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Drug ReportsAVUTOMETINIB
Avutometinib
Avutometinib is a small molecule pharmaceutical. It is currently being investigated in clinical studies. It is known to target dual specificity mitogen-activated protein kinase kinase 1 and RAF proto-oncogene serine/threonine-protein kinase.
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Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
26 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Ovarian neoplasmsD010051EFO_0003893C56141——6
Ovarian epithelial carcinomaD000077216———41——5
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Lung neoplasmsD008175HP_0100526C34.9044———6
Non-small-cell lung carcinomaD002289——43———5
NeoplasmsD009369—C8043———5
Brain neoplasmsD001932EFO_0003833C7132———3
Pancreatic neoplasmsD010190EFO_0003860C2521———2
Endometrioid carcinomaD018269——11———2
MelanomaD008545——12———2
Colorectal neoplasmsD015179——12———2
AdenocarcinomaD000230——12———2
Neoplasm metastasisD009362EFO_0009708—22———2
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple myelomaD009101—C90.01————1
Plasma cell neoplasmsD054219——1————1
NeuroblastomaD009447EFO_0000621—1————1
Central nervous system neoplasmsD016543——1————1
Plexiform neurofibromaD018318EFO_0000658—1————1
Nervous system neoplasmsD009423——1————1
Optic nerve gliomaD020339——1————1
NeurofibromatosesD017253—Q85.001————1
NeurofibromaD009455EFO_0000622—1————1
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameAvutometinib
INNavutometinib
Description
CH5126766 is a member of the class of coumarins that is 4-methyl-7-[(pyrimidin-2-yl)oxy]coumarin carrying an additional [2-[(methylaminosulfonyl)amino]-3-fluoropyridin-4-yl]methyl substituent at position 3. It has a role as an EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor and an antineoplastic agent. It is an aryloxypyrimidine, a member of coumarins, a member of pyridines, an organofluorine compound and a member of sulfamides.
Classification
Small molecule
Drug classtyrosine kinase inhibitors: tyrosine kinase inhibitors; MEK (MAPK kinase) inhibitors
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Structure (InChI/SMILES or Protein Sequence)
CNS(=O)(=O)Nc1nccc(Cc2c(C)c3ccc(Oc4ncccn4)cc3oc2=O)c1F
Identifiers
PDB—
CAS-ID946128-88-7
RxCUI—
ChEMBL IDCHEMBL3264002
ChEBI ID78825
PubChem CID16719221
DrugBankDB15254
UNII IDD0D4252V97 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
MAP2K1
MAP2K1
RAF1
RAF1
Organism
Homo sapiens
Gene name
MAP2K1
Gene synonyms
MEK1, PRKMK1
NCBI Gene ID
Protein name
dual specificity mitogen-activated protein kinase kinase 1
Protein synonyms
ERK activator kinase 1, MAPK/ERK kinase 1, MAPKK 1, MEK 1, protein kinase, mitogen-activated, kinase 1 (MAP kinase kinase 1)
Uniprot ID
Mouse ortholog
Map2k1 (26395)
dual specificity mitogen-activated protein kinase kinase 1 (P31938)
Variants
No data
Financial
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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7 adverse events reported
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