Compile Data Set for Download or QSAR

Found 53 hits with Last Name = 'osada' and Initial = 's'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051610 (CHEMBL3311300) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC1=CCCCC1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r,t:10| Show InChI InChI=1S/C51H67N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h9-10,13-17,19-26,32-33,39-43H,8,11-12,18,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of fMLP-induced calcium mobilization incubated for 5 mins p...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
Histone deacetylase (Homo sapiens (Human))	BDBM50481610 (CHEMBL609609) Show SMILES F\C(CS)=C/CCCCCNC(=O)c1ccccc1 Show InChI InChI=1S/C15H20FNOS/c16-14(12-19)10-6-1-2-7-11-17-15(18)13-8-4-3-5-9-13/h3-5,8-10,19H,1-2,6-7,11-12H2,(H,17,18)/b14-10-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Inhibition of HDAC in human HeLa cell nuclear extract by fluorescence assay				Bioorg Med Chem 18: 605-11 (2010) Article DOI: 10.1016/j.bmc.2009.12.005 BindingDB Entry DOI: 10.7270/Q20C4ZMK
					More data for this Ligand-Target Pair
Histone deacetylase (Homo sapiens (Human))	BDBM50481612 (CHEMBL596660) Show SMILES CN(C)c1ccc(NC(=O)CCCCC\C=C(/F)CS)cc1 Show InChI InChI=1S/C17H25FN2OS/c1-20(2)16-11-9-15(10-12-16)19-17(21)8-6-4-3-5-7-14(18)13-22/h7,9-12,22H,3-6,8,13H2,1-2H3,(H,19,21)/b14-7-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Inhibition of HDAC in human HeLa cell nuclear extract by fluorescence assay				Bioorg Med Chem 18: 605-11 (2010) Article DOI: 10.1016/j.bmc.2009.12.005 BindingDB Entry DOI: 10.7270/Q20C4ZMK
					More data for this Ligand-Target Pair
Histone deacetylase (Homo sapiens (Human))	BDBM50481613 (CHEMBL597443) Show SMILES F\C(CS)=C/CCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C15H20FNOS/c16-13(12-19)8-4-1-2-7-11-15(18)17-14-9-5-3-6-10-14/h3,5-6,8-10,19H,1-2,4,7,11-12H2,(H,17,18)/b13-8-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	360	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Inhibition of HDAC in human HeLa cell nuclear extract by fluorescence assay				Bioorg Med Chem 18: 605-11 (2010) Article DOI: 10.1016/j.bmc.2009.12.005 BindingDB Entry DOI: 10.7270/Q20C4ZMK
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051690 (CHEMBL3311137) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C51H63N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h8-26,32-33,39-43H,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	420	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of fMLP-induced calcium mobilization incubated for 5 mins p...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
Histone deacetylase (Homo sapiens (Human))	BDBM50481611 (CHEMBL599968) Show SMILES F\C(CS)=C/CCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H18FNOS/c15-12(11-18)7-3-1-6-10-14(17)16-13-8-4-2-5-9-13/h2,4-5,7-9,18H,1,3,6,10-11H2,(H,16,17)/b12-7-	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Inhibition of HDAC in human HeLa cell nuclear extract by fluorescence assay				Bioorg Med Chem 18: 605-11 (2010) Article DOI: 10.1016/j.bmc.2009.12.005 BindingDB Entry DOI: 10.7270/Q20C4ZMK
					More data for this Ligand-Target Pair
Histone deacetylase (Homo sapiens (Human))	BDBM19149 (CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...) Show SMILES ONC(=O)CCCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Inhibition of HDAC in human HeLa cell nuclear extract by fluorescence assay				Bioorg Med Chem 18: 605-11 (2010) Article DOI: 10.1016/j.bmc.2009.12.005 BindingDB Entry DOI: 10.7270/Q20C4ZMK
