General Information of Drug Off-Target (DOT) (ID: OTH85PI5)

DOT Name Mitogen-activated protein kinase 1 (MAPK1)
Synonyms MAP kinase 1; MAPK 1; EC 2.7.11.24; ERT1; Extracellular signal-regulated kinase 2; ERK-2; MAP kinase isoform p42; p42-MAPK; Mitogen-activated protein kinase 2; MAP kinase 2; MAPK 2
Gene Name MAPK1
Related Disease
Noonan syndrome 13 ( )
UniProt ID
MK01_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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PDB ID
1PME ; 1TVO ; 1WZY ; 2OJG ; 2OJI ; 2OJJ ; 2Y9Q ; 3D42 ; 3D44 ; 3I5Z ; 3I60 ; 3SA0 ; 3TEI ; 3W55 ; 4FMQ ; 4FUX ; 4FUY ; 4FV0 ; 4FV1 ; 4FV2 ; 4FV3 ; 4FV4 ; 4FV5 ; 4FV6 ; 4FV7 ; 4FV8 ; 4FV9 ; 4G6N ; 4G6O ; 4H3P ; 4H3Q ; 4IZ5 ; 4IZ7 ; 4IZA ; 4N0S ; 4NIF ; 4O6E ; 4QP1 ; 4QP2 ; 4QP3 ; 4QP4 ; 4QP6 ; 4QP7 ; 4QP8 ; 4QP9 ; 4QPA ; 4QTA ; 4QTE ; 4XJ0 ; 4ZXT ; 4ZZM ; 4ZZN ; 4ZZO ; 5AX3 ; 5BUE ; 5BUI ; 5BUJ ; 5BVD ; 5BVE ; 5BVF ; 5K4I ; 5LCJ ; 5LCK ; 5NGU ; 5NHF ; 5NHH ; 5NHJ ; 5NHL ; 5NHO ; 5NHP ; 5NHV ; 5V60 ; 5V61 ; 5V62 ; 5WP1 ; 6D5Y ; 6DMG ; 6G54 ; 6G8X ; 6G91 ; 6G92 ; 6G93 ; 6G97 ; 6G9A ; 6G9D ; 6G9H ; 6G9J ; 6G9K ; 6G9M ; 6G9N ; 6GDM ; 6GDQ ; 6GE0 ; 6GJB ; 6GJD ; 6NBS ; 6OPG ; 6OPH ; 6OPI ; 6Q7K ; 6Q7S ; 6Q7T ; 6QA1 ; 6QA3 ; 6QA4 ; 6QAG ; 6QAH ; 6QAL ; 6QAQ ; 6QAW ; 6RQ4 ; 6SLG ; 7AUV ; 7E73 ; 7E75 ; 7NQQ ; 7NQW ; 7NR3 ; 7NR5 ; 7NR8 ; 7NR9 ; 7OPM ; 7W5O ; 7X4U ; 7XC1 ; 8AO2 ; 8AO3 ; 8AO4 ; 8AO5 ; 8AO6 ; 8AO7 ; 8AO8 ; 8AO9 ; 8AOA ; 8AOB ; 8AOC ; 8AOD ; 8AOE ; 8AOF ; 8AOG ; 8AOH ; 8AOI ; 8AOJ
EC Number
2.7.11.24
Pfam ID
PF00069
Sequence
MAAAAAAGAGPEMVRGQVFDVGPRYTNLSYIGEGAYGMVCSAYDNVNKVRVAIKKISPFE
HQTYCQRTLREIKILLRFRHENIIGINDIIRAPTIEQMKDVYIVQDLMETDLYKLLKTQH
LSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLLNTTCDLKICDFGLARVADPDHDH
TGFLTEYVATRWYRAPEIMLNSKGYTKSIDIWSVGCILAEMLSNRPIFPGKHYLDQLNHI
LGILGSPSQEDLNCIINLKARNYLLSLPHKNKVPWNRLFPNADSKALDLLDKMLTFNPHK
RIEVEQALAHPYLEQYYDPSDEPIAEAPFKFDMELDDLPKEKLKELIFEETARFQPGYRS
Function
Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway. MAPK1/ERK2 and MAPK3/ERK1 are the 2 MAPKs which play an important role in the MAPK/ERK cascade. They participate also in a signaling cascade initiated by activated KIT and KITLG/SCF. Depending on the cellular context, the MAPK/ERK cascade mediates diverse biological functions such as cell