Metabolite

KNApSAcK Entry

id C00001490
Name Adenine
CAS RN 73-24-5
Standard InChI InChI=1S/C5H5N5/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H3,6,7,8,9,10)
Standard InChI (Main Layer) InChI=1S/C5H5N5/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H3,6,7,8,9,10)

Cluster

Phytochemical cluster
KCF-S cluster No. 6151

Link

ChEMBL

By standard InChI CHEMBL226345
By standard InChI Main Layer CHEMBL226345

KEGG

By LinkDB C00147

CTD

By CAS RN D000225

Human Protein / Gene in interaction

52 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q02750 Dual specificity mitogen-activated protein kinase kinase 1 Ste7 CHEMBL226345 CHEMBL830657 (1)
1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase CHEMBL226345 CHEMBL1664429 (1)
0 / 0
P08069 Insulin-like growth factor 1 receptor TK tyrosine-protein kinase INSR subfamily CHEMBL226345 CHEMBL1819993 (1)
1 / 3
Q16539 Mitogen-activated protein kinase 14 p38 CHEMBL226345 CHEMBL830639 (1) CHEMBL1819997 (1)
0 / 0
P22894 Neutrophil collagenase M10A CHEMBL226345 CHEMBL1664434 (1)
0 / 0
P42336 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform Enzyme CHEMBL226345 CHEMBL1820089 (1)
9 / 1
P45984 Mitogen-activated protein kinase 9 Jnk CHEMBL226345 CHEMBL832006 (1)
0 / 0
P17252 Protein kinase C alpha type Alpha CHEMBL226345 CHEMBL831280 (1)
0 / 0
P27361 Mitogen-activated protein kinase 3 Erk CHEMBL226345 CHEMBL832021 (1)
0 / 0
P14780 Matrix metalloproteinase-9 M10A CHEMBL226345 CHEMBL1664435 (1)
2 / 2
Q15303 Receptor tyrosine-protein kinase erbB-4 TK tyrosine-protein kinase EGFR subfamily CHEMBL226345 CHEMBL1819990 (1)
0 / 0
O14965 Aurora kinase A Aur CHEMBL226345 CHEMBL1819984 (1)
0 / 0
P02545 Prelamin-A/C Unclassified protein CHEMBL226345 CHEMBL1614544 (1)
11 / 10
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase CHEMBL226345 CHEMBL905368 (1) CHEMBL905369 (1)
1 / 1
P11309 Serine/threonine-protein kinase pim-1 Pim CHEMBL226345 CHEMBL1820091 (1)
0 / 0
P06493 Cyclin-dependent kinase 1 Cdc2 CHEMBL226345 CHEMBL657992 (1)
0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily CHEMBL226345 CHEMBL1819987 (1)
1 / 11
P31751 RAC-beta serine/threonine-protein kinase Akt CHEMBL226345 CHEMBL1819982 (1)
2 / 2
O14920 Inhibitor of nuclear factor kappa-B kinase subunit beta Other serine/threonine protein kinase CHEMBL226345 CHEMBL1819977 (1)
0 / 0
Q13464 Rho-associated protein kinase 1 Rock CHEMBL226345 CHEMBL831996 (1) CHEMBL1820093 (1)
0 / 0
O43353 Receptor-interacting serine/threonine-protein kinase 2 Ripk CHEMBL226345 CHEMBL1820092 (1)
0 / 0
P07332 Tyrosine-protein kinase Fes/Fps Fer CHEMBL226345 CHEMBL1819988 (1)
0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk CHEMBL226345 CHEMBL831995 (1) CHEMBL1819992 (1)
0 / 0
Q05397 Focal adhesion kinase 1 Fak CHEMBL226345 CHEMBL1819991 (1)
0 / 0
P03956 Interstitial collagenase M10A CHEMBL226345 CHEMBL1664431 (1)
0 / 1
Q99683 Mitogen-activated protein kinase kinase kinase 5 Ste11 CHEMBL226345 CHEMBL1819983 (1)
0 / 0
P15056 Serine/threonine-protein kinase B-raf Raf CHEMBL226345 CHEMBL1819986 (1)
6 / 3
Q99816 Tumor susceptibility gene 101 protein Unclassified protein CHEMBL226345 CHEMBL1738574 (1)
0 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily CHEMBL226345 CHEMBL1819989 (1)
5 / 10
Q96GD4 Aurora kinase B Aur CHEMBL226345 CHEMBL1819985 (1)
0 / 0
P49137 MAP kinase-activated protein kinase 2 CAMK serine/threonine protein kinase MAPKAPK CHEMBL226345 CHEMBL1819996 (1)
0 / 0
P28482 Mitogen-activated protein kinase 1 Erk CHEMBL226345 CHEMBL832022 (1)
0 / 0
P45983 Mitogen-activated protein kinase 8 Jnk CHEMBL226345 CHEMBL832005 (1) CHEMBL1819979 (1)
0 / 0
P08253 72 kDa type IV collagenase M10A CHEMBL226345 CHEMBL1664432 (1)
1 / 3
Q13177 Serine/threonine-protein kinase PAK 2 STE serine/threonine protein kinase PAKA subfamily CHEMBL226345 CHEMBL1820087 (1)
0 / 0
Q08881 Tyrosine-protein kinase ITK/TSK Tec CHEMBL226345 CHEMBL1819994 (1)
1 / 1
O00329 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform Enzyme CHEMBL226345 CHEMBL1820090 (1)
0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein CHEMBL226345 CHEMBL1028564 (1)
0 / 0
P31749 RAC-alpha serine/threonine-protein kinase Akt CHEMBL226345 CHEMBL830592 (1) CHEMBL1819981 (1)
4 / 1
Q15118 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial Pdhk CHEMBL226345 CHEMBL1820088 (1)
0 / 0
O00141 Serine/threonine-protein kinase Sgk1 AGC serine/threonine protein kinase SGK subfamily CHEMBL226345 CHEMBL1820094 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL226345 CHEMBL1738184 (1)
0 / 0
P06239 Tyrosine-protein kinase Lck Src CHEMBL226345 CHEMBL832023 (1)
0 / 1
P52333 Tyrosine-protein kinase JAK3 Jakb CHEMBL226345 CHEMBL1819995 (1)
1 / 1
P04049 RAF proto-oncogene serine/threonine-protein kinase Raf CHEMBL226345 CHEMBL832054 (1)
2 / 0
P43405 Tyrosine-protein kinase SYK Syk CHEMBL226345 CHEMBL1820095 (1)
0 / 0
P08254 Stromelysin-1 M10A CHEMBL226345 CHEMBL1664433 (1)
1 / 0
P48736 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform Enzyme CHEMBL226345 CHEMBL1819978 (1)
0 / 0
P22694 cAMP-dependent protein kinase catalytic subunit beta Pka CHEMBL226345 CHEMBL831286 (1)
0 / 0
P17612 cAMP-dependent protein kinase catalytic subunit alpha Pka CHEMBL226345 CHEMBL831286 (1)
0 / 0
P22612 cAMP-dependent protein kinase catalytic subunit gamma Pka CHEMBL226345 CHEMBL831286 (1)
0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein CHEMBL226345 CHEMBL2354287 (1)
1 / 1