					More data for this Ligand-Target Pair				3D Structure (crystal)
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051608 (CHEMBL3311030) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C44H59N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h8-22,28-29,33-37H,23-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of fMLP-induced calcium mobilization incubated for 5 mins p...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051624 (CHEMBL3311293) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](COC(C)(C)C)C(O)=O |r| Show InChI InChI=1S/C42H63N5O9/c1-26(2)21-30(44-38(51)33(24-29-19-15-12-16-20-29)47-40(54)56-42(8,9)10)35(48)45-32(23-28-17-13-11-14-18-28)37(50)43-31(22-27(3)4)36(49)46-34(39(52)53)25-55-41(5,6)7/h11-20,26-27,30-34H,21-25H2,1-10H3,(H,43,50)(H,44,51)(H,45,48)(H,46,49)(H,47,54)(H,52,53)/t30-,31-,32+,33+,34+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051631 (CHEMBL3311292) Show SMILES CC(C)C[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(O)=O |r| Show InChI InChI=1S/C41H61N5O8/c1-25(2)20-30(43-38(50)33(24-29-18-14-11-15-19-29)46-40(53)54-41(7,8)9)35(47)44-32(23-28-16-12-10-13-17-28)37(49)42-31(21-26(3)4)36(48)45-34(39(51)52)22-27(5)6/h10-19,25-27,30-34H,20-24H2,1-9H3,(H,42,49)(H,43,50)(H,44,47)(H,45,48)(H,46,53)(H,51,52)/t30-,31-,32+,33+,34+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051639 (CHEMBL3309281) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O |r| Show InChI InChI=1S/C40H59N5O8/c1-24(2)20-29(41-36(48)32(23-28-18-14-11-15-19-28)44-39(52)53-40(7,8)9)34(46)43-31(22-27-16-12-10-13-17-27)35(47)42-30(21-25(3)4)37(49)45-33(26(5)6)38(50)51/h10-19,24-26,29-33H,20-23H2,1-9H3,(H,41,48)(H,42,47)(H,43,46)(H,44,52)(H,45,49)(H,50,51)/t29-,30-,31+,32+,33+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051654 (CHEMBL3311291) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C51H63N5O9/c1-32(2)27-39(53-48(61)42(29-34-17-11-8-12-18-34)56-50(64)65-51(5,6)7)45(58)54-41(30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h8-26,32-33,39-43H,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051680 (CHEMBL3311290) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CCCCNC(=O)OC(C)(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C46H70N6O10/c1-29(2)25-34(50-41(56)36(27-31-19-13-11-14-20-31)52-44(60)62-46(8,9)10)39(54)48-33(23-17-18-24-47-43(59)61-45(5,6)7)38(53)49-35(26-30(3)4)40(55)51-37(42(57)58)28-32-21-15-12-16-22-32/h11-16,19-22,29-30,33-37H,17-18,23-28H2,1-10H3,(H,47,59)(H,48,54)(H,49,53)(H,50,56)(H,51,55)(H,52,60)(H,57,58)/t33-,34+,35+,36-,37-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051681 (CHEMBL3311289) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC(=O)OC(C)(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C43H63N5O10/c1-26(2)21-30(44-38(52)32(23-28-17-13-11-14-18-28)48-41(56)58-43(8,9)10)36(50)46-33(25-35(49)57-42(5,6)7)39(53)45-31(22-27(3)4)37(51)47-34(40(54)55)24-29-19-15-12-16-20-29/h11-20,26-27,30-34H,21-25H2,1-10H3,(H,44,52)(H,45,53)(H,46,50)(H,47,51)(H,48,56)(H,54,55)/t30-,31-,32+,33+,34+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051682 (CHEMBL3311288) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H]([C@@H](C)OC(C)(C)C)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C43H65N5O9/c1-26(2)22-31(36(49)46-34(40(53)54)25-30-20-16-13-17-21-30)45-39(52)35(28(5)56-42(6,7)8)48-38(51)32(23-27(3)4)44-37(50)33(24-29-18-14-12-15-19-29)47-41(55)57-43(9,10)11/h12-21,26-28,31-35H,22-25H2,1-11H3,(H,44,50)(H,45,52)(H,46,49)(H,47,55)(H,48,51)(H,53,54)/t28-,31-,32-,33+,34+,35+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	830	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051683 (CHEMBL3311144) Show SMILES CSCC[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C40H59N5O8S/c1-25(2)21-30(43-37(49)32(23-27-15-11-9-12-16-27)45-39(52)53-40(5,6)7)35(47)41-29(19-20-54-8)34(46)42-31(22-26(3)4)36(48)44-33(38(50)51)24-28-17-13-10-14-18-28/h9-18,25-26,29-33H,19-24H2,1-8H3,(H,41,47)(H,42,46)(H,43,49)(H,44,48)(H,45,52)(H,50,51)/t29-,30+,31+,32-,33-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051684 (CHEMBL3311143) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC1CCCCC1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C44H65N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h9-10,13-16,19-22,28-30,33-37H,8,11-12,17-18,23-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051685 (CHEMBL3311142) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C41H61N5O8/c1-25(2)20-30(35(47)43-32(22-27(5)6)37(49)45-34(39(51)52)24-29-18-14-11-15-19-29)42-36(48)31(21-26(3)4)44-38(50)33(23-28-16-12-10-13-17-28)46-40(53)54-41(7,8)9/h10-19,25-27,30-34H,20-24H2,1-9H3,(H,42,48)(H,43,47)(H,44,50)(H,45,49)(H,46,53)(H,51,52)/t30-,31+,32+,33-,34-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051686 (CHEMBL3311141) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C40H59N5O8/c1-24(2)20-29(34(46)43-32(38(50)51)23-28-18-14-11-15-19-28)42-37(49)33(26(5)6)45-36(48)30(21-25(3)4)41-35(47)31(22-27-16-12-10-13-17-27)44-39(52)53-40(7,8)9/h10-19,24-26,29-33H,20-23H2,1-9H3,(H,41,47)(H,42,49)(H,43,46)(H,44,52)(H,45,48)(H,50,51)/t29-,30-,31+,32+,33+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051687 (CHEMBL3311140) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CCCCNC(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C48H66N6O9/c1-31(2)27-37(50-42(56)36(54-47(62)63-48(5,6)7)25-17-18-26-49-41(55)35-23-15-10-16-24-35)43(57)52-39(29-33-19-11-8-12-20-33)45(59)51-38(28-32(3)4)44(58)53-40(46(60)61)30-34-21-13-9-14-22-34/h8-16,19-24,31-32,36-40H,17-18,25-30H2,1-7H3,(H,49,55)(H,50,56)(H,51,59)(H,52,57)(H,53,58)(H,54,62)(H,60,61)/t36-,37+,38+,39-,40-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051688 (CHEMBL3311139) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CCCCNC(=O)C1CCCCC1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C48H72N6O9/c1-31(2)27-37(50-42(56)36(54-47(62)63-48(5,6)7)25-17-18-26-49-41(55)35-23-15-10-16-24-35)43(57)52-39(29-33-19-11-8-12-20-33)45(59)51-38(28-32(3)4)44(58)53-40(46(60)61)30-34-21-13-9-14-22-34/h8-9,11-14,19-22,31-32,35-40H,10,15-18,23-30H2,1-7H3,(H,49,55)(H,50,56)(H,51,59)(H,52,57)(H,53,58)(H,54,62)(H,60,61)/t36-,37+,38+,39-,40-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051689 (CHEMBL3311138) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CCCCN)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C41H62N6O8/c1-26(2)22-31(43-35(48)30(20-14-15-21-42)47-40(54)55-41(5,6)7)36(49)45-33(24-28-16-10-8-11-17-28)38(51)44-32(23-27(3)4)37(50)46-34(39(52)53)25-29-18-12-9-13-19-29/h8-13,16-19,26-27,30-34H,14-15,20-25,42H2,1-7H3,(H,43,48)(H,44,51)(H,45,49)(H,46,50)(H,47,54)(H,52,53)/t30-,31+,32+,33-,34-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051690 (CHEMBL3311137) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C51H63N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h8-26,32-33,39-43H,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051691 (CHEMBL3311136) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1cn(C(=O)OC(C)(C)C)c2ccccc12)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C51H68N6O10/c1-31(2)25-37(53-46(61)40(56-48(64)66-50(5,6)7)29-35-30-57(49(65)67-51(8,9)10)42-24-18-17-23-36(35)42)43(58)54-39(27-33-19-13-11-14-20-33)45(60)52-38(26-32(3)4)44(59)55-41(47(62)63)28-34-21-15-12-16-22-34/h11-24,30-32,37-41H,25-29H2,1-10H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t37-,38-,39+,40+,41+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	69	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051692 (CHEMBL3311135) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1cn(C=O)c2ccccc12)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C47H60N6O9/c1-29(2)22-35(49-44(58)38(52-46(61)62-47(5,6)7)26-33-27-53(28-54)40-21-15-14-20-34(33)40)41(55)50-37(24-31-16-10-8-11-17-31)43(57)48-36(23-30(3)4)42(56)51-39(45(59)60)25-32-18-12-9-13-19-32/h8-21,27-30,35-39H,22-26H2,1-7H3,(H,48,57)(H,49,58)(H,50,55)(H,51,56)(H,52,61)(H,59,60)/t35-,36-,37+,38+,39+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051693 (CHEMBL3311134) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051694 (CHEMBL3311133) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C48H67N5O9/c1-30(2)25-36(50-44(57)39(53-46(60)62-48(8,9)10)28-34-21-23-35(24-22-34)61-47(5,6)7)41(54)51-38(27-32-17-13-11-14-18-32)43(56)49-37(26-31(3)4)42(55)52-40(45(58)59)29-33-19-15-12-16-20-33/h11-24,30-31,36-40H,25-29H2,1-10H3,(H,49,56)(H,50,57)(H,51,54)(H,52,55)(H,53,60)(H,58,59)/t36-,37-,38+,39+,40+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	62	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051695 (CHEMBL3311132) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(Cl)cc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C44H58ClN5O8/c1-27(2)22-33(47-41(54)36(50-43(57)58-44(5,6)7)25-31-18-20-32(45)21-19-31)38(51)48-35(24-29-14-10-8-11-15-29)40(53)46-34(23-28(3)4)39(52)49-37(42(55)56)26-30-16-12-9-13-17-30/h8-21,27-28,33-37H,22-26H2,1-7H3,(H,46,53)(H,47,54)(H,48,51)(H,49,52)(H,50,57)(H,55,56)/t33-,34-,35+,36+,37+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	75	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051696 (CHEMBL3311131) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC1CCCCC1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C44H65N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h8,10-12,15-18,21-22,28-29,31,33-37H,9,13-14,19-20,23-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	66	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051699 (CHEMBL3311130) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](COC(C)(C)C)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C42H63N5O9/c1-26(2)21-30(44-38(51)34(25-55-41(5,6)7)47-40(54)56-42(8,9)10)35(48)45-32(23-28-17-13-11-14-18-28)37(50)43-31(22-27(3)4)36(49)46-33(39(52)53)24-29-19-15-12-16-20-29/h11-20,26-27,30-34H,21-25H2,1-10H3,(H,43,50)(H,44,51)(H,45,48)(H,46,49)(H,47,54)(H,52,53)/t30-,31-,32+,33+,34+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051700 (CHEMBL3311037) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](NC(=O)OC(C)(C)C)[C@@H](C)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C43H65N5O9/c1-26(2)22-31(37(50)47-34(40(53)54)25-30-20-16-13-17-21-30)44-38(51)33(24-29-18-14-12-15-19-29)45-36(49)32(23-27(3)4)46-39(52)35(28(5)56-42(6,7)8)48-41(55)57-43(9,10)11/h12-21,26-28,31-35H,22-25H2,1-11H3,(H,44,51)(H,45,49)(H,46,52)(H,47,50)(H,48,55)(H,53,54)/t28-,31-,32-,33+,34+,35+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051702 (CHEMBL3311036) Show SMILES CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C41H61N5O8/c1-25(2)20-30(42-37(49)32(22-27(5)6)46-40(53)54-41(7,8)9)35(47)44-33(23-28-16-12-10-13-17-28)38(50)43-31(21-26(3)4)36(48)45-34(39(51)52)24-29-18-14-11-15-19-29/h10-19,25-27,30-34H,20-24H2,1-9H3,(H,42,49)(H,43,50)(H,44,47)(H,45,48)(H,46,53)(H,51,52)/t30-,31-,32+,33+,34+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051703 (CHEMBL3311035) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](C)C(O)=O |r| Show InChI InChI=1S/C38H55N5O8/c1-23(2)19-28(32(44)39-25(5)36(48)49)40-34(46)30(21-26-15-11-9-12-16-26)42-33(45)29(20-24(3)4)41-35(47)31(22-27-17-13-10-14-18-27)43-37(50)51-38(6,7)8/h9-18,23-25,28-31H,19-22H2,1-8H3,(H,39,44)(H,40,46)(H,41,47)(H,42,45)(H,43,50)(H,48,49)/t25-,28+,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051704 (CHEMBL3311034) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C41H53N5O8/c1-26(2)22-31(43-38(50)33(24-29-18-12-8-13-19-29)46-40(53)54-41(4,5)6)37(49)44-32(23-28-16-10-7-11-17-28)36(48)42-27(3)35(47)45-34(39(51)52)25-30-20-14-9-15-21-30/h7-21,26-27,31-34H,22-25H2,1-6H3,(H,42,48)(H,43,50)(H,44,49)(H,45,47)(H,46,53)(H,51,52)/t27-,31+,32-,33-,34-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	420	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051705 (CHEMBL3311033) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C38H55N5O8/c1-23(2)19-28(41-35(47)30(21-26-15-11-9-12-16-26)43-37(50)51-38(6,7)8)33(45)39-25(5)32(44)40-29(20-24(3)4)34(46)42-31(36(48)49)22-27-17-13-10-14-18-27/h9-18,23-25,28-31H,19-22H2,1-8H3,(H,39,45)(H,40,44)(H,41,47)(H,42,46)(H,43,50)(H,48,49)/t25-,28+,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	280	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051706 (CHEMBL3311032) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C41H53N5O8/c1-26(2)22-31(37(49)45-34(39(51)52)25-30-20-14-9-15-21-30)44-38(50)32(23-28-16-10-7-11-17-28)43-35(47)27(3)42-36(48)33(24-29-18-12-8-13-19-29)46-40(53)54-41(4,5)6/h7-21,26-27,31-34H,22-25H2,1-6H3,(H,42,48)(H,43,47)(H,44,50)(H,45,49)(H,46,53)(H,51,52)/t27-,31+,32-,33-,34-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051708 (CHEMBL3311031) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](C)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C38H55N5O8/c1-23(2)19-28(40-32(44)25(5)39-37(50)51-38(6,7)8)33(45)42-30(21-26-15-11-9-12-16-26)35(47)41-29(20-24(3)4)34(46)43-31(36(48)49)22-27-17-13-10-14-18-27/h9-18,23-25,28-31H,19-22H2,1-8H3,(H,39,50)(H,40,44)(H,41,47)(H,42,45)(H,43,46)(H,48,49)/t25-,28+,29+,30-,31-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051608 (CHEMBL3311030) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r| Show InChI InChI=1S/C44H59N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h8-22,28-29,33-37H,23-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	230	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2/fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50490560 (CHEMBL2336646) Show SMILES CSCC[C@H](NC=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@]1(C[C@@H]1c1ccccc1)C(O)=O |r| Show InChI InChI=1S/C22H31N3O5S/c1-14(2)11-18(24-19(27)17(23-13-26)9-10-31-3)20(28)25-22(21(29)30)12-16(22)15-7-5-4-6-8-15/h4-8,13-14,16-18H,9-12H2,1-3H3,(H,23,26)(H,24,27)(H,25,28)(H,29,30)/t16-,17+,18+,22-/m1/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	250	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Agonist activity at FPR1/FPR2 receptor in human neutrophils assessed as induction of superoxide radical generation by spectrophotometric analysis				Bioorg Med Chem 21: 668-75 (2013) Article DOI: 10.1016/j.bmc.2012.11.046 BindingDB Entry DOI: 10.7270/Q2K64N1S