growth, adhesion, survival and differentiation through the regulation of transcription, translation, cytoskeletal rearrangements. The MAPK/ERK cascade also plays a role in initiation and regulation of meiosis, mitosis, and postmitotic functions in differentiated cells by phosphorylating a number of transcription factors. About 160 substrates have already been discovered for ERKs. Many of these substrates are localized in the nucleus, and seem to participate in the regulation of transcription upon stimulation. However, other substrates are found in the cytosol as well as in other cellular organelles, and those are responsible for processes such as translation, mitosis and apoptosis. Moreover, the MAPK/ERK cascade is also involved in the regulation of the endosomal dynamics, including lysosome processing and endosome cycling through the perinuclear recycling compartment (PNRC); as well as in the fragmentation of the Golgi apparatus during mitosis. The substrates include transcription factors (such as ATF2, BCL6, ELK1, ERF, FOS, HSF4 or SPZ1), cytoskeletal elements (such as CANX, CTTN, GJA1, MAP2, MAPT, PXN, SORBS3 or STMN1), regulators of apoptosis (such as BAD, BTG2, CASP9, DAPK1, IER3, MCL1 or PPARG), regulators of translation (such as EIF4EBP1 and FXR1) and a variety of other signaling-related molecules (like ARHGEF2, DCC, FRS2 or GRB10). Protein kinases (such as RAF1, RPS6KA1/RSK1, RPS6KA3/RSK2, RPS6KA2/RSK3, RPS6KA6/RSK4, SYK, MKNK1/MNK1, MKNK2/MNK2, RPS6KA5/MSK1, RPS6KA4/MSK2, MAPKAPK3 or MAPKAPK5) and phosphatases (such as DUSP1, DUSP4, DUSP6 or DUSP16) are other substrates which enable the propagation the MAPK/ERK signal to additional cytosolic and nuclear targets, thereby extending the specificity of the cascade. Mediates phosphorylation of TPR in response to EGF stimulation. May play a role in the spindle assembly checkpoint. Phosphorylates PML and promotes its interaction with PIN1, leading to PML degradation. Phosphorylates CDK2AP2; Acts as a transcriptional repressor. Binds to a [GC]AAA[GC] consensus sequence. Repress the expression of interferon gamma-induced genes. Seems to bind to the promoter of CCL5, DMP1, IFIH1, IFITM1, IRF7, IRF9, LAMP3, OAS1, OAS2, OAS3 and STAT1. Transcriptional activity is independent of kinase activity.
