Metabolite list (16)

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
C00000660 External link 512 Feruloyl tyramine
CHEMBL206555
CHEMBL451720
C074004
1 / 4 / 2
C00000661 External link 512 N-trans-Sinapoyltyramine
CHEMBL226587
C00000662 External link 512 Caffeoyl tyramine
CHEMBL206646
1 / 4 / 2
C00025324 External link 512 N-cis-Feruloyltyramine
/ cis-N-Feruloyltyramine
CHEMBL206555
CHEMBL451720
1 / 4 / 2
C00025334 External link 512 trans-Feruloyltyramine
/ N-trans-Feruloyltyramine
/ trans-N-Feruloyltyramine
CHEMBL206555
CHEMBL451720
1 / 4 / 2
C00027156 External link 512 N-trans-Cinnamoyltyramine
CHEMBL417389
C00027418 External link 512 N-cis-Coumaroyltyramine
/ N-p-cis-Coumaroyltyramine
/ cis-N-p-Coumaroyltyramine
CHEMBL64286
C00027419 External link 512 Tuberosine A
/ N-cis-Feruloyldopamine
C00027445 External link 512 Tuberosine B
/ trans-N-Feruloyldopamine
/ N-trans-Feruloyldopamine
CHEMBL202844
1 / 4 / 2
C00028801 External link 512 Paprazine
/ N-p-Coumaroyl-tyramine
/ trans-N-(p-Coumaroyl)tyramine
CHEMBL64286
C00034085 External link 512 N-p-Coumaroyltyramine
CHEMBL64286
C00035142 External link 512 N-trans-Feruloyl tyramine
CHEMBL206555
CHEMBL451720
1 / 4 / 2
C00035344 External link 512 N-cis-Feruloyloctopamine
CHEMBL465182
CHEMBL1802149
CHEMBL2337114
C00040542 External link 512 trans-N-feruloyl-3-O-methyldopamine
CHEMBL226588
C00041207 External link 512 Terrestriamide
C00047162 External link 512 Ailanthamide
CHEMBL556469

Human Protein / Gene in interactions

1 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14679 Tyrosinase Oxidoreductase C00000660 C00000662 C00025324 C00025334 C00027445 C00035142 4 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679

KEGG DISEASE (2)

KEGG name UniProt
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)