Plant Species


Cumulative plant class count

class name count
eudicotyledons 1

Cumulative family count

class name count
Parmeliaceae 2
Aspergillaceae 1
Ochrolechiaceae 1
Amaranthaceae 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
C00017999 External link 512 NSC 249981
/ Lecanoric acid
CHEMBL1451874
C008263
10 / 8 / 13
C00018309 External link 512 Funicin
/ Ethericin B
C030874
C00046797 External link 512 Lecanorin
CHEMBL470647

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P00352 Retinal dehydrogenase 1 Enzyme C00017999 0 / 0
O75496 Geminin Unclassified protein C00017999 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00017999 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00017999 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00017999 2 / 2
P16050 Arachidonate 15-lipoxygenase Enzyme C00017999 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00017999 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00017999 0 / 0
O00255 Menin Unclassified protein C00017999 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00017999 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#119900 Digital clubbing, isolated congenital P15428
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255

KEGG DISEASE (13)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00036 Osteosarcoma P08684 (marker)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)