KEGG Pathway
EGFR tyrosine ki.se inhibitor resistance (hsa01521 )
Endocrine resistance (hsa01522 )
Platinum drug resistance (hsa01524 )
MAPK sig.ling pathway (hsa04010 )
ErbB sig.ling pathway (hsa04012 )
Ras sig.ling pathway (hsa04014 )
Rap1 sig.ling pathway (hsa04015 )
cGMP-PKG sig.ling pathway (hsa04022 )
cAMP sig.ling pathway (hsa04024 )
Chemokine sig.ling pathway (hsa04062 )
HIF-1 sig.ling pathway (hsa04066 )
FoxO sig.ling pathway (hsa04068 )
Sphingolipid sig.ling pathway (hsa04071 )
Phospholipase D sig.ling pathway (hsa04072 )
Oocyte meiosis (hsa04114 )
Autophagy - animal (hsa04140 )
Efferocytosis (hsa04148 )
mTOR sig.ling pathway (hsa04150 )
PI3K-Akt sig.ling pathway (hsa04151 )
Apoptosis (hsa04210 )
Cellular senescence (hsa04218 )
Adrenergic sig.ling in cardiomyocytes (hsa04261 )
Vascular smooth muscle contraction (hsa04270 )
TGF-beta sig.ling pathway (hsa04350 )
Axon guidance (hsa04360 )
VEGF sig.ling pathway (hsa04370 )
Apelin sig.ling pathway (hsa04371 )
Osteoclast differentiation (hsa04380 )
Focal adhesion (hsa04510 )
Adherens junction (hsa04520 )
Gap junction (hsa04540 )
Sig.ling pathways regulating pluripotency of stem cells (hsa04550 )
Platelet activation (hsa04611 )
Neutrophil extracellular trap formation (hsa04613 )
Toll-like receptor sig.ling pathway (hsa04620 )
NOD-like receptor sig.ling pathway (hsa04621 )
C-type lectin receptor sig.ling pathway (hsa04625 )
.tural killer cell mediated cytotoxicity (hsa04650 )
IL-17 sig.ling pathway (hsa04657 )
Th1 and Th2 cell differentiation (hsa04658 )
Th17 cell differentiation (hsa04659 )
T cell receptor sig.ling pathway (hsa04660 )
B cell receptor sig.ling pathway (hsa04662 )
Fc epsilon RI sig.ling pathway (hsa04664 )
Fc gamma R-mediated phagocytosis (hsa04666 )
TNF sig.ling pathway (hsa04668 )
Circadian entrainment (hsa04713 )
Long-term potentiation (hsa04720 )
Neurotrophin sig.ling pathway (hsa04722 )
Retrograde endocan.binoid sig.ling (hsa04723 )
Glutamatergic sy.pse (hsa04724 )
Cholinergic sy.pse (hsa04725 )
Serotonergic sy.pse (hsa04726 )
Long-term depression (hsa04730 )
Regulation of actin cytoskeleton (hsa04810 )
Insulin sig.ling pathway (hsa04910 )
GnRH sig.ling pathway (hsa04912 )
Progesterone-mediated oocyte maturation (hsa04914 )
Estrogen sig.ling pathway (hsa04915 )
Melanogenesis (hsa04916 )
Prolactin sig.ling pathway (hsa04917 )
Thyroid hormone sig.ling pathway (hsa04919 )
Oxytocin sig.ling pathway (hsa04921 )
Relaxin sig.ling pathway (hsa04926 )
Parathyroid hormone synthesis, secretion and action (hsa04928 )
GnRH secretion (hsa04929 )
Type II diabetes mellitus (hsa04930 )
AGE-RAGE sig.ling pathway in diabetic complications (hsa04933 )
Cushing syndrome (hsa04934 )
Growth hormone synthesis, secretion and action (hsa04935 )
Aldosterone-regulated sodium reabsorption (hsa04960 )
Alzheimer disease (hsa05010 )
Prion disease (hsa05020 )
Pathways of neurodegeneration - multiple diseases (hsa05022 )
Alcoholism (hsa05034 )
Pathogenic Escherichia coli infection (hsa05130 )
Shigellosis (hsa05131 )
Salmonella infection (hsa05132 )
Pertussis (hsa05133 )
Yersinia infection (hsa05135 )
Leishmaniasis (hsa05140 )
Chagas disease (hsa05142 )
Toxoplasmosis (hsa05145 )
Tuberculosis (hsa05152 )
Hepatitis C (hsa05160 )
Hepatitis B (hsa05161 )
Human cytomegalovirus infection (hsa05163 )
Influenza A (hsa05164 )
Human papillomavirus infection (hsa05165 )
Human T-cell leukemia virus 1 infection (hsa05166 )
Kaposi sarcoma-associated herpesvirus infection (hsa05167 )
Human immunodeficiency virus 1 infection (hsa05170 )
Coro.virus disease - COVID-19 (hsa05171 )
Pathways in cancer (hsa05200 )
Viral carcinogenesis (hsa05203 )
Proteoglycans in cancer (hsa05205 )
MicroR.s in cancer (hsa05206 )
Chemical carcinogenesis - receptor activation (hsa05207 )
Chemical carcinogenesis - reactive oxygen species (hsa05208 )
Colorectal cancer (hsa05210 )
Re.l cell carcinoma (hsa05211 )
Pancreatic cancer (hsa05212 )
Endometrial cancer (hsa05213 )
Glioma (hsa05214 )
Prostate cancer (hsa05215 )
Thyroid cancer (hsa05216 )
Melanoma (hsa05218 )
Bladder cancer (hsa05219 )
