KCF-S cluster No. 190 (32 metabolites)

Corresponding Phytochemical cluster No. 13


Plant Species


Cumulative plant class count

class name count
rosids 45
asterids 3
Liliopsida 1

Cumulative family count

class name count
Fabaceae 23
Moraceae 20
Cannabaceae 2
Asteraceae 2
Apiaceae 1
Zingiberaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Chalcones 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Chalcones C08573 C00002371

Metabolite list (32)

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
C00002371 External link 512 Abyssinone VI
CHEMBL508727
1 / 0 / 0
C00007007 External link 512 Glyinflanin A
C00007010 External link 512 Glyinflanin E
C00007054 External link 512 Spinochalcone A
C00007072 External link 512 Kanzonol C
/ 2',4',4-Trihydroxy-3'-prenylchalcone
CHEMBL1644933
C00007073 External link 512 4,2',4'-Trihydroxy-3',5'-diprenylchalcone
CHEMBL403930
C00007113 External link 512 Antiarone E
C00007115 External link 512 Antiarone D
C00007116 External link 512 Antiarone C
C00007122 External link 512 Flemiwallichin E
C00007124 External link 512 Xanthoangelol
CHEMBL494083
CHEMBL457210
C068244
20 / 30 / 25 1 / 0
C00007128 External link 512 3'-Geranyl-2',4',6'-trihydroxychalcone
C00007137 External link 512 Kuwanol D
C00007138 External link 512 Ammothamnidin
C00007139 External link 512 Kushenol D
C00007142 External link 512 5-Deoxyhomoflemingin
C00007148 External link 512 Kuraridin
CHEMBL243362
3 / 2 / 2
C00007149 External link 512 Kuraridinol
C00007151 External link 512 Flemiwallichin C
C00007155 External link 512 Homoflemingin
C00011136 External link 512 Bartericin D
C00011138 External link 512 Angusticornin B
/ 3,5'-di-(2-Hydroxy-3-methylbut-3-enyl)-4,2',4'-trihydroxychalcone
C00011140 External link 512 Stipulin
CHEMBL1169874
C00011141 External link 512 Bartericin A
CHEMBL1169613
C00014441 External link 512 3'-Neryl-2',4',6'-trihydroxychalcone
C00014454 External link 512 Paratocarpin D
/ 3'-Prenyl-3-(2-hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxychalcone
C00014455 External link 512 Paratocarpin E
/ 3-Prenyl-3'-(2-hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxychalcone
C00014457 External link 512 Anthyllin
/ 5-Prenyl-3-(2-hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxychalcone
C00014471 External link 512 3'-Geranylchalconaringenin
/ 3'-Geranyl-4,2',4',6'-tetrahydroxychalcone
CHEMBL480722
C00014473 External link 512 5'-Prenylxanthohumol
/ 3',5'-Diprenyl-4,2',4'-trihydroxy-6-methoxychalcone
CHEMBL471777
C00014484 External link 512 3'-Geranyl-3,4,2',4'-tetrahydroxychalcone
CHEMBL258707
C00038202 External link 512 2',4'-Dihydroxy-3'-(1''-geranyl)-6'-methoxychalcone
CHEMBL255070

Human Protein / Gene in interactions

24 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002371 0 / 0
P13866 Sodium/glucose cotransporter 1 Glucose C00007148 1 / 1
P31639 Sodium/glucose cotransporter 2 Glucose C00007148 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00007124 0 / 0
Q99700 Ataxin-2 Unclassified protein C00007124 1 / 1
P10253 Lysosomal alpha-glucosidase Hydrolase C00007124 1 / 1
P02545 Prelamin-A/C Unclassified protein C00007124 11 / 10
P37840 Alpha-synuclein Unclassified protein C00007124 4 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00007124 1 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00007148 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00007124 0 / 0
P39748 Flap endonuclease 1 Enzyme C00007124 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007124 2 / 0
O75496 Geminin Unclassified protein C00007124 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00007124 0 / 0
P06280 Alpha-galactosidase A Enzyme C00007124 1 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00007124 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00007124 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00007124 4 / 3
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00007124 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00007124 1 / 0
O00255 Menin Unclassified protein C00007124 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00007124 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007124 1 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00007124

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (32)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#606824 Glucose/galactose malabsorption; ggm P13866
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#233100 Renal glucosuria; glys1 P31639
#275210 Restrictive dermopathy, lethal P02545
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (27)

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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00125 Fabry disease P06280 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (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)