BDBM50322368 (S)-5-((S)-1-((S)-2-((S)-1-((S)-1-((S)-1-carboxy-3-methylbutylamino)-3,3-dimethyl-1-oxobutan-2-ylamino)-3-(4-hydroxyphenyl)-1-oxopropan-2-ylcarbamoyl)pyrrolidin-1-yl)-5-guanidino-1-oxopentan-2-ylamino)-N,N,N,4-tetramethyl-5-oxopentan-1-aminium::CHEMBL1172376
SMILES CC(C)C[C@H](NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](C)CCC[N+](C)(C)C)C(C)(C)C)C(O)=O
InChI Key InChIKey=NWPZHWJQSGWXSJ-BJAKLJBYSA-O
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50322368
TargetNeurotensin receptor type 2(Homo sapiens (Human))
Medical University Of South Carolina Campus
Curated by ChEMBL
Medical University Of South Carolina Campus
Curated by ChEMBL
Affinity DataEC50: 54nMAssay Description:Binding affinity to human NTR2 by gamma countingMore data for this Ligand-Target Pair
TargetNeurotensin receptor type 2(Rattus norvegicus)
Medical University Of South Carolina Campus
Curated by ChEMBL
Medical University Of South Carolina Campus
Curated by ChEMBL
Affinity DataKd: 23nMAssay Description:Displacement of [125I]NT from rat NTR2 by gamma countingMore data for this Ligand-Target Pair
TargetNeurotensin receptor type 1(Homo sapiens (Human))
Medical University Of South Carolina Campus
Curated by ChEMBL
Medical University Of South Carolina Campus
Curated by ChEMBL
Affinity DataEC50: 11nMAssay Description:Binding affinity to human NTR1 by gamma countingMore data for this Ligand-Target Pair
TargetNeurotensin receptor type 1(Rattus norvegicus)
Medical University Of South Carolina Campus
Curated by ChEMBL
Medical University Of South Carolina Campus
Curated by ChEMBL
Affinity DataEC50: 28nMAssay Description:Agonist activity at rat NTR1 expressed in LTK cells assessed as calcium mobilizationMore data for this Ligand-Target Pair