| class name | count |
|---|---|
| rosids | 25 |
| Liliopsida | 16 |
| asterids | 13 |
| eudicotyledons | 2 |
| Euphyllophyta | 1 |
| Embryophyta | 1 |
| class name | count |
|---|---|
| Anacardiaceae | 17 |
| Cyperaceae | 15 |
| Asteraceae | 11 |
| Fabaceae | 5 |
| Plantaginaceae | 2 |
| Plumbaginaceae | 2 |
| Simaroubaceae | 1 |
| Asparagaceae | 1 |
| Passifloraceae | 1 |
| Aspleniaceae | 1 |
| Funariaceae | 1 |
| Moraceae | 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 |
|---|---|---|---|---|---|---|
|
C00008024
|
Hispidol
|
CHEMBL426110
CHEMBL502446 |
2 / 4 / 2 |
|
||
|
C00008025
|
4,6,4'-Trihydroxyaurone
|
CHEMBL201626
CHEMBL466981 |
2 / 4 / 2 |
|
||
|
C00008026
|
Sulfuretin
/ Sulphuretin / 6,3',4'-Trihydroxyaurone |
CHEMBL490355
CHEMBL513487 |
C054989
|
42 / 37 / 34 |
|
|
|
C00008027
|
Aureusidin
|
CHEMBL593229
|
|
|||
|
C00008028
|
Rengasin
|
|
||||
|
C00008029
|
Maritimetin
|
|
||||
|
C00008030
|
Leptosidin
|
|
||||
|
C00008031
|
Bracteatin
|
|
||||
|
C00008032
|
6,3',4'-Trihydroxy-4-methoxy-5-methylaurone
|
|
||||
|
C00014649
|
Broussoaurone A
/ 2-[(3,4-Dihydroxyphenyl)methylene]-6-hydroxy-5-(3-methyl-2-butenyl)-3(2H)-benzofuranone |
CHEMBL463019
|
|
|||
|
C00014650
|
Licoagroaurone
/ (2Z)-2-[(3,4-Dihydroxyphenyl)methylene]-6-hydroxy-7-(3-methyl-2-butenyl)-3(2H)-benzofuranone |
|
||||
|
C00014652
|
Helmon
/ 4,7,4',6-Tetrahydroxyaurone |
|
||||
|
C00014653
|
4,6,3',4'-Tetrahydroxy-5-methylaurone
|
|
||||
|
C00014654
|
4,6,3',4'-Tetrahydroxy-7-methylaurone
|
|
||||
|
C00014655
|
6,3',4'-Trihydroxy-4-methoxy-7-methylaurone
|
|
||||
|
C00014656
|
6,3'-Dihydroxy-4,4'-dimethoxy-5-methylaurone
|
|
||||
|
C00044469
|
6,4'-Dihydroxy-3'-methoxyaurone
|
CHEMBL446827
|
28 / 32 / 55 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00008026 C00044469 | 2 / 1 |
| Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00008026 C00044469 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00008026 C00044469 | 2 / 5 |
| Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00008026 C00044469 | 0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00008026 C00044469 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00008026 C00044469 | 1 / 1 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00008026 C00044469 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00008026 C00044469 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00008026 C00044469 | 4 / 3 |
| P15559 | NAD(P)H dehydrogenase [quinone] 1 | Enzyme | C00008024 C00008025 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00008026 C00044469 | 0 / 0 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00008026 C00044469 | 1 / 0 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00008026 C00044469 | 0 / 0 |
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00008026 C00044469 | 1 / 1 |
| P39748 | Flap endonuclease 1 | Enzyme | C00008026 C00044469 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00008026 C00044469 | 0 / 0 |
| P14679 | Tyrosinase | Oxidoreductase | C00008024 C00008025 | 4 / 2 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00008026 C00044469 | 7 / 3 |
| P11308 | Transcriptional regulator ERG | Unclassified protein | C00008026 C00044469 | 1 / 2 |
| P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00008026 C00044469 | 4 / 2 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00008026 C00044469 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00008026 C00044469 | 1 / 2 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00008026 | 1 / 1 |
| P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00008026 | 0 / 0 |
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00008026 | 3 / 1 |
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00044469 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00044469 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00044469 | 0 / 0 |
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00008026 | 0 / 0 |
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00008026 | 0 / 0 |
| Q99816 | Tumor susceptibility gene 101 protein | Unclassified protein | C00044469 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00008026 | 2 / 0 |
| P10696 | Alkaline phosphatase, placental-like | Enzyme | C00008026 | 0 / 1 |
| P08253 | 72 kDa type IV collagenase | M10A | C00008026 | 1 / 3 |
| P47901 | Vasopressin V1b receptor | Vasopressin and oxytocin receptor | C00008026 | 0 / 0 |
| Q8WXD0 | Relaxin receptor 2 | Relaxin receptor | C00008026 | 1 / 1 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00008026 | 2 / 3 |
