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)
|