BDBM50040321 CHEMBL385805::PhCH2CH2(CO)His-Trp-Ala-Val-DAla-His-Sta-Phe-NH2

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

InChI Key: InChIKey=CAUWDHKNTABOGL-XMLFWXBDSA-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 = 50040321   

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)	BDBM50040321 (CHEMBL385805 | PhCH2CH2(CO)His-Trp-Ala-Val-DAla-Hi...) Show SMILES CC(C)CC(NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](C)NC(=O)[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(C)C)C(O)CC(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C60H78N14O10/c1-34(2)23-45(50(75)28-52(77)69-46(54(61)78)24-39-17-11-8-12-18-39)71-59(83)49(27-42-31-63-33-66-42)72-55(79)36(5)68-60(84)53(35(3)4)74-56(80)37(6)67-57(81)47(25-40-29-64-44-20-14-13-19-43(40)44)73-58(82)48(26-41-30-62-32-65-41)70-51(76)22-21-38-15-9-7-10-16-38/h7-20,29-37,45-50,53,64,75H,21-28H2,1-6H3,(H2,61,78)(H,62,65)(H,63,66)(H,67,81)(H,68,84)(H,69,77)(H,70,76)(H,71,83)(H,72,79)(H,73,82)(H,74,80)/t36-,37-,45?,46-,47-,48-,49-,50?,53-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.30	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)	BDBM50040321 (CHEMBL385805 | PhCH2CH2(CO)His-Trp-Ala-Val-DAla-Hi...) Show SMILES CC(C)CC(NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](C)NC(=O)[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(C)C)C(O)CC(=O)N[C@@H](Cc1ccccc1)C(N)=O Show InChI InChI=1S/C60H78N14O10/c1-34(2)23-45(50(75)28-52(77)69-46(54(61)78)24-39-17-11-8-12-18-39)71-59(83)49(27-42-31-63-33-66-42)72-55(79)36(5)68-60(84)53(35(3)4)74-56(80)37(6)67-57(81)47(25-40-29-64-44-20-14-13-19-43(40)44)73-58(82)48(26-41-30-62-32-65-41)70-51(76)22-21-38-15-9-7-10-16-38/h7-20,29-37,45-50,53,64,75H,21-28H2,1-6H3,(H2,61,78)(H,62,65)(H,63,66)(H,67,81)(H,68,84)(H,69,77)(H,70,76)(H,71,83)(H,72,79)(H,73,82)(H,74,80)/t36-,37-,45?,46-,47-,48-,49-,50?,53-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.30	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