Species

KNApSAcK Entry

Organism name Aganosma caryophyllata
Genus
Family
Kingdom

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
KCF-S
cluster
phytochemical
cluster
figure
C00005413 External link 512 Rutin
/ Birutan
/ 3-Rutinosylquercetin
/ Quercetin 3-O-rutinoside
/ (+)-Quercetin 3-O-rutinoside
/ Quercetin 3-O-beta-rutinoside
/ (+)-Quercetin 3-O-beta-rutinoside
/ 3,3',4',5,7-Pentahydroxyflavone 3-rutinoside
/ Quercetin 3-O-alpha-L-rhamnopyranosyl-(1->6)-beta-D-glucopyranoside
CHEMBL32579
CHEMBL310754
CHEMBL182108
CHEMBL226335
CHEMBL502782
CHEMBL1436093
CHEMBL1532989
D012431
25 / 18 / 16 29 / 8 No. 1 No. 15
C00005373 External link 512 Hirsutrin
/ Isoquercetin
/ Isoquercetrin
/ (-)-Isoquercetrin
/ Quercetin 3-glucoside
/ Quercetin 3-O-beta-D-glucoside
/ Quercetin-3-O-beta-D-glucopyranoside
/ Quercetin 3-O-beta-D-glucopyranoside
/ (-)-Quercetin-3-O-beta-D-glucopyranoside
CHEMBL33027
CHEMBL309323
CHEMBL250450
CHEMBL251254
CHEMBL457304
CHEMBL1098724
CHEMBL2337335
CHEMBL2337336
38 / 43 / 34 No. 2 No. 15
C00005372 External link 512 Hyperin
/ Hyperoside
/ Quercetin 3-O-galactoside
/ Quercetin 3-O-beta-D-galactoside
/ Quercetin 3-beta-galactopyranoside
/ Quercetin 3-O-beta-D-galactopyranoside
CHEMBL33027
CHEMBL309323
CHEMBL250450
CHEMBL251254
CHEMBL457304
CHEMBL1098724
CHEMBL2337335
CHEMBL2337336
C021304
38 / 43 / 34 4 / 0 No. 2 No. 15
C00005374 External link 512 Quercetin
CHEMBL82242
CHEMBL479232
CHEMBL1437696
C012526
14 / 2 / 2 2 / 1 No. 2 No. 15
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00029633 External link 512 Ursolic acid
/ Acetylursolic acid
CHEMBL55086
CHEMBL410525
4 / 2 / 2 No. 177
C00002682 External link 512 Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid
CHEMBL120568
D014641
5 / 3 / 3 5 / 0 No. 1073
C00002743 External link 512 Ferulic acid
/ 3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid
CHEMBL32749
C004999
110 / 52 / 40 16 / 6 No. 1366 No. 6

