Species

KNApSAcK Entry

Organism name Crataegus pinnatifida
Genus Crataegus
Family Rosaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Crataegus pinnatifida
Linked NCBI taxonomy ID 510735
Linked level species

Family

Family in NCBI taxonomy Rosaceae
ID 3745

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (7)

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
C00005401 External link 512 Quercetin 3-robinoside
/ Quercetin 3-O-robinoside
/ Quercetin 3-O-robinobioside
/ Quercetin 3-O-rhamnosyl-(1->6)-galactoside
CHEMBL32579
CHEMBL310754
CHEMBL182108
CHEMBL226335
CHEMBL502782
CHEMBL1436093
CHEMBL1532989
25 / 18 / 16 No. 1 No. 15
C00005356 External link 512 Sexangularetin 3-glucoside
No. 2 No. 15
C00006369 External link 512 Vitexin 2''-acetate
No. 22 No. 15
C00014090 External link 512 Psilosin
/ Vitexin 6''-O-acetate
No. 22 No. 15
C00014089 External link 512 Vitexin 3''-O-acetate
No. 22 No. 15
C00014093 External link 512 8-C-beta-D-Glucofuranosylapigenin 2''-O-acetate
No. 22 No. 15
C00013613 External link 512 Pinnatifinoside A
/ (2R,3S,4S,5R)-4,5-Dihydro-3,4,5'-trihydroxy-5-(hydroxymethyl)-2'-(4-hydroxyphenyl)-spiro[furan-2(3H),8'(9'H)-[4H]furo[2,3-h][1]benzopyran]-4'-one
No. 2945

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P33527 Multidrug resistance-associated protein 1 drugs C00005401 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00005401 0 / 3
P06746 DNA polymerase beta Enzyme C00005401 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00005401 1 / 1
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00005401 1 / 1
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00005401 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00005401 1 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00005401 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00005401 0 / 0
P27487 Dipeptidyl peptidase 4 S9B C00005401 0 / 1
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00005401 0 / 0
P14679 Tyrosinase Oxidoreductase C00005401 4 / 2
P06276 Cholinesterase Hydrolase C00005401 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00005401 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00005401 3 / 3
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00005401 2 / 0
P03372 Estrogen receptor NR3A1 C00005401 1 / 1
P22303 Acetylcholinesterase Hydrolase C00005401 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00005401 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005401 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00005401 4 / 3
P48147 Prolyl endopeptidase S9A C00005401 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00005401 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00005401 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00005401 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#614490 Blood group, junior system; jr Q9UNQ0
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (16)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00032 Thyroid cancer P27487 (marker)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)