Plant Species


Cumulative plant class count

class name count
rosids 10

Cumulative family count

class name count
Fabaceae 6
Pandaceae 4

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (4)

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 External link 512 Bonducellin
/ (E)-7-Hydroxy-3-(4'-methoxybenzylidene)chroman-4-one
CHEMBL450675
CHEMBL1253830
8 / 25 / 23
C00020222 External link 512 Intricatin
/ 8-Methoxybonducellin
C00020609 External link 512 Intricatinol
CHEMBL233805
C061633
C00030225 External link 512 Eucomin
CHEMBL476776
7 / 20 / 19

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

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 DISEASE (23)

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)