Human Protein / Gene in interactions

162 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005372 C00005373 C00005374 C00005413 C00029633 0 / 0
P06746 DNA polymerase beta Enzyme C00003672 C00005372 C00005373 C00005413 C00029633 0 / 0
P14679 Tyrosinase Oxidoreductase C00002743 C00003672 C00005372 C00005373 C00005413 4 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00002743 C00005372 C00005373 C00005374 C00005413 1 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002743 C00005372 C00005373 C00005374 C00005413 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002743 C00005372 C00005373 C00005413 0 / 0
P15121 Aldose reductase Enzyme C00002682 C00005372 C00005373 C00005374 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00002743 C00005372 C00005373 C00005413 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00005372 C00005373 C00005374 C00005413 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002682 C00005372 C00005373 C00005374 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002743 C00005372 C00005373 C00005413 0 / 3
P03372 Estrogen receptor NR3A1 C00002682 C00002743 C00003672 C00005413 1 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00005372 C00005373 C00005374 0 / 0
P07237 Protein disulfide-isomerase Enzyme C00005372 C00005373 C00005374 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00005372 C00005373 C00005413 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002743 C00003672 C00005413 0 / 1
P41145 Kappa-type opioid receptor Opioid receptor C00002743 C00005372 C00005373 0 / 0
P39748 Flap endonuclease 1 Enzyme C00005372 C00005373 C00005374 0 / 0
O75496 Geminin Unclassified protein C00002743 C00005372 C00005373 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00005372 C00005373 C00005413 1 / 1
P35372 Mu-type opioid receptor Opioid receptor C00002743 C00005372 C00005373 0 / 0
P41143 Delta-type opioid receptor Opioid receptor C00002743 C00005372 C00005373 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00005372 C00005373 C00005413 4 / 3
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00005372 C00005373 C00005413 2 / 0
Q9Y253 DNA polymerase eta Enzyme C00005372 C00005373 C00005374 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00005372 C00005373 C00005413 0 / 0
Q9NPH5 NADPH oxidase 4 Enzyme C00005372 C00005373 0 / 0
P02545 Prelamin-A/C Unclassified protein C00005372 C00005373 11 / 10
P06280 Alpha-galactosidase A Enzyme C00005372 C00005373 1 / 1
Q16637 Survival motor neuron protein Unclassified protein C00005372 C00005373 4 / 1
P10696 Alkaline phosphatase, placental-like Enzyme C00005372 C00005373 0 / 1
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00005372 C00005373 3 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00005372 C00005373 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002743 C00003672 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002743 C00003672 0 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00005372 C00005373 0 / 1
P22303 Acetylcholinesterase Hydrolase C00002743 C00005413 1 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00002743 C00005413 0 / 0
Q01196 Runt-related transcription factor 1 Unclassified protein C00005372 C00005373 1 / 4
P04062 Glucosylceramidase Enzyme C00005372 C00005373 6 / 4
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002743 C00003672 1 / 1
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00005372 C00005373 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00005372 C00005373 0 / 0
P34949 Mannose-6-phosphate isomerase Enzyme C00005372 C00005373 1 / 1
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00005372 C00005373 1 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002743 C00003672 1 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00002743 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00002743 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002743 1 / 8
P11388 DNA topoisomerase 2-alpha Isomerase C00005413 0 / 0
P14416 D(2) dopamine receptor Dopamine receptor C00002743 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002743 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00002743 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00002743 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00002743 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00002743 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00002743 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00002743 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00002743 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00002743 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00002743 1 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00002743 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00005374 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00002743 1 / 2
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00002743 0 / 0
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00002743 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00002743 0 / 0
P42858 Huntingtin Unclassified protein C00002682 1 / 1
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00002743 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00002743 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00002743 0 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00002743 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00002743 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00002743 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00002743 1 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00002743 1 / 0
Q92731 Estrogen receptor beta NR3A2 C00002743 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00002743 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00002743 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00002743 0 / 0
P25021 Histamine H2 receptor Histamine receptor C00002743 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00002743 1 / 0
P00915 Carbonic anhydrase 1 Lyase C00002743 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00002743 0 / 0
P08311 Cathepsin G S1A C00002743 0 / 0
P27487 Dipeptidyl peptidase 4 S9B C00005413 0 / 1
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00002743 1 / 0
P03956 Interstitial collagenase M10A C00002743 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00002743 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002743 1 / 1
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00002743 0 / 1
P00918 Carbonic anhydrase 2 Lyase C00002743 1 / 2
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00005374 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00005413 0 / 0
P00734 Prothrombin S1A C00003672 4 / 2
P04150 Glucocorticoid receptor NR3C1 C00002743 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00002743 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00002743 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00029633 2 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00002743 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00002743 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00002743 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00002743 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00002743 0 / 0
P06276 Cholinesterase Hydrolase C00005413 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00002743 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00002743 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00002743 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00002743 1 / 0
P14780 Matrix metalloproteinase-9 M10A C00002743 2 / 2
P27361 Mitogen-activated protein kinase 3 Erk C00002743 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00002743 2 / 1
P17252 Protein kinase C alpha type Alpha C00002743 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00002743 0 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00005413 3 / 3
P29466 Caspase-1 C14 C00002743 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00002743 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00002743 0 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00002743 1 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00002743 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00002743 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00002743 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00002743 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00002743 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00002743 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00002743 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00002743 0 / 0
P51580 Thiopurine S-methyltransferase Enzyme C00002682 1 / 1
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00002743 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00002743 0 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00002743 0 / 0
Q13093 Platelet-activating factor acetylhydrolase Enzyme C00002743 3 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00005374 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00002743 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00002743 5 / 1
P08246 Neutrophil elastase S1A C00002743 2 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00002743 2 / 2
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00002743 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00002743 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00002743 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00002743 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00002743 1 / 1
P07451 Carbonic anhydrase 3 Lyase C00002743 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00002743 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00002743 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00002743 0 / 0
P48147 Prolyl endopeptidase S9A C00005413 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00002743 1 / 1
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q12794 Hyaluronidase-1 Enzyme C00002743 1 / 2
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
Q9P1W9 Serine/threonine-protein kinase pim-2 Pim C00005374 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00029633 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 1 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00002743 3 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00005413 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00002743 0 / 0

