class name | count |
---|---|
rosids | 19 |
asterids | 19 |
class name | count |
---|---|
Apiaceae | 18 |
Moraceae | 9 |
Rutaceae | 8 |
Fabaceae | 2 |
Goodeniaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Furanocoumarins | 3 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Furanocoumarins | C09276 | C00000584 |
Furanocoumarins | C09210 | C00002459 |
Furanocoumarins | C09278 | C00002485 |
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 |
---|---|---|---|---|---|---|
C00000584
![]() |
(+)-Marmesin
|
CHEMBL442813
CHEMBL1464240 |
C001684
|
12 / 24 / 49 |
![]() |
|
C00002459
![]() |
Columbianetin
|
CHEMBL201152
|
7 / 12 / 8 |
![]() |
||
C00002466
![]() |
Decursinol
|
CHEMBL481657
|
4 / 3 / 0 |
![]() |
||
C00002485
![]() |
Nodakenetin
|
CHEMBL442813
CHEMBL1464240 |
12 / 24 / 49 |
![]() |
||
C00019918
![]() |
Smyrindiol
/ Smirindiol / (+)-3'-Hydroxymarmesin / (2'S,3'R)-3'-Hydroxymarmesin / (+)-(2S',3'R)-3-Hydroxymarmesin |
![]() |
||||
C00029297
![]() |
Columbianetin
/ (+)-Columbianetin |
CHEMBL201152
|
7 / 12 / 8 |
![]() |
||
C00035226
![]() |
4',5'-Dihydropsoralen
|
C005771
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P56817 | Beta-secretase 1 | A1A | C00000584 C00002459 C00002466 C00002485 C00029297 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00000584 C00002459 C00002485 C00029297 | 2 / 2 |
P22303 | Acetylcholinesterase | Hydrolase | C00000584 C00002466 C00002485 | 1 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00000584 C00002466 C00002485 | 0 / 0 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00000584 C00002485 | 2 / 2 |
P04637 | Cellular tumor antigen p53 | Transcription Factor | C00000584 C00002485 | 7 / 37 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00000584 C00002485 | 0 / 3 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00000584 C00002485 | 4 / 2 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00002459 C00029297 | 7 / 3 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002459 C00029297 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00000584 C00002485 | 1 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002459 C00029297 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00000584 C00002485 | 1 / 1 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002459 C00029297 | 1 / 1 |
P04062 | Glucosylceramidase | Enzyme | C00000584 C00002485 | 6 / 4 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00000584 C00002485 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002459 C00029297 | 2 / 2 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002466 | 2 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#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
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#133239 | Esophageal cancer |
P04637
|
#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
|
#232300 | Glycogen storage disease ii |
P10253
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#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
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#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
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#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
|
#275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00066 | Lewy body dementia (LBD) |
P04062
(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)
|
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) |
H00026 | Endometrial Cancer |
P04637
(related)
|
H00027 | Ovarian cancer |
P04637
(related)
P38398 (related) |
H00028 | Choriocarcinoma |
P04637
(related)
|
H00029 | Vulvar cancer |
P04637
(related)
|
H00031 | Breast cancer |
P04637
(related)
P38398 (related) |
H00032 | Thyroid cancer |
P04637
(related)
|
H00033 | Adrenal carcinoma |
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)
|
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)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(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)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|