KCF-S cluster No. 133 (40 metabolites)

Corresponding Phytochemical cluster No. 13


Plant Species


Cumulative plant class count

class name count
rosids 57
asterids 28

Cumulative family count

class name count
Fabaceae 41
Asteraceae 18
Apiaceae 10
Moraceae 9
Cannabaceae 6
Euphorbiaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Chalcones 3

metabolites link (4)

br08003 Category KEGG ID KNApSAcK ID
Chalcones C08648 C00002381
Chalcones C16417 C00007099
Chalcones C16416 C00035575
Chalcones C08648 C00036579

Metabolite list (40)

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
C00002381 External link 512 Corylifolinin
/ Isobavachalcone
/ 2',4,4'-Trihydroxy-3'-(3-methyl-2-butenyl)chalcone
CHEMBL253467
C468754
8 / 22 / 21
C00007045 External link 512 Isocordoin
CHEMBL460618
C00007052 External link 512 Derricin
CHEMBL455982
C00007053 External link 512 Derricidin
CHEMBL450771
2 / 1 / 1
C00007056 External link 512 Licochalcone C
CHEMBL141207
1 / 0 / 0
C00007064 External link 512 4-Hydroxyderricin
CHEMBL458094
C068243
17 / 27 / 26
C00007065 External link 512 Xanthoangelol D
CHEMBL1711961
6 / 15 / 41
C00007066 External link 512 Xanthoangelol E
CHEMBL1718454
10 / 21 / 44
C00007067 External link 512 4-Hydroxycordoin
CHEMBL460400
1 / 0 / 0
C00007068 External link 512 Broussochalcone B
CHEMBL464428
1 / 2 / 2
C00007070 External link 512 Bavachalcone
C00007078 External link 512 Desmethylisoxanthohumol
CHEMBL2203298
C00007081 External link 512 Isoxanthohumol(Helichrysum)
C00007083 External link 512 2',4'-Dihydroxy-6'-methoxy-3'-prenylchalcone
C00007085 External link 512 Ovalichalcone
C00007086 External link 512 2',6'-Dihydroxy-4'-prenyloxychalcone
C00007087 External link 512 2'-Hydroxy-6'-methoxy-4'-prenyloxychalcone
C00007089 External link 512 Licochalcone D
CHEMBL1644932
C00007091 External link 512 Morachalcone A
CHEMBL465880
1 / 2 / 2
C00007095 External link 512 Broussochalcone A
CHEMBL115452
C106525
2 / 2 / 2
C00007099 External link 512 Xanthohumol
CHEMBL253896
6 / 0 / 1
C00007100 External link 512 4'-O-Methylxanthohumol
CHEMBL466335
C00007101 External link 512 4,2',6'-Trihydroxy-4'-prenyloxychalcone
C00007125 External link 512 Xanthoangelol B
CHEMBL494082
13 / 11 / 5
C00007159 External link 512 Xanthoangelol C
C00014450 External link 512 Psorachalcone A
CHEMBL428420
C00014456 External link 512 Licoagrochalcone A
/ 3-Prenyl-4,2',4'-trihydroxychalcone
CHEMBL229885
2 / 2 / 2
C00014460 External link 512 Xanthoangelol F
/ 3'-Geranyl-2',4-dihydroxy-4'-methoxychalcone
CHEMBL1722838
8 / 6 / 6
C00014461 External link 512 Xanthoangelol G
/ 3'-(3,7-Dimethyl-6-hydroxyocta-2,7-dienyl)-4,2'-dihydroxy-4'-methoxychalcone
CHEMBL1823414
C00014472 External link 512 Xanthohumol D
/ 3'-(2-Hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxy-6'-methoxychalcone
CHEMBL479500
C00014475 External link 512 Xanthogalenol
/ 3'-Prenyl-4,2',6'-trihydroxy-4'-methoxychalcone
CHEMBL466334
C00014487 External link 512 Licoagrochalcone C
/ 3-Prenyl-4,3',4'-trihydroxy-2-methoxychalcone
C00014491 External link 512 Ramosismin
/ 3'-Prenyl-2,4,5,2',4'-pentahydroxychalcone
C00014492 External link 512 3'-Prenyl-2',6',beta-trihydroxy-4'-methoxychalcone
C00033900 External link 512 Helichrysone A
C00035575 External link 512 Desmethylxanthohumol
CHEMBL466143
1 / 4 / 1
C00035796 External link 512 5-Prenylbutein
CHEMBL253677
C00036579 External link 512 4-Hydroxyisocordoin
CHEMBL253467
8 / 22 / 21
C00040675 External link 512 Xanthokeismin A
CHEMBL503569
C00041964 External link 512 Xanthoangelol J
CHEMBL491512

