KCF-S cluster No. 466 (17 metabolites)

Corresponding Phytochemical cluster No. 25


Plant Species


Cumulative plant class count

class name count
asterids 27
rosids 19
eudicotyledons 1

Cumulative family count

class name count
Rutaceae 18
Apiaceae 18
Asteraceae 9
Picrodendraceae 1
Plumbaginaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Coumarins 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Coumarins C09280 C00002488

Metabolite list (17)

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
C00000577 External link 512 Gerberacoumarin
C00002488 External link 512 Osthol
/ Osthole
CHEMBL52229
C046627
12 / 6 / 5 7 / 4
C00019782 External link 512 Anisocoumarin B
C00019809 External link 512 Capensin
CHEMBL1327256
18 / 11 / 10
C00019847 External link 512 7-(3,3-Dimethylallyloxy)-6-hydroxy-5-methoxycoumarin
C00019871 External link 512 4-[5-Formyl-3-methyl-pent-2E,4E-dien-1-yl]-5-methylcoumarin
C00020012 External link 512 7-Methoxy-6-[(3-methyl-2-butenyl)oxy]coumarin
C00022705 External link 512 7-Isopentenyloxycoumarin
CHEMBL156692
9 / 1 / 2
C00033197 External link 512 Micromarin F
C00034856 External link 512 Haplopinol
C00034885 External link 512 Prenyletin
CHEMBL607536
9 / 2 / 3
C00036085 External link 512 Cedrecoumarin B
/ Microfolicoumarin
C00036889 External link 512 Cedrelopsin
C00037581 External link 512 O-Methylcedrelopsin
CHEMBL1338393
2 / 0 / 0
C00037864 External link 512 Suberosin
CHEMBL1928409
1 / 0 / 0
C00044069 External link 512 7-(3-Methyl-2-butenyloxy)-6-methoxycoumarin
CHEMBL594886
C00045592 External link 512 7-Methoxy-5-prenyloxy-coumarin
CHEMBL513279
1 / 1 / 0

Human Protein / Gene in interactions

35 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
B2RXH2 Lysine-specific demethylase 4E Enzyme C00019809 C00022705 C00034885 C00037581 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002488 C00022705 C00034885 0 / 0
P56817 Beta-secretase 1 A1A C00002488 C00022705 C00037864 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002488 C00019809 C00034885 0 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00002488 C00022705 C00037581 0 / 0
P55210 Caspase-7 C14 C00019809 C00034885 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00019809 C00022705 0 / 0
P29466 Caspase-1 C14 C00019809 C00034885 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00019809 C00022705 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002488 C00019809 0 / 0
O75496 Geminin Unclassified protein C00002488 C00019809 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00019809 1 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00022705 1 / 2
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002488 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002488 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00022705 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00034885 0 / 0
P39748 Flap endonuclease 1 Enzyme C00019809 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00019809 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00034885 2 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00019809 0 / 1
P22303 Acetylcholinesterase Hydrolase C00045592 1 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002488 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00019809 1 / 1
P04062 Glucosylceramidase Enzyme C00002488 6 / 4
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002488 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00019809 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00034885 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00019809 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00022705 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00034885 0 / 0
O14980 Exportin-1 Unclassified protein C00002488 0 / 0
Q99700 Ataxin-2 Unclassified protein C00019809 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00019809 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00019809 1 / 1

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2180 ACSL1, ACS1, FACL1, FACL2, LACS, LACS1, LACS2 acyl-CoA synthetase long-chain family member 1 (EC:6.2.1.3) C00002488
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00002488
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00002488
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002488
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002488
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00002488
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002488

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (21)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#612219 Ewing sarcoma; es P11308
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#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
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#112100 Yt blood group antigen P22303

KEGG DISEASE (18)

KEGG name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
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)
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
C538231 Adenocarcinoma of lung C00002488
D003920 Diabetes Mellitus C00002488
D006943 Hyperglycemia C00002488
D009361 Neoplasm Invasiveness C00002488