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2/fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50490561 (CHEMBL2336648) Show SMILES COC(=O)[C@@]1(C[C@H]1c1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC=O |r| Show InChI InChI=1S/C23H33N3O5S/c1-15(2)12-19(25-20(28)18(24-14-27)10-11-32-4)21(29)26-23(22(30)31-3)13-17(23)16-8-6-5-7-9-16/h5-9,14-15,17-19H,10-13H2,1-4H3,(H,24,27)(H,25,28)(H,26,29)/t17-,18-,19-,23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	21	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Agonist activity at FPR1/FPR2 receptor in human neutrophils assessed as induction of chemotaxis after 60 mins				Bioorg Med Chem 21: 668-75 (2013) Article DOI: 10.1016/j.bmc.2012.11.046 BindingDB Entry DOI: 10.7270/Q2K64N1S
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2/fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50490562 (CHEBI:5158 | CHEMBL285518) Show SMILES COC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC=O |r| Show InChI InChI=1S/C22H33N3O5S/c1-15(2)12-18(24-20(27)17(23-14-26)10-11-31-4)21(28)25-19(22(29)30-3)13-16-8-6-5-7-9-16/h5-9,14-15,17-19H,10-13H2,1-4H3,(H,23,26)(H,24,27)(H,25,28)/t17-,18-,19-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	2.5	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Agonist activity at FPR1/FPR2 receptor in human neutrophils assessed as induction of chemotaxis after 60 mins				Bioorg Med Chem 21: 668-75 (2013) Article DOI: 10.1016/j.bmc.2012.11.046 BindingDB Entry DOI: 10.7270/Q2K64N1S
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2/fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50490562 (CHEBI:5158 | CHEMBL285518) Show SMILES COC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC=O |r| Show InChI InChI=1S/C22H33N3O5S/c1-15(2)12-18(24-20(27)17(23-14-26)10-11-31-4)21(28)25-19(22(29)30-3)13-16-8-6-5-7-9-16/h5-9,14-15,17-19H,10-13H2,1-4H3,(H,23,26)(H,24,27)(H,25,28)/t17-,18-,19-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	16	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Agonist activity at FPR1/FPR2 receptor in human neutrophils assessed as induction of superoxide radical generation by spectrophotometric analysis				Bioorg Med Chem 21: 668-75 (2013) Article DOI: 10.1016/j.bmc.2012.11.046 BindingDB Entry DOI: 10.7270/Q2K64N1S
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2/fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50490563 (CHEMBL2336649) Show SMILES COC(=O)[C@@]1(C[C@@H]1c1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC=O |r| Show InChI InChI=1S/C23H33N3O5S/c1-15(2)12-19(25-20(28)18(24-14-27)10-11-32-4)21(29)26-23(22(30)31-3)13-17(23)16-8-6-5-7-9-16/h5-9,14-15,17-19H,10-13H2,1-4H3,(H,24,27)(H,25,28)(H,26,29)/t17-,18+,19+,23+/m1/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	14	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Agonist activity at FPR1/FPR2 receptor in human neutrophils assessed as induction of chemotaxis after 60 mins				Bioorg Med Chem 21: 668-75 (2013) Article DOI: 10.1016/j.bmc.2012.11.046 BindingDB Entry DOI: 10.7270/Q2K64N1S
