BDBM50322391 (R)-1-(5-chloro-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amine::CHEMBL1173272
SMILES: N[C@@H]1CCN(C1)c1ncnc2[nH]cc(Cl)c12
InChI Key: InChIKey=KJNBPCKVXWYSHP-ZCFIWIBFSA-N
Data: 1 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
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RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50322391 ((R)-1-(5-chloro-7H-pyrrolo[2,3-d]pyrimidin-4-yl)py...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 68 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Global Research and Development Curated by ChEMBL | Assay Description Inhibition of AKT1 after 90 mins by IMAP assay | J Med Chem 53: 4615-22 (2010) Article DOI: 10.1021/jm1003842 BindingDB Entry DOI: 10.7270/Q24X580C | |||||||||||
More data for this Ligand-Target Pair |