| class name | count |
|---|---|
| rosids | 57 |
| asterids | 28 |
| class name | count |
|---|---|
| Fabaceae | 41 |
| Asteraceae | 18 |
| Apiaceae | 10 |
| Moraceae | 9 |
| Cannabaceae | 6 |
| Euphorbiaceae | 1 |
| 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
|
Corylifolinin
/ Isobavachalcone / 2',4,4'-Trihydroxy-3'-(3-methyl-2-butenyl)chalcone |
CHEMBL253467
|
C468754
|
8 / 22 / 21 |
|
|
|
C00007045
|
Isocordoin
|
CHEMBL460618
|
|
|||
|
C00007052
|
Derricin
|
CHEMBL455982
|
|
|||
|
C00007053
|
Derricidin
|
CHEMBL450771
|
2 / 1 / 1 |
|
||
|
C00007056
|
Licochalcone C
|
CHEMBL141207
|
1 / 0 / 0 |
|
||
|
C00007064
|
4-Hydroxyderricin
|
CHEMBL458094
|
C068243
|
17 / 27 / 26 |
|
|
|
C00007065
|
Xanthoangelol D
|
CHEMBL1711961
|
6 / 15 / 41 |
|
||
|
C00007066
|
Xanthoangelol E
|
CHEMBL1718454
|
10 / 21 / 44 |
|
||
|
C00007067
|
4-Hydroxycordoin
|
CHEMBL460400
|
1 / 0 / 0 |
|
||
|
C00007068
|
Broussochalcone B
|
CHEMBL464428
|
1 / 2 / 2 |
|
||
|
C00007070
|
Bavachalcone
|
|
||||
|
C00007078
|
Desmethylisoxanthohumol
|
CHEMBL2203298
|
|
|||
|
C00007081
|
Isoxanthohumol(Helichrysum)
|
|
||||
|
C00007083
|
2',4'-Dihydroxy-6'-methoxy-3'-prenylchalcone
|
|
||||
|
C00007085
|
Ovalichalcone
|
|
||||
|
C00007086
|
2',6'-Dihydroxy-4'-prenyloxychalcone
|
|
||||
|
C00007087
|
2'-Hydroxy-6'-methoxy-4'-prenyloxychalcone
|
|
||||
|
C00007089
|
Licochalcone D
|
CHEMBL1644932
|
|
|||
|
C00007091
|
Morachalcone A
|
CHEMBL465880
|
1 / 2 / 2 |
|
||
|
C00007095
|
Broussochalcone A
|
CHEMBL115452
|
C106525
|
2 / 2 / 2 |
|
|
|
C00007099
|
Xanthohumol
|
CHEMBL253896
|
6 / 0 / 1 |
|
||
|
C00007100
|
4'-O-Methylxanthohumol
|
CHEMBL466335
|
|
|||
|
C00007101
|
4,2',6'-Trihydroxy-4'-prenyloxychalcone
|
|
||||
|
C00007125
|
Xanthoangelol B
|
CHEMBL494082
|
13 / 11 / 5 |
|
||
|
C00007159
|
Xanthoangelol C
|
|
||||
|
C00014450
|
Psorachalcone A
|
CHEMBL428420
|
|
|||
|
C00014456
|
Licoagrochalcone A
/ 3-Prenyl-4,2',4'-trihydroxychalcone |
CHEMBL229885
|
2 / 2 / 2 |
|
||
|
C00014460
|
Xanthoangelol F
/ 3'-Geranyl-2',4-dihydroxy-4'-methoxychalcone |
CHEMBL1722838
|
8 / 6 / 6 |
|
||
|
C00014461
|
Xanthoangelol G
/ 3'-(3,7-Dimethyl-6-hydroxyocta-2,7-dienyl)-4,2'-dihydroxy-4'-methoxychalcone |
CHEMBL1823414
|
|
|||
|
C00014472
|
Xanthohumol D
/ 3'-(2-Hydroxy-3-methylbutyl-3-enyl)-4,2',4'-trihydroxy-6'-methoxychalcone |
CHEMBL479500
|
|
|||
|
C00014475
|
Xanthogalenol
/ 3'-Prenyl-4,2',6'-trihydroxy-4'-methoxychalcone |
CHEMBL466334
|
|
|||
|
C00014487
|
Licoagrochalcone C
/ 3-Prenyl-4,3',4'-trihydroxy-2-methoxychalcone |
|
||||
|
C00014491
|
Ramosismin
/ 3'-Prenyl-2,4,5,2',4'-pentahydroxychalcone |
|
||||
|
C00014492
|
3'-Prenyl-2',6',beta-trihydroxy-4'-methoxychalcone
|
|
||||
|
C00033900
|
Helichrysone A
|
|
||||
|
C00035575
|
Desmethylxanthohumol
|
CHEMBL466143
|
1 / 4 / 1 |
|
||
|
C00035796
|
5-Prenylbutein
|
CHEMBL253677
|
|
|||
|
C00036579
|
4-Hydroxyisocordoin
|
CHEMBL253467
|
8 / 22 / 21 |
|
||
|
C00040675
|
Xanthokeismin A
|
CHEMBL503569
|
|
|||
|
C00041964
|
Xanthoangelol J
|
CHEMBL491512
|
|
| 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 |
| 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 | 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)
|