45 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002743 C00005374 C00005413
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00002743 C00005413
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00005374 C00005413
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) C00002682 C00002743
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002682 C00002743
581 BAX, BCL2L4 BCL2-associated X protein C00005372 C00005413
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00002743 C00005413
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002682 C00002743
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002743 C00005413
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002682 C00002743
196 AHR, bHLHe76 aryl hydrocarbon receptor C00005413
7299 TYR, ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3 tyrosinase (EC:1.14.18.1) C00002743
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00002743
5742 PTGS1, COX1, COX3, PCOX1, PES-1, PGG/HS, PGHS-1, PGHS1, PHS1, PTGHS prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002743
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00002743
23621 BACE1, ASP2, BACE, HSPC104 beta-site APP-cleaving enzyme 1 (EC:3.4.23.46) C00002743
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00002743
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00002743
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00005372
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00005372
23411 SIRT1, SIR2L1 sirtuin 1 C00005372
177 AGER, RAGE advanced glycosylation end product-specific receptor C00005413
6319 SCD, FADS5, MSTP008, SCD1, SCDOS stearoyl-CoA desaturase (delta-9-desaturase) (EC:1.14.19.1) C00002743
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00005413
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00005413
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00005413
847 CAT catalase (EC:1.11.1.6) C00005413
873 CBR1, CBR, SDR21C1, hCBR1 carbonyl reductase 1 (EC:1.1.1.189 1.1.1.197 1.1.1.184) C00005413
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00005413
3627 CXCL10, C7, IFI10, INP10, IP-10, SCYB10, crg-2, gIP-10, mob-1 chemokine (C-X-C motif) ligand 10 C00005413
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00005413
2936 GSR glutathione reductase (EC:1.8.1.7) C00005413
3458 IFNG, IFG, IFI interferon, gamma C00005413
3480 IGF1R, CD221, IGFIR, IGFR, JTK13 insulin-like growth factor 1 receptor (EC:2.7.10.1) C00005413
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00005413
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00005413
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00005413
3667 IRS1, HIRS-1 insulin receptor substrate 1 C00005413
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00005413
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00005413
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00005413
7039 TGFA, TFGA transforming growth factor, alpha C00005413
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00005413
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00005413
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00002682

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (109)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#600807 Asthma, susceptibility to Q13093
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#614490 Blood group, junior system; jr Q9UNQ0
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#602579 Congenital disorder of glycosylation, type ib; cdg1b P34949
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 P04626
#232300 Glycogen storage disease ii P10253
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#147050 Ige responsiveness, atopic; iger Q13093
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#601626 Leukemia, acute myeloid; aml P36888
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#300705 Mental retardation, x-linked 17; mrx17 Q99714
%300852 Mental retardation, x-linked 88; mrx88 P50052
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#601492 Mucopolysaccharidosis, type ix; mps9 Q12794
#126200 Multiple sclerosis, susceptibility to; ms P08575
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#614674 Periodic fever, menstrual cycle-dependent P08908
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614278 Platelet-activating factor acetylhydrolase deficiency; pafad Q13093
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#610460 Thiopurine s-methyltransferase deficiency P51580
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#190300 Tremor, hereditary essential, 1; etm1 P35462
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (80)

KEGG name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00213 Hypophosphatasia P05186 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00023 Testicular cancer P10696 (marker)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H00032 Thyroid cancer P27487 (marker)
H01171 Poor drug metabolism (PM) P33261 (related)
H00118 Congenital disorders of glycosylation (CDG) type I P34949 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00059 Huntington's disease (HD) P42858 (related)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00133 Mucopolysaccharidosis type IX (MPS9) Q12794 (related)
H00421 Mucopolysaccharidosis (MPS) Q12794 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

15 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D050197 Atherosclerosis C00002743
D002252 Carbon Tetrachloride Poisoning C00002743
D007249 Inflammation C00002743
D008106 Liver Cirrhosis, Experimental C00002743
D008545 Melanoma C00002743
D009203 Myocardial Infarction C00002743
D010146 Pain C00005374
D001424 Bacterial Infections C00005413
D003092 Colitis C00005413
D004409 Dyskinesia, Drug-Induced C00005413
D015212 Inflammatory Bowel Diseases C00005413
D007674 Kidney Diseases C00005413
D028361 Mitochondrial Diseases C00005413
D010243 Paralysis C00005413
D013276 Stomach Ulcer C00005413