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2/fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50490564 (CHEMBL2336647) Show SMILES COC(=O)[C@]1(C[C@H]1c1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC=O |r| Show InChI InChI=1S/C23H33N3O5S/c1-15(2)12-19(25-20(28)18(24-14-27)10-11-32-4)21(29)26-23(22(30)31-3)13-17(23)16-8-6-5-7-9-16/h5-9,14-15,17-19H,10-13H2,1-4H3,(H,24,27)(H,25,28)(H,26,29)/t17-,18-,19-,23+/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	4.70	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Agonist activity at FPR1/FPR2 receptor in human neutrophils assessed as induction of chemotaxis after 60 mins				Bioorg Med Chem 21: 668-75 (2013) Article DOI: 10.1016/j.bmc.2012.11.046 BindingDB Entry DOI: 10.7270/Q2K64N1S
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051622 (CHEMBL3311294) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)OC(C)(C)C)C(O)=O |r| Show InChI InChI=1S/C43H65N5O9/c1-26(2)22-31(44-38(51)34(25-30-20-16-13-17-21-30)47-41(55)57-43(9,10)11)36(49)46-33(24-29-18-14-12-15-19-29)37(50)45-32(23-27(3)4)39(52)48-35(40(53)54)28(5)56-42(6,7)8/h12-21,26-28,31-35H,22-25H2,1-11H3,(H,44,51)(H,45,50)(H,46,49)(H,47,55)(H,48,52)(H,53,54)/t28-,31-,32-,33+,34+,35+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051616 (CHEMBL3311295) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC1CCCCC1)C(O)=O |r| Show InChI InChI=1S/C44H65N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h8-9,11-14,17-20,28-29,32-37H,10,15-16,21-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	77	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051614 (CHEMBL3311296) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccc(OC(C)(C)C)cc1)C(O)=O |r| Show InChI InChI=1S/C48H67N5O9/c1-30(2)25-36(50-44(57)39(28-33-19-15-12-16-20-33)53-46(60)62-48(8,9)10)41(54)51-38(27-32-17-13-11-14-18-32)43(56)49-37(26-31(3)4)42(55)52-40(45(58)59)29-34-21-23-35(24-22-34)61-47(5,6)7/h11-24,30-31,36-40H,25-29H2,1-10H3,(H,49,56)(H,50,57)(H,51,54)(H,52,55)(H,53,60)(H,58,59)/t36-,37-,38+,39+,40+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	68	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051613 (CHEMBL3311297) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051612 (CHEMBL3311298) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1cn(C(=O)OC(C)(C)C)c2ccccc12)C(O)=O |r| Show InChI InChI=1S/C51H68N6O10/c1-31(2)25-37(53-46(61)40(28-34-21-15-12-16-22-34)56-48(64)66-50(5,6)7)43(58)54-39(27-33-19-13-11-14-20-33)45(60)52-38(26-32(3)4)44(59)55-41(47(62)63)29-35-30-57(49(65)67-51(8,9)10)42-24-18-17-23-36(35)42/h11-24,30-32,37-41H,25-29H2,1-10H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t37-,38-,39+,40+,41+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM50051611 (CHEMBL3311299) Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccc(cc1)C(=O)c1ccccc1)C(O)=O |r| Show InChI InChI=1S/C51H63N5O9/c1-32(2)27-39(53-48(61)42(30-35-19-13-9-14-20-35)56-50(64)65-51(5,6)7)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37/h8-26,32-33,39-43H,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a
Saga University Curated by ChEMBL					Assay Description Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...				Bioorg Med Chem 22: 3824-8 (2014) Article DOI: 10.1016/j.bmc.2014.06.048 BindingDB Entry DOI: 10.7270/Q28S4RK8
					More data for this Ligand-Target Pair

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