Chronic myeloid leukemia (hsa05220 )
Acute myeloid leukemia (hsa05221 )
Non-small cell lung cancer (hsa05223 )
Breast cancer (hsa05224 )
Hepatocellular carcinoma (hsa05225 )
Gastric cancer (hsa05226 )
Central carbon metabolism in cancer (hsa05230 )
Choline metabolism in cancer (hsa05231 )
PD-L1 expression and PD-1 checkpoint pathway in cancer (hsa05235 )
Lipid and atherosclerosis (hsa05417 )
Reactome Pathway
RAF-independent MAPK1/3 activation (R-HSA-112409 )
MAPK1 (ERK2) activation (R-HSA-112411 )
Signaling by NODAL (R-HSA-1181150 )
Spry regulation of FGF signaling (R-HSA-1295596 )
Signaling by Activin (R-HSA-1502540 )
Golgi Cisternae Pericentriolar Stack Reorganization (R-HSA-162658 )
Frs2-mediated activation (R-HSA-170968 )
ERK/MAPK targets (R-HSA-198753 )
ERKs are inactivated (R-HSA-202670 )
Regulation of actin dynamics for phagocytic cup formation (R-HSA-2029482 )
Downregulation of SMAD2/3 (R-HSA-2173795 )
SMAD2/SMAD3 (R-HSA-2173796 )
Oxidative Stress Induced Senescence (R-HSA-2559580 )
Senescence-Associated Secretory Phenotype (SASP) (R-HSA-2559582 )
Oncogene Induced Senescence (R-HSA-2559585 )
FCERI mediated MAPK activation (R-HSA-2871796 )
Regulation of HSF1-mediated heat shock response (R-HSA-3371453 )
NCAM signaling for neurite out-growth (R-HSA-375165 )
Recycling pathway of L1 (R-HSA-437239 )
RSK activation (R-HSA-444257 )
Signal transduction by L1 (R-HSA-445144 )
Activation of the AP-1 family of transcription factors (R-HSA-450341 )
Thrombin signalling through proteinase activated receptors (PARs) (R-HSA-456926 )
Negative regulation of FGFR1 signaling (R-HSA-5654726 )
Negative regulation of FGFR2 signaling (R-HSA-5654727 )
Negative regulation of FGFR3 signaling (R-HSA-5654732 )
Negative regulation of FGFR4 signaling (R-HSA-5654733 )
RHO GTPases Activate WASPs and WAVEs (R-HSA-5663213 )
RHO GTPases Activate NADPH Oxidases (R-HSA-5668599 )
RAF/MAP kinase cascade (R-HSA-5673001 )
MAP2K and MAPK activation (R-HSA-5674135 )
Negative feedback regulation of MAPK pathway (R-HSA-5674499 )
Negative regulation of MAPK pathway (R-HSA-5675221 )
Neutrophil degranulation (R-HSA-6798695 )
Signaling by moderate kinase activity BRAF mutants (R-HSA-6802946 )
Signaling by high-kinase activity BRAF mutants (R-HSA-6802948 )
Signaling by BRAF and RAF1 fusions (R-HSA-6802952 )
Paradoxical activation of RAF signaling by kinase inactive BRAF (R-HSA-6802955 )
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling (R-HSA-6811558 )
Signal attenuation (R-HSA-74749 )
Interferon gamma signaling (R-HSA-877300 )
Advanced glycosylation endproduct receptor signaling (R-HSA-879415 )
Gastrin-CREB signalling pathway via PKC and MAPK (R-HSA-881907 )
ESR-mediated signaling (R-HSA-8939211 )
RUNX2 regulates osteoblast differentiation (R-HSA-8940973 )
Regulation of PTEN gene transcription (R-HSA-8943724 )
Regulation of the apoptosome activity (R-HSA-9627069 )
Estrogen-stimulated signaling through PRKCZ (R-HSA-9634635 )
Estrogen-dependent nuclear events downstream of ESR-membrane signaling (R-HSA-9634638 )
Suppression of apoptosis (R-HSA-9635465 )
Signaling downstream of RAS mutants (R-HSA-9649948 )
Signaling by MAP2K mutants (R-HSA-9652169 )
Signaling by MAPK mutants (R-HSA-9652817 )
Signaling by RAF1 mutants (R-HSA-9656223 )
FCGR3A-mediated phagocytosis (R-HSA-9664422 )
Nuclear events stimulated by ALK signaling in cancer (R-HSA-9725371 )
IFNG signaling activates MAPKs (R-HSA-9732724 )
NPAS4 regulates expression of target genes (R-HSA-9768919 )
Growth hormone receptor signaling (R-HSA-982772 )
phospho-PLA2 pathway (R-HSA-111995 )

Molecular Interaction Atlas (MIA) of This DOT

1 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Noonan syndrome 13 DISBYU1Y Strong Autosomal dominant [1]
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Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
This DOT Affected the Drug Response of 4 Drug(s)
Drug Name Drug ID Highest Status Interaction REF
Dacarbazine DMNPZL4 Approved Mitogen-activated protein kinase 1 (MAPK1) decreases the response to substance of Dacarbazine. [99]
