KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (7)

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
C00002741 External link 512 Methyleugenol
/ 4-Allylveratrole
/ Eugenol methyl ether
CHEMBL108861
C005223
12 / 13 / 9 3 / 9
C00035487 External link 512 3,4-Dimethoxybenzyl alcohol
C042197
C00036577 External link 512 4-Hydroxy-3,5-dimethoxybenzyl alcohol
C00042104 External link 512 3,4-Dimethoxy-5-hydroxy-beta-phenethylamine
CHEMBL1187491
C00042105 External link 512 3,4-Dimethoxyphenethylamine
CHEMBL26019
6 / 8 / 40
C00042109 External link 512 3,5-Dimethoxytyramine
C00042775 External link 512 N-Methyl-3,4-dimethoxyphenethylamine
CHEMBL1404381
5 / 8 / 7

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q92830 Histone acetyltransferase KAT2A Enzyme C00002741 C00042105 C00042775 0 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00042105 C00042775 1 / 4
P04150 Glucocorticoid receptor NR3C1 C00002741 0 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00042105 7 / 37
P10828 Thyroid hormone receptor beta NR1A2 C00002741 3 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002741 0 / 0
P39748 Flap endonuclease 1 Enzyme C00042775 0 / 0
P06746 DNA polymerase beta Enzyme C00042775 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002741 2 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00042775 7 / 3
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002741 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002741 5 / 3
Q96RI1 Bile acid receptor NR1H4 C00002741 0 / 0
Q16853 Membrane primary amine oxidase Enzyme C00042105 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002741 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00042105 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002741 0 / 0
P10275 Androgen receptor NR3C4 C00002741 3 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00002741 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00042105 0 / 0

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2938 GSTA1, GST2, GSTA1-1, GTH1 glutathione S-transferase alpha 1 (EC:2.5.1.18) C00002741
2944 GSTM1, GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1, H-B, MU, MU-1 glutathione S-transferase mu 1 (EC:2.5.1.18) C00002741
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00002741

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (28)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#208900 Ataxia-telangiectasia; at Q13315
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P84022
#133239 Esophageal cancer P04637
#137800 Glioma susceptibility 1; glm1 P37231
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#174800 Mccune-albright syndrome; mas P63092
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#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
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#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

KEGG DISEASE (51)

KEGG name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (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)
P37231 (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)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)

Diseases related to CTD interactions

9 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000707 Anaphylaxis C00002741
D001943 Breast Neoplasms C00002741
D003328 Coronary Thrombosis C00002741
D006529 Hepatomegaly C00002741
D006930 Hyperalgesia C00002741
D008113 Liver Neoplasms C00002741
D008114 Liver Neoplasms, Experimental C00002741
D008325 Mammary Neoplasms, Experimental C00002741
D009374 Neoplasms, Experimental C00002741