BDBM50654013 CHEMBL6134691

SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CN(C)C(=O)CCOCCOCCNC(=O)CCCCCN1/C(=C\C=C\C2=[N+](C)c3ccccc3C2(C)C)C(C)(C)c2ccccc21)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)O

InChI Key

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50654013   

TargetType-2 angiotensin II receptor(Human)
Universite de Lorraine

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50654013BDBM50654013(CHEMBL6134691)
Affinity DataKi:  23nMAssay Description:Inhibition of PI3Kgamma assessed as inhibition of C5a-induced AKT phosphorylation at Ser473 by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/3/2026
Entry Details PubMed
TargetType-1 angiotensin II receptor(Human)
Universite de Lorraine

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50654013BDBM50654013(CHEMBL6134691)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of mTOR-mediated ribosomal protein S6 kinase phosphorylation by cell based assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/3/2026
Entry Details PubMed