class name | count |
---|---|
rosids | 10 |
class name | count |
---|---|
Fabaceae | 6 |
Pandaceae | 4 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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 |
---|---|---|---|---|---|---|
C00020039
![]() |
Bonducellin
/ (E)-7-Hydroxy-3-(4'-methoxybenzylidene)chroman-4-one |
CHEMBL450675
CHEMBL1253830 |
8 / 25 / 23 |
![]() |
||
C00020222
![]() |
Intricatin
/ 8-Methoxybonducellin |
![]() |
||||
C00020609
![]() |
Intricatinol
|
CHEMBL233805
|
C061633
|
![]() |
||
C00030225
![]() |
Eucomin
|
CHEMBL476776
|
7 / 20 / 19 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P21802 | Fibroblast growth factor receptor 2 | TK tyrosine-protein kinase TLK subfamily | C00020039 C00030225 | 9 / 3 |
P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00020039 C00030225 | 1 / 8 |
P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00020039 C00030225 | 0 / 0 |
P35968 | Vascular endothelial growth factor receptor 2 | Vegfr | C00020039 C00030225 | 1 / 0 |
P10721 | Mast/stem cell growth factor receptor Kit | Pdgfr | C00020039 C00030225 | 4 / 3 |
P11362 | Fibroblast growth factor receptor 1 | Fgfr | C00020039 C00030225 | 4 / 5 |
P08581 | Hepatocyte growth factor receptor | TK tyrosine-protein kinase MET subfamily | C00020039 C00030225 | 2 / 3 |
O14746 | Telomerase reverse transcriptase | Enzyme | C00020039 | 5 / 5 |
OMIM | preferred title | UniProt |
---|---|---|
#207410 | Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 |
P21802
|
#101200 | Apert syndrome |
P21802
|
#609135 | Aplastic anemia |
O14746
|
#123790 | Beare-stevenson cutis gyrata syndrome; bstvs |
P21802
|
#614592 | Bent bone dysplasia syndrome; bbds |
P21802
|
#123500 | Crouzon syndrome |
P21802
|
#613989 | Dyskeratosis congenita, autosomal dominant, 2; dkca2 |
O14746
|
#606764 | Gastrointestinal stromal tumor; gist |
P10721
|
#602089 | Hemangioma, capillary infantile |
P35968
|
#114550 | Hepatocellular carcinoma |
P08581
|
#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
|
#211980 | Lung cancer |
P00533
|
#615134 | Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 |
O14746
|
#166250 | Osteoglophonic dysplasia; ogd |
P11362
|
#101600 | Pfeiffer syndrome |
P11362
P21802 |
#172800 | Piebald trait; pbt |
P10721
|
#614742 | Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 |
O14746
|
#178500 | Pulmonary fibrosis, idiopathic; ipf |
O14746
|
#605074 | Renal cell carcinoma, papillary, 1; rccp1 |
P08581
|
#609579 | Scaphocephaly, maxillary retrusion, and mental retardation |
P21802
|
#273300 | Testicular germ cell tumor; tgct |
P10721
|
#190440 | Trigonocephaly 1; trigno1 |
P11362
|
KEGG | name | UniProt |
---|---|---|
H00764 | Cri du chat syndrome |
O14746
(related)
|
H01132 | Aplastic anemia (AA) |
O14746
(related)
|
H01299 | Idiopathic pulmonary fibrosis |
O14746
(related)
|
H00022 | Bladder cancer |
O14746
(marker)
P00533 (related) |
H00024 | Prostate cancer |
O14746
(marker)
|
H00016 | Oral cancer |
P00533
(related)
P00533 (marker) |
H00017 | Esophageal cancer |
P00533
(related)
|
H00018 | Gastric cancer |
P00533
(related)
P08581 (related) P21802 (related) |
H00028 | Choriocarcinoma |
P00533
(related)
|
H00030 | Cervical cancer |
P00533
(related)
|
H00042 | Glioma |
P00533
(related)
P00533 (marker) |
H00055 | Laryngeal cancer |
P00533
(related)
P00533 (marker) |
H00021 | Renal cell carcinoma |
P08581
(related)
|
H00046 | Cholangiocarcinoma |
P08581
(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)
|
H00642 | Lacrimo-auriculo-dento-digital syndrome (LADD) |
P21802
(related)
|