Metabolite list (54)

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
C00006923 External link 512 Glypallichalcone
/ 4-Hydroxy-2,4'-dimethoxychalcone
C079973
C00006929 External link 512 Isoliquiritigenin 4,4'-dimethyl ether
CHEMBL229907
18 / 36 / 28
C00006936 External link 512 Flavokawin B
CHEMBL104255
19 / 31 / 55
C00006937 External link 512 Tepanone
C00006939 External link 512 2,4-Dihydroxy-6,4'-dimethoxychalcone
C00006946 External link 512 2',4'-Dihydroxy-3,4-dimethoxychalcone
CHEMBL573524
19 / 38 / 59
C00006950 External link 512 Kukulkanin A
C061638
C00006955 External link 512 Gymnogrammene
C00006956 External link 512 4,4'-Dihydroxy-2',6'-dimethoxychalcone
CHEMBL449907
C00006957 External link 512 Flavokawain C
CHEMBL251958
C00006958 External link 512 Flavokawin A
/ 2'-Hydroxy-4,4',6'-trimethoxychalcone
CHEMBL243829
3 / 3 / 0
C00006959 External link 512 Pashanone
C00006960 External link 512 2',4'-Dihydroxy-3',6'-dimethoxychalcone
C00006961 External link 512 2',3'-Dihydroxy-4',6'-dimethoxychalcone
CHEMBL1446527
13 / 17 / 11
C00006962 External link 512 Helilandin B
C00006963 External link 512 2'-Hydroxy-3',4',6'-trimethoxychalcone
C00006964 External link 512 2',3',4',6'-Tetramethoxychalcone
C00006965 External link 512 Cerasin
CHEMBL601679
C00006966 External link 512 Cerasidin
C00006967 External link 512 2',4'-Dihydroxy-2,3',6'-trimethoxychalcone
C00006971 External link 512 Okanin 3,4,3',4'-tetramethyl ether
CHEMBL316850
CHEMBL1702432
11 / 8 / 9
C00006976 External link 512 3,2'-Dihydroxy-4,4',6'-trimethoxychalcone
CHEMBL571087
15 / 19 / 52
C00006977 External link 512 2'-Hydroxy-3,4,4',6'-tetramethoxychalcone
CHEMBL243830
3 / 3 / 0
C00006979 External link 512 4,6'-Dihydroxy-2',3',4'-trimethoxychalcone
CHEMBL2208192
C00006980 External link 512 4,2'-Dihydroxy-3',4',6'-trimethoxychalcone
C00006981 External link 512 6'-Hydroxy-4,2',3',4'-tetramethoxychalcone
CHEMBL2208193
1 / 5 / 3
C00006982 External link 512 Pedicin
/ 2',5'-Dihydroxy-3',4',6'-trimethoxychalcone
CHEMBL481972
C00006983 External link 512 Isodidymocarpin
CHEMBL505666
C00006984 External link 512 3'-Hydroxy-2',4',5',6'-tetramethoxychalcone
C00006985 External link 512 Kanakugiol
C00006986 External link 512 Pedicellin
CHEMBL1998453
C00006987 External link 512 Rubone
C00006988 External link 512 2'-Hydroxy-3,4,5,4',6'-pentamethoxychalcone
CHEMBL571877
1 / 2 / 0
C00006989 External link 512 6'-Hydroxy-3,4,2',3',4'-pentamethoxychalcone
CHEMBL458376
C00006990 External link 512 2',5'-Dihydroxy-4,3',4',6'-tetramethoxychalcone
C00014421 External link 512 Heliannone A
/ 2',4-Dihydroxy-3',4'-dimethoxychalcone
C00014423 External link 512 2'-Hydroxy-2,4',6'-trimethoxychalcone
CHEMBL258497
1 / 2 / 0
C00014424 External link 512 2',4'-Dihydroxy-4,6'-dimethoxychalcone
CHEMBL494264
C00014425 External link 512 3'-Bromo-6'-hydroxy-2',4,4'-trimethoxychalcone
C00014426 External link 512 4'-Hydroxy-2',4,6'-trimethoxychalcone
CHEMBL1514861
2 / 3 / 4
C00014428 External link 512 Crotaoprostrin
/ 2'-Hydroxy-3,4,5-methoxychalcone
CHEMBL521653
16 / 23 / 18
C00014430 External link 512 2'-Hydroxy-2,3,4',6'-tetramethoxychalcone
CHEMBL1254091
1 / 5 / 5
C00014433 External link 512 4,3'-Hydroxy-2',4',5',6'-methoxychalcone
C00014434 External link 512 Hamilcone
/ 3,4,6'-Trihydroxy-2',3',4'-trimethoxychalcone
CHEMBL465364
C00014435 External link 512 2'-Hydroxy-3',4',6',3,4-pentamethoxychalcone
C00014436 External link 512 2,3,4,2',4',6'-Hexamethoxychalcone
CHEMBL595815
C00032628 External link 512 2'-Hydroxy-3,4,3',4',6'-pentamethoxychalcone
C00036451 External link 512 2',3'-Dihydroxy-4',6'-dimethoxychalcone
CHEMBL1446527
13 / 17 / 11
C00036493 External link 512 2'-Hydroxy-4,4',6'-trimethoxychalcone
CHEMBL243829
3 / 3 / 0
C00037157 External link 512 Flavokavin A
/ Flavokawain A
CHEMBL243829
3 / 3 / 0
C00044793 External link 512 Guieranone A
CHEMBL477526
C00045544 External link 512 2'-Hydroxy-4',6'-dimethoxychalcone
CHEMBL104255
19 / 31 / 55
C00048940 External link 512 2'-Hydroxy-4',5',6'-trimethoxychalcone
C00048941 External link 512 2'-Hydroxy-4',6'-dimethoxychalcone
CHEMBL104255
19 / 31 / 55