CTD interaction (1)

compound gene gene name gene description interaction interaction type form reference
pmid
D000225 3576 IL8
CXCL8
GCP-1
GCP1
LECT
LUCT
LYNAP
MDNCF
MONAP
NAF
NAP-1
NAP1
interleukin 8 Adenine inhibits the reaction [deoxynivalenol results in increased expression of IL8 protein] decreases reaction
/ increases expression
protein 18308354

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (44)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#114480 Breast cancer P31749
P42336
#115150 Cardiofaciocutaneous syndrome 1; cfc1 P15056
#615279 Cardiofaciocutaneous syndrome 3; cfc3 Q02750
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P15056
P31749
P42336
#612918 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi P42336
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#615108 Cowden syndrome 5; cws5 P42336
#615109 Cowden syndrome 6; cws6 P31749
#125853 Diabetes mellitus, noninsulin-dependent; niddm P31751
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#137800 Glioma susceptibility 1; glm1 P04626
#610140 Heart-hand syndrome, slovenian type P02545
#114550 Hepatocellular carcinoma P42336
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#240900 Hypoinsulinemic hypoglycemia with hemihypertrophy; hihghh P31751
#270450 Insulin-like growth factor i, resistance to P08069
#603932 Intervertebral disc disease; idd P14780
#182000 Keratosis, seborrheic P42336
#611554 Leopard syndrome 2 P04049
#613707 Leopard syndrome 3 P15056
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#211980 Lung cancer P00533
P04626
P15056
#605027 Lymphoma, non-hodgkin, familial P15056
#613011 Lymphoproliferative syndrome 1; lpfs1 Q08881
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#602501 Megalencephaly-capillary malformation-polymicrogyria syndrome; mcap P42336
#603387 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome; mpph P42336
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#611553 Noonan syndrome 5; ns5 P04049
#613706 Noonan syndrome 7; ns7 P15056
#167000 Ovarian cancer P04626
P42336
#176920 Proteus syndrome P31749
#275210 Restrictive dermopathy, lethal P02545
#600802 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative P52333
#278300 Xanthinuria, type i P47989

KEGG DISEASE (38)

KEGG disease name UniProt
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
P08253 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P31751 (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)
H00019 Pancreatic cancer P04626 (related)
H00026 Endometrial Cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
P31751 (related)
P42336 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00015 Malignant pleural mesothelioma P08069 (related)
H00050 Synovial sarcoma P08069 (related)
H01274 Growth delay due to insulin-like growth factor I resistance P08069 (related)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00032 Thyroid cancer P15056 (related)
H00038 Malignant melanoma P15056 (related)
H00523 Noonan syndrome and related disorders P15056 (related)
Q02750 (related)
H00539 PTEN hamartoma tumor syndrome (PHTS) P31749 (related)
H00192 Xanthinuria P47989 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P52333 (related)
H00107 Other well-defined immunodeficiency syndromes Q08881 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)

Diseases related to CTD interactions

6 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D000855 D000225 Anorexia marker/mechanism
946274
D002779 D000225 Cholestasis marker/mechanism
946274
D056486 D000225 Drug-Induced Liver Injury marker/mechanism
946274
D007565 D000225 Jaundice marker/mechanism
946274
D009325 D000225 Nausea marker/mechanism
946274
D051437 D000225 Renal Insufficiency marker/mechanism
11758903