Plant Species


Cumulative plant class count

class name count
asterids 15
Liliopsida 11
rosids 3

Cumulative family count

class name count
Primulaceae 15
Iridaceae 11
Connaraceae 2
Oxalidaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (15)

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
C00002822 External link 512 Embelin
CHEMBL221137
C010945
29 / 32 / 60
C00002842 External link 512 5-O-Methylembelin
CHEMBL471270
C061025
C00002860 External link 512 Rapanone
CHEMBL462801
C054611
2 / 4 / 2
C00032649 External link 512 Irisoquin B
/ 3-Hydroxydihydroirisquinone
C00032650 External link 512 3-Hydroxyirisquinone
/ 5-Hydroxyirisquinone
C00032790 External link 512 Bungeiquinone
C00032907 External link 512 Dihydrobungeiquinone
C00037310 External link 512 Irisoquin
CHEMBL1975424
C047549
C00037311 External link 512 Irisoquin A
C00037312 External link 512 Irisoquin C
C00037313 External link 512 Irisoquin D
C00037314 External link 512 Irisoquin E
C00037315 External link 512 Irisoquin F
C00043214 External link 512 5-O-Ethylembelin
CHEMBL463108
C00049217 External link 512 Maesanin
C064887

Human Protein / Gene in interactions

29 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002822 C00002860 0 / 0
P00734 Prothrombin S1A C00002822 C00002860 4 / 2
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002822 3 / 3
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002822 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002822 0 / 1
P11473 Vitamin D3 receptor NR1I1 C00002822 2 / 3
P14416 D(2) dopamine receptor Dopamine receptor C00002822 2 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002822 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002822 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002822 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002822 1 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002822 2 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002822 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002822 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00002822 7 / 37
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002822 2 / 2
P16050 Arachidonate 15-lipoxygenase Enzyme C00002822 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002822 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002822 0 / 1
P98170 E3 ubiquitin-protein ligase XIAP Other cytosolic protein C00002822 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00002822 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002822 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002822 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002822 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00002822 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002822 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002822 1 / 1
O00255 Menin Unclassified protein C00002822 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002822 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (32)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103780 Alcohol dependence P14416
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114500 Colorectal cancer; crc P18054
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#300635 Lymphoproliferative syndrome, x-linked, 2; xlp2 P98170
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#159900 Myoclonic dystonia P14416
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601367 Stroke, ischemic P00734
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (60)

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)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (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)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00107 Other well-defined immunodeficiency syndromes P98170 (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)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)