Urokinase DM0GOUD Approved Mitogen-activated protein kinase 1 (MAPK1) increases the Diabetes mellitus ADR of Urokinase. [100]
PF-04691502 DMS610L Phase 2 Mitogen-activated protein kinase 1 (MAPK1) affects the response to substance of PF-04691502. [101]
3R14S-OCHRATOXIN A DM2KEW6 Investigative Mitogen-activated protein kinase 1 (MAPK1) increases the response to substance of 3R14S-OCHRATOXIN A. [102]
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69 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate increases the methylation of Mitogen-activated protein kinase 1 (MAPK1). [2]
Ciclosporin DMAZJFX Approved Ciclosporin increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [3]
Tretinoin DM49DUI Approved Tretinoin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [4]
Acetaminophen DMUIE76 Approved Acetaminophen increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [5]
Cisplatin DMRHGI9 Approved Cisplatin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [8]
Arsenic DMTL2Y1 Approved Arsenic increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [11]
Quercetin DM3NC4M Approved Quercetin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [12]
Temozolomide DMKECZD Approved Temozolomide increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [13]
Decitabine DMQL8XJ Approved Decitabine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [21]
Zoledronate DMIXC7G Approved Zoledronate decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [23]
Phenobarbital DMXZOCG Approved Phenobarbital increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [24]
Progesterone DMUY35B Approved Progesterone decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [25]
Menadione DMSJDTY Approved Menadione increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [26]
Fluorouracil DMUM7HZ Approved Fluorouracil increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [27]
Fulvestrant DM0YZC6 Approved Fulvestrant increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [28]
Folic acid DMEMBJC Approved Folic acid increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [30]
Niclosamide DMJAGXQ Approved Niclosamide decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [31]
Troglitazone DM3VFPD Approved Troglitazone decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [34]
Hydroquinone DM6AVR4 Approved Hydroquinone decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [35]
Rosiglitazone DMILWZR Approved Rosiglitazone increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [36]
Azathioprine DMMZSXQ Approved Azathioprine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [37]
Ethanol DMDRQZU Approved Ethanol decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [38]
Etoposide DMNH3PG Approved Etoposide increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [40]
Diclofenac DMPIHLS Approved Diclofenac increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [42]
Sodium lauryl sulfate DMLJ634 Approved Sodium lauryl sulfate increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [44]
Dasatinib DMJV2EK Approved Dasatinib decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [45]
Indomethacin DMSC4A7 Approved Indomethacin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [46]
Mitomycin DMH0ZJE Approved Mitomycin increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [47]
Permethrin DMZ0Q1G Approved Permethrin decreases the methylation of Mitogen-activated protein kinase 1 (MAPK1). [48]
Gemcitabine DMSE3I7 Approved Gemcitabine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [51]
Sulindac DM2QHZU Approved Sulindac increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [52]
Methamphetamine DMPM4SK Approved Methamphetamine affects the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [54]
Daunorubicin DMQUSBT Approved Daunorubicin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [55]
Pioglitazone DMKJ485 Approved Pioglitazone decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [56]
Acocantherin DM7JT24 Approved Acocantherin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [57]