Human Protein / Gene in interactions

47 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002381 C00007068 C00007091 C00007095 C00014456 C00036579 2 / 2
O75164 Lysine-specific demethylase 4A Enzyme C00007064 C00007065 C00007066 C00007125 C00014460 0 / 0
Q99700 Ataxin-2 Unclassified protein C00007064 C00007066 C00007125 C00014460 1 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00007064 C00007065 C00007125 C00014460 0 / 0
O75496 Geminin Unclassified protein C00007064 C00007065 C00007066 C00007125 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007064 C00007066 C00007125 C00014460 2 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00007056 C00007095 C00014456 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007064 C00007065 C00007125 1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00007065 C00007066 C00007125 7 / 3
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00007064 C00007066 C00014460 1 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00002381 C00036579 2 / 3
P04637 Cellular tumor antigen p53 Transcription Factor C00007065 C00007066 7 / 37
Q9UNA4 DNA polymerase iota Enzyme C00007064 C00014460 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00002381 C00036579 4 / 5
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00002381 C00036579 4 / 3
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00002381 C00036579 1 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00002381 C00036579 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00007064 C00014460 0 / 3
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00002381 C00036579 9 / 3
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002381 C00036579 1 / 8
P17405 Sphingomyelin phosphodiesterase Enzyme C00007066 C00014460 2 / 2
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00007064 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00007053 0 / 0
O15530 3-phosphoinositide-dependent protein kinase 1 Pdk1 C00007099 0 / 0
Q9BQF6 Sentrin-specific protease 7 Enzyme C00007125 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00007066 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00007064 0 / 0
Q9GZR1 Sentrin-specific protease 6 Enzyme C00007125 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00007099 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00007099 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00007067 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00007053 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00007125 0 / 0
P42574 Caspase-3 C14 C00007125 0 / 0
P31749 RAC-alpha serine/threonine-protein kinase Akt C00035575 4 / 1
P37840 Alpha-synuclein Unclassified protein C00007064 4 / 2
Q96LD8 Sentrin-specific protease 8 Enzyme C00007125 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00007064 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00007066 0 / 0
P02545 Prelamin-A/C Unclassified protein C00007064 11 / 10
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00007064 0 / 0
Q04759 Protein kinase C theta type Delta C00007099 0 / 1
O00255 Menin Unclassified protein C00007064 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00007064 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00007125 0 / 0
P17252 Protein kinase C alpha type Alpha C00007099 0 / 0
P45984 Mitogen-activated protein kinase 9 Jnk C00007099 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (69)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#207410 Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 P21802
#101200 Apert syndrome P21802
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#123790 Beare-stevenson cutis gyrata syndrome; bstvs P21802
#614592 Bent bone dysplasia syndrome; bbds P21802
#114480 Breast cancer P31749
#300615 Brunner syndrome P21397
#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 P31749
P84022
#615109 Cowden syndrome 6; cws6 P31749
#123500 Crouzon syndrome P21802
#127750 Dementia, lewy body; dlb P37840
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#606764 Gastrointestinal stromal tumor; gist P10721
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#602089 Hemangioma, capillary infantile P35968
#114550 Hepatocellular carcinoma P08581
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#147950 Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 P11362
#123150 Jackson-weiss syndrome; jws P21802
#149730 Lacrimoauriculodentodigital syndrome; ladd P21802
#601626 Leukemia, acute myeloid; aml P10721
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P00533
P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#166250 Osteoglophonic dysplasia; ogd P11362
#260500 Papilloma of choroid plexus; cpp P04637
#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
#101600 Pfeiffer syndrome P11362
P21802
#172700 Pick disease of brain P10636
#172800 Piebald trait; pbt P10721
#102200 Pituitary adenoma, growth hormone-secreting P63092
#176920 Proteus syndrome P31749
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#275210 Restrictive dermopathy, lethal P02545
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#273300 Testicular germ cell tumor; tgct P10721
#190440 Trigonocephaly 1; trigno1 P11362
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (83)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
H00018 Gastric cancer P00533 (related)
P04637 (related)
P08581 (related)
P21802 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P04637 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P08581 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
P08581 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
H00170 Piebaldism P10721 (related)
H00023 Testicular cancer P10721 (marker)
H00255 Hypogonadotropic hypogonadism P11362 (related)
H00443 Osteoglophonic dysplasia (OD) P11362 (related)
H00458 Craniosynostosis P11362 (related)
P21802 (related)
H00516 Isolated orofacial clefts P11362 (related)
H01207 Trigonocephaly P11362 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00548 Brunner syndrome P21397 (related)
H00642 Lacrimo-auriculo-dento-digital syndrome (LADD) P21802 (related)
H00539 PTEN hamartoma tumor syndrome (PHTS) P31749 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00408 Type I diabetes mellitus Q04759 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)