| Q9HBX9 | Relaxin receptor 1 | Relaxin receptor | C00008026 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00008026 | 0 / 0 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00008026 | 3 / 1 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00008026 | 0 / 0 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00044469 | 0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00044469 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00008026 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00044469 | 1 / 1 |
| O00487 | 26S proteasome non-ATPase regulatory subunit 14 | Enzyme | C00008026 | 0 / 0 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00008026 | 0 / 0 |
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00008026 | 0 / 1 |
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00008026 | 1 / 4 |
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00008026 | 0 / 0 |
| Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00008026 | 0 / 0 |
| P04637 | Cellular tumor antigen p53 | Transcription Factor | C00044469 | 7 / 37 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
| #103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
| #203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
| #606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
| #614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
| #114480 | Breast cancer |
P38398
|
| #604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
| #114500 | Colorectal cancer; crc |
P84022
Q14191 |
| #219050 | Cryptorchidism, unilateral or bilateral |
Q8WXD0
|
| #133239 | Esophageal cancer |
P04637
|
| #612219 | Ewing sarcoma; es |
P11308
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #146300 | Hypophosphatasia, adult |
P05186
|
| #241510 | Hypophosphatasia, childhood |
P05186
|
| #241500 | Hypophosphatasia, infantile |
P05186
|
| #151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #211980 | Lung cancer |
P04637
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #167000 | Ovarian cancer |
P38398
|
| #614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
| #260500 | Papilloma of choroid plexus; cpp |
P04637
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
| #601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
| #103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
| #603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
| #612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
| #601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| #277700 | Werner syndrome; wrn |
Q14191
|
| #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)
|
| H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
| H00004 | Chronic myeloid leukemia (CML) |
P04637
(related)
Q01196 (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)
|
| 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) |
| H00022 | Bladder cancer |
P04637
(related)
|
| H00025 | Penile cancer |
P04637
(related)
P04637 (marker) P08253 (related) |
| H00026 | Endometrial Cancer |
P04637
(related)
|
| H00027 | Ovarian cancer |
P04637
(related)
P38398 (related) |
| H00028 | Choriocarcinoma |
P04637
(related)
P08253 (related) |
| H00029 | Vulvar cancer |
P04637
(related)
|
| H00031 | Breast cancer |
P04637
(related)
P38398 (related) |
| H00032 | Thyroid cancer |
P04637
(related)
|
| H00036 | Osteosarcoma |
P04637
(related)
|
| H00038 | Malignant melanoma |
P04637
(related)
P14679 (marker) |
| 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)
|
| H00213 | Hypophosphatasia |
P05186
(related)
|
| H00472 | Torg-Winchester syndrome |
P08253
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00023 | Testicular cancer |
P10696
(marker)
|
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H00024 | Prostate cancer |
P11308
(related)
|
| H00035 | Ewing's sarcoma |
P11308
(related)
|
| H00342 | Tuberculosis |
P11473
(related)
|
| H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
| H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
| H00168 | Oculocutaneous albinism (OCA) |
P14679
(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) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
| H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
| H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00296 | Defects in RecQ helicases |
Q14191
(related)
|
| H00609 | 46,XY disorders of sex development (Other) |
Q8WXD0
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|