Thalidomide DM70BU5 Approved Thalidomide increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [58]
Phenytoin DMNOKBV Approved Phenytoin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [60]
Ursodeoxycholic acid DMCUT21 Approved Ursodeoxycholic acid increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [62]
Fluoxetine DM3PD2C Approved Fluoxetine decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [65]
Sodium phenylbutyrate DMXLBCQ Approved Sodium phenylbutyrate decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [66]
Beta-carotene DM0RXBT Approved Beta-carotene increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [67]
Imatinib DM7RJXL Approved Imatinib decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [68]
Sertraline DM0FB1J Approved Sertraline increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [69]
Estrone DM5T6US Approved Estrone increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [70]
Docetaxel DMDI269 Approved Docetaxel increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [72]
Isoproterenol DMK7MEY Approved Isoproterenol increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [73]
Propofol DMB4OLE Approved Propofol decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [76]
Glucosamine DM4ZLFD Approved Glucosamine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [77]
Isoniazid DM5JVS3 Approved Isoniazid decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [78]
Sevoflurane DMC9O43 Approved Sevoflurane increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [76]
Adenosine DMM2NSK Approved Adenosine decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [79]
Morphine DMRMS0L Approved Morphine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [80]
Eicosapentaenoic acid/docosa-hexaenoic acid DMMUCG4 Approved Eicosapentaenoic acid/docosa-hexaenoic acid increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [81]
Dihydroxyacetone DMM1LG2 Approved Dihydroxyacetone increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [82]
Crizotinib DM4F29C Approved Crizotinib decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [83]
Ciprofloxacin XR DM2NLS9 Approved Ciprofloxacin XR increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [84]
Cantharidin DMBP5N3 Approved Cantharidin increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [85]
Tetracycline DMZA017 Approved Tetracycline decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [86]
Methimazole DM25FL8 Approved Methimazole decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [87]
Mebendazole DMO14SG Approved Mebendazole increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [88]
Romidepsin DMT5GNL Approved Romidepsin decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [89]
Trovafloxacin DM6AN32 Approved Trovafloxacin increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [91]
Ergotidine DM78IME Approved Ergotidine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [92]
Masoprocol DMMVNZ0 Approved Masoprocol decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [94]
Carvedilol DMHTEAO Approved Carvedilol increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [73]
Allopurinol DMLPAOB Approved Allopurinol increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [95]
Epirubicin DMPDW6T Approved Epirubicin increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [96]
Sanguinarine DMDINFS Approved Sanguinarine increases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [97]
Omacetaxine mepesuccinate DMPU2WX Approved Omacetaxine mepesuccinate decreases the phosphorylation of Mitogen-activated protein kinase 1 (MAPK1). [98]
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⏷ Show the Full List of 69 Drug(s)
31 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [6]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate increases the expression of Mitogen-activated protein kinase 1 (MAPK1). [7]
Estradiol DMUNTE3 Approved Estradiol decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [9]
