BDBM50407274 CHEMBL2111954

SMILES: CC(C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(O)CC(=O)N[C@@H](Cc1ccccc1)C(N)=O

InChI Key: InChIKey=SIWWBMPDKOPPFT-WQPIWFEDSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50407274   

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
Gastrin releasing peptide receptor (MOUSE)	BDBM50407274 (CHEMBL2111954) Show SMILES CC(C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(O)CC(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C59H74N14O10/c1-34(2)52(58(82)67-35(3)54(78)71-47(27-41-31-62-33-65-41)59(83)73-23-13-20-48(73)49(74)28-51(76)68-44(53(60)77)24-38-16-9-6-10-17-38)72-55(79)36(4)66-56(80)45(25-39-29-63-43-19-12-11-18-42(39)43)70-57(81)46(26-40-30-61-32-64-40)69-50(75)22-21-37-14-7-5-8-15-37/h5-12,14-19,29-36,44-49,52,63,74H,13,20-28H2,1-4H3,(H2,60,77)(H,61,64)(H,62,65)(H,66,80)(H,67,82)(H,68,76)(H,69,75)(H,70,81)(H,71,78)(H,72,79)/t35-,36-,44-,45-,46-,47-,48-,49?,52-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	31	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Company Curated by ChEMBL					Assay Description Ability of peptide to inhibit binding of 10 pM [125I]-gastrin releasing peptide to S-3T3 cell membrane.				J Med Chem 37: 439-45 (1994) BindingDB Entry DOI: 10.7270/Q2ST7NXN
					More data for this Ligand-Target Pair
Gastrin releasing peptide receptor (MOUSE)	BDBM50407274 (CHEMBL2111954) Show SMILES CC(C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(O)CC(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C59H74N14O10/c1-34(2)52(58(82)67-35(3)54(78)71-47(27-41-31-62-33-65-41)59(83)73-23-13-20-48(73)49(74)28-51(76)68-44(53(60)77)24-38-16-9-6-10-17-38)72-55(79)36(4)66-56(80)45(25-39-29-63-43-19-12-11-18-42(39)43)70-57(81)46(26-40-30-61-32-64-40)69-50(75)22-21-37-14-7-5-8-15-37/h5-12,14-19,29-36,44-49,52,63,74H,13,20-28H2,1-4H3,(H2,60,77)(H,61,64)(H,62,65)(H,66,80)(H,67,82)(H,68,76)(H,69,75)(H,70,81)(H,71,78)(H,72,79)/t35-,36-,44-,45-,46-,47-,48-,49?,52-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
Burroughs Wellcome Company Curated by ChEMBL					Assay Description The ability of the peptide to inhibit the binding of 50 pM [125I]-Gastrin releasing peptide to intact S-3T3 cells				J Med Chem 37: 439-45 (1994) BindingDB Entry DOI: 10.7270/Q2ST7NXN
					More data for this Ligand-Target Pair