Plant Species


Cumulative plant class count

class name count
asterids 13

Cumulative family count

class name count
Lamiaceae 8
Asteraceae 5

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

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
figure
C00022268 External link 512 Hispanolone
CHEMBL1482813
CHEMBL2000054
2 / 4 / 3
C00022275 External link 512 Solidagenone
CHEMBL1475550
C406719
7 / 9 / 10
C00022294 External link 512 Marrubenol
CHEMBL389065
C00022394 External link 512 Ballotenol
C00022780 External link 512 2alpha-Hydroxy-3-oxo-4betaH-ent-cleroda-13(16),14-diene-15,16-oxide
C00022781 External link 512 2alpha,3alpha,4beta-Trihydroxy-ent-cleroda-13(16),14-diene-15,16-oxide
C00031960 External link 512 Leoheterin
/ (+)-Leoheterin

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10636 Microtubule-associated protein tau Unclassified protein C00022268 C00022275 4 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00022268 C00022275 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00022275 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00022275 2 / 3
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00022275 3 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00022275 0 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00022275 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#600274 Frontotemporal dementia; ftd P10636
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#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 (10)

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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)