BDBM50114086 CHEMBL433413::MK-11::N-[1-(1-{1-[1-(5-Amino-1-carbamoyl-pentylcarbamoyl)-2-(1H-indol-3-yl)-ethylcarbamoyl]-4-guanidino-butylcarbamoyl}-2-phenyl-ethylcarbamoyl)-2-(3H-imidazol-4-yl)-ethyl]-succinamic acid

SMILES: NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O

InChI Key: InChIKey=XHTPNLWJKHXMSN-UBLLTGQXSA-N

Data: 3 KI  3 EC50

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 6 hits for monomerid = 50114086   

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
Melanocortin receptor 3 (Homo sapiens (Human))	BDBM50114086 (CHEMBL433413 | MK-11 | N-[1-(1-{1-[1-(5-Amino-1-ca...) Show SMILES NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O Show InChI InChI=1S/C42H57N13O8/c43-17-7-6-13-30(37(44)59)52-40(62)33(20-26-22-49-29-12-5-4-11-28(26)29)55-38(60)31(14-8-18-48-42(45)46)53-39(61)32(19-25-9-2-1-3-10-25)54-41(63)34(21-27-23-47-24-50-27)51-35(56)15-16-36(57)58/h1-5,9-12,22-24,30-34,49H,6-8,13-21,43H2,(H2,44,59)(H,47,50)(H,51,56)(H,52,62)(H,53,61)(H,54,63)(H,55,60)(H,57,58)(H4,45,46,48)/t30-,31-,32+,33-,34-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	140	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Binding affinity for human Melanocortin-3 receptor (hMC3R) expressed in HEK293 cells				J Med Chem 45: 2644-50 (2002) BindingDB Entry DOI: 10.7270/Q2RB75B3
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50114086 (CHEMBL433413 | MK-11 | N-[1-(1-{1-[1-(5-Amino-1-ca...) Show SMILES NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O Show InChI InChI=1S/C42H57N13O8/c43-17-7-6-13-30(37(44)59)52-40(62)33(20-26-22-49-29-12-5-4-11-28(26)29)55-38(60)31(14-8-18-48-42(45)46)53-39(61)32(19-25-9-2-1-3-10-25)54-41(63)34(21-27-23-47-24-50-27)51-35(56)15-16-36(57)58/h1-5,9-12,22-24,30-34,49H,6-8,13-21,43H2,(H2,44,59)(H,47,50)(H,51,56)(H,52,62)(H,53,61)(H,54,63)(H,55,60)(H,57,58)(H4,45,46,48)/t30-,31-,32+,33-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	630	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Binding affinity for human Melanocortin-4 receptor (hMC4R)				J Med Chem 45: 2644-50 (2002) BindingDB Entry DOI: 10.7270/Q2RB75B3
					More data for this Ligand-Target Pair
Melanocortin receptor 5 (MC5R) (Homo sapiens (Human))	BDBM50114086 (CHEMBL433413 | MK-11 | N-[1-(1-{1-[1-(5-Amino-1-ca...) Show SMILES NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O Show InChI InChI=1S/C42H57N13O8/c43-17-7-6-13-30(37(44)59)52-40(62)33(20-26-22-49-29-12-5-4-11-28(26)29)55-38(60)31(14-8-18-48-42(45)46)53-39(61)32(19-25-9-2-1-3-10-25)54-41(63)34(21-27-23-47-24-50-27)51-35(56)15-16-36(57)58/h1-5,9-12,22-24,30-34,49H,6-8,13-21,43H2,(H2,44,59)(H,47,50)(H,51,56)(H,52,62)(H,53,61)(H,54,63)(H,55,60)(H,57,58)(H4,45,46,48)/t30-,31-,32+,33-,34-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	880	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Binding affinity for human melanocortin 5 receptor (hMC5R) expressed in HEK293 cells				J Med Chem 45: 2644-50 (2002) BindingDB Entry DOI: 10.7270/Q2RB75B3
					More data for this Ligand-Target Pair
Melanocortin receptor 3 (Homo sapiens (Human))	BDBM50114086 (CHEMBL433413 | MK-11 | N-[1-(1-{1-[1-(5-Amino-1-ca...) Show SMILES NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O Show InChI InChI=1S/C42H57N13O8/c43-17-7-6-13-30(37(44)59)52-40(62)33(20-26-22-49-29-12-5-4-11-28(26)29)55-38(60)31(14-8-18-48-42(45)46)53-39(61)32(19-25-9-2-1-3-10-25)54-41(63)34(21-27-23-47-24-50-27)51-35(56)15-16-36(57)58/h1-5,9-12,22-24,30-34,49H,6-8,13-21,43H2,(H2,44,59)(H,47,50)(H,51,56)(H,52,62)(H,53,61)(H,54,63)(H,55,60)(H,57,58)(H4,45,46,48)/t30-,31-,32+,33-,34-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	68	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Inhibition of human Melanocortin-3 receptor (hMC3R) expressed in HEK293 cells				J Med Chem 45: 2644-50 (2002) BindingDB Entry DOI: 10.7270/Q2RB75B3
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50114086 (CHEMBL433413 | MK-11 | N-[1-(1-{1-[1-(5-Amino-1-ca...) Show SMILES NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O Show InChI InChI=1S/C42H57N13O8/c43-17-7-6-13-30(37(44)59)52-40(62)33(20-26-22-49-29-12-5-4-11-28(26)29)55-38(60)31(14-8-18-48-42(45)46)53-39(61)32(19-25-9-2-1-3-10-25)54-41(63)34(21-27-23-47-24-50-27)51-35(56)15-16-36(57)58/h1-5,9-12,22-24,30-34,49H,6-8,13-21,43H2,(H2,44,59)(H,47,50)(H,51,56)(H,52,62)(H,53,61)(H,54,63)(H,55,60)(H,57,58)(H4,45,46,48)/t30-,31-,32+,33-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Inhibition of binding to human Melanocortin-4 receptor (hMC4R)				J Med Chem 45: 2644-50 (2002) BindingDB Entry DOI: 10.7270/Q2RB75B3
					More data for this Ligand-Target Pair
Melanocortin receptor 5 (MC5R) (Homo sapiens (Human))	BDBM50114086 (CHEMBL433413 | MK-11 | N-[1-(1-{1-[1-(5-Amino-1-ca...) Show SMILES NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCC(O)=O)C(N)=O Show InChI InChI=1S/C42H57N13O8/c43-17-7-6-13-30(37(44)59)52-40(62)33(20-26-22-49-29-12-5-4-11-28(26)29)55-38(60)31(14-8-18-48-42(45)46)53-39(61)32(19-25-9-2-1-3-10-25)54-41(63)34(21-27-23-47-24-50-27)51-35(56)15-16-36(57)58/h1-5,9-12,22-24,30-34,49H,6-8,13-21,43H2,(H2,44,59)(H,47,50)(H,51,56)(H,52,62)(H,53,61)(H,54,63)(H,55,60)(H,57,58)(H4,45,46,48)/t30-,31-,32+,33-,34-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Effective concentration against human melanocortin 5 receptor (hMC5R) in HEK293 cells				J Med Chem 45: 2644-50 (2002) BindingDB Entry DOI: 10.7270/Q2RB75B3
					More data for this Ligand-Target Pair