PCIDB

Pterocarpus spp.

Species

KNApSAcK Entry

Organism name Pterocarpus spp.
Genus Pterocarpus
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pterocarpus
Linked NCBI taxonomy ID 100169
Linked level genus

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (3)

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
C00002565 External link 512 Pseudobaptigenin
CHEMBL486176
C060800
3 / 5 / 3 No. 27 No. 15
C00009613 External link 512 Baphinitone
/ (-)-Homopterocarpin
/ 3,9-Dimethoxypterocarpan
CHEMBL277682
CHEMBL396671
CHEMBL2007304
No. 66 No. 15
C00009616 External link 512 Pterocarpin
/ 3-Methoxy-8,9-methylenedioxypterocarpan
CHEMBL21103
CHEMBL242128
CHEMBL1983713
7 / 8 / 10 No. 66 No. 15

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P13866 Sodium/glucose cotransporter 1 Glucose C00009616 1 / 1
P31639 Sodium/glucose cotransporter 2 Glucose C00009616 1 / 1
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002565 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002565 5 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00009616 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00009616 4 / 3
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00002565 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00009616 1 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00009616 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00009616 1 / 4

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#606824 Glucose/galactose malabsorption; ggm P13866
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#601665 Obesity P37231
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#233100 Renal glucosuria; glys1 P31639
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (13)

KEGG name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)