
C00003792 External link 512 5-Hydroxy-6-methoxyflavone
No. 76 No. 15
C00003803 External link 512 2',5'-Dihydroxyflavone
No. 76 No. 15
C00003802 External link 512 8,2'-Dihydroxyflavone
No. 76 No. 15
C00006993 External link 512 2'-beta-Dihydroxychalcone
CHEMBL1451434
6 / 10 / 7 No. 92 No. 13
C00003983 External link 512 2',5'-Dihydroxyflavone 5'-acetate
No. 4241

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00006993 4 / 1
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00006993 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00006993 2 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00006993 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00006993 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00006993 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (10)

OMIM preferred title UniProt
#119900 Digital clubbing, isolated congenital P15428
#600274 Frontotemporal dementia; ftd P10636
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (7)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)