Metabolite list (8)

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
C00002636 External link 512 Anisaldehyde
/ p-Anisaldehyde
CHEMBL161598
C024896
11 / 18 / 13 1 / 0
C00002683 External link 512 Vanillin
CHEMBL13883
18 / 8 / 9
C00029531 External link 512 Vanillic aldehyde
/ 4-Hydroxy-3-methoxybenzaldehyde
CHEMBL13883
C100058
18 / 8 / 9 33 / 1
C00036597 External link 512 5-Hydroxy-2-methoxy benzaldehyde
CHEMBL1988977
C00044431 External link 512 2-Hydroxy-5-methoxybenzaldehyde
C00044826 External link 512 Isovanillin
CHEMBL275563
C093382
7 / 8 / 4
C00047056 External link 512 Isovanillin
CHEMBL275563
C093382
7 / 8 / 4
C00049046 External link 512 Isovanillin
CHEMBL275563
C093382
7 / 8 / 4

Human Protein / Gene in interactions

29 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P00352 Retinal dehydrogenase 1 Enzyme C00002636 C00002683 C00029531 C00044826 C00047056 C00049046 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002683 C00029531 C00044826 C00047056 C00049046 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002636 C00044826 C00047056 C00049046 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002636 C00002683 C00029531 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00044826 C00047056 C00049046 0 / 0
P10275 Androgen receptor NR3C4 C00002636 C00002683 C00029531 3 / 4
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00044826 C00047056 C00049046 1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00044826 C00047056 C00049046 7 / 3
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002636 C00002683 C00029531 1 / 1
Q06278 Aldehyde oxidase Enzyme C00044826 C00047056 C00049046 0 / 1
O00519 Fatty-acid amide hydrolase 1 Enzyme C00002683 C00029531 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002683 C00029531 0 / 0
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00002683 C00029531 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00002683 C00029531 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002683 C00029531 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002683 C00029531 1 / 1
P78527 DNA-dependent protein kinase catalytic subunit Atypical serine/threonine protein kinase PIKK subfamily C00002683 C00029531 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00002683 C00029531 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002683 C00029531 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002683 C00029531 2 / 2
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002683 C00029531 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00002683 C00029531 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002683 C00029531 0 / 0
P03372 Estrogen receptor NR3A1 C00002636 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002636 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002636 5 / 3
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00002636 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00002636 3 / 1
P14679 Tyrosinase Oxidoreductase C00002636 4 / 2

34 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8989 TRPA1, ANKTM1, FEPS transient receptor potential cation channel, subfamily A, member 1 C00002636
1646 AKR1C2, AKR1C-pseudo, BABP, DD, DD2, DDH2, HAKRD, HBAB, MCDR2, SRXY8 aldo-keto reductase family 1, member C2 (EC:1.3.1.20 1.1.1.357) C00029531
759 CA1, CA-I, CAB, Car1 carbonic anhydrase I (EC:4.2.1.1) C00029531
760 CA2, CA-II, CAC, CAII, Car2 carbonic anhydrase II (EC:4.2.1.1) C00029531
1196 CLK2, hCLK2 CDC-like kinase 2 (EC:2.7.12.1) C00029531
1490 CTGF, CCN2, HCS24, IGFBP8, NOV2 connective tissue growth factor C00029531
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00029531
54541 DDIT4, Dig2, REDD-1, REDD1 DNA-damage-inducible transcript 4 C00029531
1789 DNMT3B, ICF, ICF1, M.HsaIIIB DNA (cytosine-5-)-methyltransferase 3 beta (EC:2.1.1.37) C00029531
1848 DUSP6, HH19, MKP3, PYST1 dual specificity phosphatase 6 (EC:3.1.3.16 3.1.3.48) C00029531
2263 FGFR2, BBDS, BEK, BFR-1, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25 fibroblast growth factor receptor 2 (EC:2.7.10.1) C00029531
2535 FZD2, Fz2, fz-2, fzE2, hFz2 frizzled family receptor 2 C00029531
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00029531
2730 GCLM, GLCLR glutamate-cysteine ligase, modifier subunit (EC:6.3.2.2) C00029531
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00029531
3251 HPRT1, HGPRT, HPRT hypoxanthine phosphoribosyltransferase 1 (EC:2.4.2.8) C00029531
3304 HSPA1B, HSP70-1B, HSP70-2 heat shock 70kDa protein 1B C00029531
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00029531
3638 INSIG1, CL-6, CL6 insulin induced gene 1 C00029531
3727 JUND, AP-1 jun D proto-oncogene C00029531
5605 MAP2K2, CFC4, MAPKK2, MEK2, MKK2, PRKMK2 mitogen-activated protein kinase kinase 2 (EC:2.7.12.2) C00029531
57787 MARK4, MARK4L, MARK4S, MARKL1, MARKL1L, PAR-1D MAP/microtubule affinity-regulating kinase 4 (EC:2.7.11.1) C00029531
4502 MT2A, MT2 metallothionein 2A C00029531
5514 PPP1R10, CAT53, FB19, PNUTS, PP1R10, R111, p99 protein phosphatase 1, regulatory subunit 10 C00029531
11046 SLC35D2, HFRC1, SQV7L, UGTrel8, hfrc solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2 C00029531
23657 SLC7A11, CCBR1, xCT solute carrier family 7 (anionic amino acid transporter light chain, xc- system), member 11 C00029531
7041 TGFB1I1, ARA55, HIC-5, HIC5, TSC-5 transforming growth factor beta 1 induced transcript 1 C00029531
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00029531
10626 TRIM16, EBBP tripartite motif containing 16 C00029531
7360 UGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379 UDP-glucose pyrophosphorylase 2 (EC:2.7.7.9) C00029531
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00029531
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00029531
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00029531
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00029531

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (29)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#119900 Digital clubbing, isolated congenital P15428
#615363 Estrogen resistance; estrr P03372
#613163 Gaba-transaminase deficiency P80404
#137800 Glioma susceptibility 1; glm1 P37231
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#174800 Mccune-albright syndrome; mas P63092
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#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
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#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
#278300 Xanthinuria, type i P47989

KEGG DISEASE (20)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (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)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00192 Xanthinuria P47989 (related)
Q06278 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008113 Liver Neoplasms C00029531