Plant Species


Cumulative plant class count

class name count
rosids 10
asterids 2
Euphyllophyta 1

Cumulative family count

class name count
Rutaceae 8
Solanaceae 2
Brassicaceae 2
Salviniaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

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
figure
C00007546 External link 512 Methylbenzoate
CHEMBL16435
4 / 6 / 6
C00034054 External link 512 Methyl benzoate
CHEMBL16435
C044605
4 / 6 / 6
C00034600 External link 512 Methyl anthranilate
CHEMBL1493986
C038892
3 / 3 / 3

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00007546 C00034054 C00034600 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00007546 C00034054 3 / 2
P10145 Interleukin-8 Secreted protein C00007546 C00034054 0 / 0
P10275 Androgen receptor NR3C4 C00007546 C00034054 3 / 4
P00352 Retinal dehydrogenase 1 Enzyme C00034600 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00034600 3 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (9)

KEGG name UniProt
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (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)