Species

KNApSAcK Entry

Organism name Morinda citrifolia L.,
Genus Morinda
Family Rubiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Morinda citrifolia
Linked NCBI taxonomy ID 43522
Linked level species

Family

Family in NCBI taxonomy Rubiaceae
ID 24966

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (12)

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
C00019420 External link 512 Physcion
/ 1,8-Dihydroxy-3-methyl-6-methoxyanthraquinone
CHEMBL42624
C008905
18 / 20 / 14 1 / 0 No. 41 No. 62
C00035974 External link 512 7-Hydroxy-8-methoxy-2-methylanthraquinone
No. 41 No. 62
C00032078 External link 512 Nordamnacanthal
No. 41 No. 62
C00031601 External link 512 Anthragallol 2-methyl ether
CHEMBL227588
No. 41 No. 62
C00031233 External link 512 Rubiadin-1-methyl ether
C079172
No. 41 No. 62
C00031591 External link 512 Alizarin 1-methyl ether
CHEMBL446748
C035010
No. 41 No. 62
C00031600 External link 512 Anthragallol 1,3-dimethyl ether
No. 41 No. 62
C00029570 External link 512 6alpha-Hydroxyadoxoside
No. 56 No. 36
C00029749 External link 512 Asperulosidic acid
CHEMBL389958
No. 100 No. 36
C00030093 External link 512 Deacetylasperulosidic acid
CHEMBL459415
No. 100 No. 36
C00031679 External link 512 Citrifolinin A
CHEMBL446254
No. 774
C00031680 External link 512 Yopaaoside A
/ (-)-Yopaaoside A
No. 774

Human Protein / Gene in interactions

18 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08246 Neutrophil elastase S1A C00019420 2 / 1
P11473 Vitamin D3 receptor NR1I1 C00019420 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00019420 0 / 0
P08311 Cathepsin G S1A C00019420 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00019420 0 / 0
Q9H244 P2Y purinoceptor 12 Purine receptor C00019420 1 / 1
P06280 Alpha-galactosidase A Enzyme C00019420 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00019420 2 / 2
P16050 Arachidonate 15-lipoxygenase Enzyme C00019420 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00019420 4 / 3
O43451 Maltase-glucoamylase, intestinal Hydrolase C00019420 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00019420 0 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00019420 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00019420 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00019420 0 / 1
P03372 Estrogen receptor NR3A1 C00019420 1 / 1
P09619 Platelet-derived growth factor receptor beta Pdgfr C00019420 5 / 1
P16234 Platelet-derived growth factor receptor alpha Pdgfr C00019420 2 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
581 BAX, BCL2L4 BCL2-associated X protein C00019420

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#615007 Basal ganglia calcification, idiopathic, 4; ibgc4 P09619
#609821 Bleeding disorder, platelet-type, 8; bdplt8 Q9H244
#162800 Cyclic neutropenia P08246
#119900 Digital clubbing, isolated congenital P15428
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#606764 Gastrointestinal stromal tumor; gist P16234
#607685 Hypereosinophilic syndrome, idiopathic; hes P16234
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#607785 Juvenile myelomonocytic leukemia; jmml P09619
#601626 Leukemia, acute myeloid; aml P09619
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#131440 Myeloproliferative disorder, chronic, with eosinophilia P09619
#228550 Myofibromatosis, infantile, 1; imf1 P09619
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (14)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
Q92731 (marker)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
H00100 Neutropenic disorders P08246 (related)
H00042 Glioma P09619 (related)
P16234 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01235 Bleeding disorder platelet-type Q9H244 (related)