Human Protein / Gene in interactions

51 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00006929 C00006936 C00006946 C00006958 C00006977 C00006988 C00014423 C00036493 C00037157 C00045544 C00048941 2 / 0
P11473 Vitamin D3 receptor NR1I1 C00006936 C00006946 C00006961 C00006971 C00006976 C00014426 C00014428 C00036451 C00045544 C00048941 2 / 3
P10636 Microtubule-associated protein tau Unclassified protein C00006929 C00006936 C00006946 C00006961 C00006976 C00014428 C00036451 C00045544 C00048941 4 / 3
O75496 Geminin Unclassified protein C00006929 C00006936 C00006961 C00006971 C00014428 C00036451 C00045544 C00048941 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00006936 C00006961 C00006971 C00014428 C00036451 C00045544 C00048941 0 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00006929 C00006946 C00006958 C00006977 C00036493 C00037157 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00006929 C00006936 C00006946 C00006976 C00045544 C00048941 1 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00006929 C00006936 C00006961 C00036451 C00045544 C00048941 7 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00006929 C00006936 C00006946 C00006976 C00045544 C00048941 0 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00006936 C00006961 C00014428 C00036451 C00045544 C00048941 0 / 0
P08183 Multidrug resistance protein 1 drug C00006929 C00006946 C00006958 C00006977 C00036493 C00037157 1 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00006936 C00006946 C00014428 C00045544 C00048941 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00006929 C00006961 C00006971 C00014428 C00036451 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00006929 C00006936 C00014428 C00045544 C00048941 0 / 0
Q99700 Ataxin-2 Unclassified protein C00006936 C00006961 C00036451 C00045544 C00048941 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00006936 C00006971 C00014428 C00045544 C00048941 1 / 0
Q9UNA4 DNA polymerase iota Enzyme C00006929 C00006961 C00006971 C00014428 C00036451 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00006936 C00006946 C00006976 C00045544 C00048941 7 / 37
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00006936 C00014428 C00045544 C00048941 2 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00006936 C00006976 C00045544 C00048941 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00006946 C00006976 C00014428 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00006946 C00006976 C00014426 1 / 1
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00006936 C00045544 C00048941 1 / 4
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00006929 C00006961 C00036451 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00006961 C00014428 C00036451 0 / 0
O00255 Menin Unclassified protein C00006929 C00006946 C00006976 2 / 5
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00006936 C00045544 C00048941 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00006929 C00006946 C00006976 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00006936 C00045544 C00048941 3 / 3
Q16637 Survival motor neuron protein Unclassified protein C00006929 C00006946 4 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00006946 C00006981 5 / 3
P02545 Prelamin-A/C Unclassified protein C00006929 C00014428 11 / 10
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00006961 C00036451 1 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00006946 C00006976 2 / 2
Q9Y253 DNA polymerase eta Enzyme C00006961 C00036451 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00006946 C00006976 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00006946 2 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00006971 0 / 0
P37840 Alpha-synuclein Unclassified protein C00006971 4 / 2
P04062 Glucosylceramidase Enzyme C00006946 6 / 4
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00006929 1 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00006976 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00006929 2 / 2
O14746 Telomerase reverse transcriptase Enzyme C00014430 5 / 5
B2RXH2 Lysine-specific demethylase 4E Enzyme C00006976 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00014428 0 / 0
P39748 Flap endonuclease 1 Enzyme C00006971 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00014428 2 / 2
O15296 Arachidonate 15-lipoxygenase B Enzyme C00006976 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00006971 0 / 3
P14555 Phospholipase A2, membrane associated Enzyme C00006971 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (78)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#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
#609135 Aplastic anemia O14746
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#208900 Ataxia-telangiectasia; at Q13315
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#614490 Blood group, junior system; jr Q9UNQ0
%606641 Body mass index; bmi P37231
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
P84022
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#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
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#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
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#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 P04062
P37840
#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
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#275210 Restrictive dermopathy, lethal P02545
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (91)

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)
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
P04637 (related)
H00024 Prostate cancer O14746 (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)
P37231 (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)
H00066 Lewy body dementia (LBD) P04062 (related)
P37840 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (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)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer 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)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00057 Parkinson's disease (PD) 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)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)