Species

KNApSAcK Entry

Organism name Triaenophora rupestris
Genus Triaenophora
Family Scrophulariaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Triaenophora rupestris
Linked NCBI taxonomy ID 441503
Linked level species

Family

Family in NCBI taxonomy
ID

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (4)

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
C00003075 External link 512 Catalpol
CHEMBL513223
C078040
2 / 1 / 1 0 / 2 No. 64 No. 36
C00010600 External link 512 Ajugol
/ Leonuride
CHEMBL595516
No. 64 No. 36
C00033820 External link 512 Epiloganic acid
CHEMBL1081585
CHEMBL1079678
CHEMBL1356464
CHEMBL1452775
6 / 8 / 7 No. 64 No. 36
C00033579 External link 512 6-Feruloyl ajugol
/ 6-O-(E)-Feruloyl ajugol
No. 287 No. 36

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P60033 CD81 antigen Unclassified protein C00033820 1 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme C00003075 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00033820 2 / 0
P03372 Estrogen receptor NR3A1 C00003075 1 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00033820 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00033820 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00033820 1 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00033820 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#613496 Immunodeficiency, common variable, 6; cvid6 P60033
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (8)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00026 Endometrial Cancer P03372 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00088 Common variable immunodeficiency (CVID) P60033 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D007249 Inflammation C00003075
D019636 Neurodegenerative Diseases C00003075