Target
Mitogen-activated protein kinase 1
Ligand
BDBM418281
Substrate
n/a
Meas. Tech.
ChEMBL_2121006 (CHEMBL4830153)
IC50
12±n/a nM
Citation
 Heightman, TDBerdini, VBevan, LBuck, IMCarr, MGCourtin, ACoyle, JEDay, JEHEast, CFazal, LGriffiths-Jones, CMHoward, SKucia-Tran, JMartins, VMuench, SMunck, JMNorton, DO'Reilly, MPalmer, NPathuri, PPeakman, TMReader, MRees, DCRich, SJShah, AWallis, NGWalton, HWilsher, NEWoolford, AJCooke, MCousin, DOnions, SShannon, JWatts, JMurray, CW Discovery of ASTX029, A Clinical Candidate Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2. J Med Chem 64:12286-12303 (2021) [PubMed]  Article 
Target
Name:
Mitogen-activated protein kinase 1
Synonyms:
ERT1 | Extracellular signal-regulated kinase 2 | Extracellular signal-regulated kinase 2 (ERK-2) | Extracellular signal-regulated kinase 2 (ERK2) | MAP Kinase 2/ERK2 | MAPK 2 | Mitogen activated kinase 1 (ERK-2) | Mitogen-activated protein kinase 1 (ERK-2) | Mitogen-activated protein kinase 1 (ERK2) | Mitogen-activated protein kinase 2 | p42-MAPK | MK01_HUMAN | MAPK1 | ERK2 | PRKM1 | PRKM2
Type:
Ser/Thr Protein Kinase
Mol. Mass.:
41392.76
Organism:
Human
Description:
P28482
Residue:
360
Sequence:
MAAAAAAGAGPEMVRGQVFDVGPRYTNLSYIGEGAYGMVCSAYDNVNKVRVAIKKISPFEHQTYCQRTLREIKILLRFRHENIIGINDIIRAPTIEQMKDVYIVQDLMETDLYKLLKTQHLSNDHICYFLYQILRGLKYIHSANVLHRDLKPSNLLLNTTCDLKICDFGLARVADPDHDHTGFLTEYVATRWYRAPEIMLNSKGYTKSIDIWSVGCILAEMLSNRPIFPGKHYLDQLNHILGILGSPSQEDLNCIINLKARNYLLSLPHKNKVPWNRLFPNADSKALDLLDKMLTFNPHKRIEVEQALAHPYLEQYYDPSDEPIAEAPFKFDMELDDLPKEKLKELIFEETARFQPGYRS
  
Inhibitor
Name:
BDBM418281
Synonyms:
US10457669, Example 1072 | (2R)-2-[6-(5-chloro-2-{[(2S)-1- hydroxypropan-2-yl]amino}pyrimidin- 4-yl)-1-oxo-2,3-dihydro-1H-isoindol-2- yl]N-[(1S)-1-(3-fluoro-5- methoxyphenyl)-2- hydroxyethyl]propanamide | US11001575, Example 1072
Type:
Small organic molecule
Emp. Form.:
TBD
Mol. Mass.:
TBD
SMILES:
TBD
Structure:
Search PDB for entries with ligand similarity: