Plant Species


Cumulative plant class count

class name count
rosids 15

Cumulative family count

class name count
Rutaceae 15

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (14)

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
C00029988 External link 512 Clauslactone M
C00030242 External link 512 Excavatin E
C00030243 External link 512 Excavatin G
C00032840 External link 512 Clauslactone N
/ (+)-Clauslactone N
C00032841 External link 512 Clauslactone O
/ (+)-Clauslactone O
C00032842 External link 512 Clauslactone P
/ (-)-Clauslactone P
C00035269 External link 512 Clauslactone E
CHEMBL488603
C00036005 External link 512 3'',4''-Dihydrocapnolactone
C00039188 External link 512 Excavatin D
/ (+)-Excavatin D
CHEMBL1348986
4 / 13 / 8
C00039189 External link 512 Excavatin F
C00039190 External link 512 Excavatin H
C00039191 External link 512 Excavatin I
/ (+)-Excavatin I
C00039192 External link 512 Excavatin J
/ (+)-Excavatin J
CHEMBL470443
C00046676 External link 512 Clauslactone I
/ (+)-Clauslactone I
CHEMBL470443

Human Protein / Gene in interactions

4 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P17405 Sphingomyelin phosphodiesterase Enzyme C00039188 2 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00039188 7 / 3
P10636 Microtubule-associated protein tau Unclassified protein C00039188 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00039188 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#600274 Frontotemporal dementia; ftd P10636
#174800 Mccune-albright syndrome; mas P63092
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (8)

KEGG name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)