KCF-S cluster No. 491 (16 metabolites)

Corresponding Phytochemical cluster No. 25



Metabolite list (16)

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
C00002458 External link 512 Cichoriin
C410941
C00002472 External link 512 Esculin
CHEMBL359043
CHEMBL482581
CHEMBL1434042
CHEMBL1515174
CHEMBL1536019
CHEMBL1619714
CHEMBL1624854
D004929
22 / 18 / 24 0 / 1
C00002474 External link 512 Fraxin
CHEMBL293864
C080614
11 / 3 / 5
C00002500 External link 512 Scopolin
CHEMBL225024
C417572
7 / 3 / 4
C00019796 External link 512 Bergaptol-O-beta-D-glucopyranoside
C067416
C00019835 External link 512 (-)-2,3-Dihydro-9-O-beta-glucosyloxy-2-isopropenyl-7H-furo[3,2-g][1]benzopyran-7-one
C00019844 External link 512 6,7-Dihydroxy-5-methoxycoumarin 6-beta-D-glucopyranoside
C00019957 External link 512 5-Methoxy-8-O-beta-D-glucosyloxy-psoralen
C00030984 External link 512 Phellodenol G
C00030985 External link 512 Phellodenol H
C00032165 External link 512 Skimmin
/ (-)-Skimmin
CHEMBL526377
C00037003 External link 512 Daphnin
CHEMBL1879316
3 / 2 / 3
C00044063 External link 512 Gerberinside
/ 4-Hydroxy-5-methylcoumarin 4-O-beta-D-glucopyranoside
C058371
C00047445 External link 512 Euoniside
/ (+)-Euoniside
C00047500 External link 512 Mandshurin
C00047677 External link 512 5-Hydroxy-6-methoxy-7-O-beta-D-glucosylcoumarin

Human Protein / Gene in interactions

34 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00002472 C00002474 C00037003 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002472 C00002474 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00002474 C00002500 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00002474 C00002500 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00002474 C00002500 0 / 1
O43570 Carbonic anhydrase 12 Lyase C00002474 C00002500 1 / 2
P00918 Carbonic anhydrase 2 Lyase C00002474 C00002500 1 / 2
Q8N1Q1 Carbonic anhydrase 13 Lyase C00002474 C00002500 0 / 0
P42226 Signal transducer and activator of transcription 6 Unclassified protein C00002472 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002472 0 / 1
P11473 Vitamin D3 receptor NR1I1 C00037003 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002472 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002472 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002472 1 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002472 1 / 1
P04062 Glucosylceramidase Enzyme C00002472 6 / 4
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002472 0 / 3
P29466 Caspase-1 C14 C00002472 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00037003 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002472 0 / 0
P06280 Alpha-galactosidase A Enzyme C00002472 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002472 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002474 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002472 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002472 2 / 2
P22303 Acetylcholinesterase Hydrolase C00002500 1 / 0
P55210 Caspase-7 C14 C00002472 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002472 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002472 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00002474 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002472 0 / 0
O00255 Menin Unclassified protein C00002472 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002472 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002474 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (24)

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
#301500 Fabry disease P06280
#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
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#143860 Hyperchlorhidrosis, isolated O43570
#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
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#168600 Parkinson disease, late-onset; pd P04062
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#112100 Yt blood group antigen P22303

KEGG DISEASE (32)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
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)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D013272 Stomach Diseases C00002472