Ivermectin DMDBX5F Approved Ivermectin decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [10]
Arsenic trioxide DM61TA4 Approved Arsenic trioxide increases the expression of Mitogen-activated protein kinase 1 (MAPK1). [14]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [15]
Calcitriol DM8ZVJ7 Approved Calcitriol increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [16]
Vorinostat DMWMPD4 Approved Vorinostat decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [17]
Testosterone DM7HUNW Approved Testosterone increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [18]
Carbamazepine DMZOLBI Approved Carbamazepine affects the expression of Mitogen-activated protein kinase 1 (MAPK1). [19]
Methotrexate DM2TEOL Approved Methotrexate increases the expression of Mitogen-activated protein kinase 1 (MAPK1). [20]
Marinol DM70IK5 Approved Marinol increases the expression of Mitogen-activated protein kinase 1 (MAPK1). [22]
Dexamethasone DMMWZET Approved Dexamethasone decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [29]
Cannabidiol DM0659E Approved Cannabidiol decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [32]
Bortezomib DMNO38U Approved Bortezomib decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [33]
Aspirin DM672AH Approved Aspirin decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [39]
Paclitaxel DMLB81S Approved Paclitaxel decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [41]
Nicotine DMWX5CO Approved Nicotine increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [43]
Ethinyl estradiol DMODJ40 Approved Ethinyl estradiol increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [49]
Simvastatin DM30SGU Approved Simvastatin decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [50]
Capsaicin DMGMF6V Approved Capsaicin decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [53]
Lindane DMB8CNL Approved Lindane decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [59]
Sorafenib DMS8IFC Approved Sorafenib decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [61]
Gefitinib DM15F0X Approved Gefitinib decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [63]
Diphenylpyraline DMW4X37 Approved Diphenylpyraline decreases the expression of Mitogen-activated protein kinase 1 (MAPK1). [64]
Dinoprostone DMTYOPD Approved Dinoprostone increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [71]
Lovastatin DM9OZWQ Approved Lovastatin decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [50]
Ardeparin DMYRX8B Approved Ardeparin increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [74]
Adenosine triphosphate DM79F6G Approved Adenosine triphosphate increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [75]
Lapatinib DM3BH1Y Approved Lapatinib decreases the activity of Mitogen-activated protein kinase 1 (MAPK1). [90]
Busulfan DMXYJ9C Approved Busulfan increases the activity of Mitogen-activated protein kinase 1 (MAPK1). [93]
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⏷ Show the Full List of 31 Drug(s)

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98 Homoharringtonine suppresses LoVo cell growth by inhibiting EphB4 and the PI3K/AKT and MAPK/EKR1/2 signaling pathways. Food Chem Toxicol. 2020 Feb;136:110960. doi: 10.1016/j.fct.2019.110960. Epub 2019 Nov 11.
99 Exposure of melanoma cells to dacarbazine results in enhanced tumor growth and metastasis in vivo. J Clin Oncol. 2004 Jun 1;22(11):2092-100. doi: 10.1200/JCO.2004.11.070. Epub 2004 May 3.
100 ADReCS-Target: target profiles for aiding drug safety research and application. Nucleic Acids Res. 2018 Jan 4;46(D1):D911-D917. doi: 10.1093/nar/gkx899.
101 Synergistic inhibition of ovarian cancer cell growth by combining selective PI3K/mTOR and RAS/ERK pathway inhibitors. Eur J Cancer. 2013 Dec;49(18):3936-44. doi: 10.1016/j.ejca.2013.08.007. Epub 2013 Sep 3.
102 ERK and p38 MAPK signaling pathways are involved in ochratoxin A-induced G2 phase arrest in human gastric epithelium cells. Toxicol Lett. 2012 Mar 7;209(2):186-92. doi: 10.1016/j.toxlet.2011.12.011. Epub 2011 Dec 30.