BDBM50517308 CHEMBL4579650

SMILES: [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO

InChI Key: InChIKey=AWXOZEOHMQXOAJ-NQNJJODYSA-N

Data: 7 KI

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 7 hits for monomerid = 50517308   

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
Adenosine A1 receptor (Mus musculus)	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Displacement of [3H]N6-R-phenylisopropyladenosine from mouse A1A adenosine receptor expressed in CHO cell membranes after 60 mins by scintillation pr...				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair
Adenosine receptor A1 (Homo sapiens (Human))	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Displacement of [3H]N6-R-phenylisopropyladenosine from human A1A adenosine receptor expressed in CHO cell membranes after 60 mins by scintillation pr...				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Homo sapiens (Human))	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	127	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Displacement of [125I]N6-(4-amino-3-iodobenzyl)adenosine-5-N-methyluronamide from human A3A adenosine receptor expressed in CHO cell membranes after ...				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair
Adenosine receptor A3 (Mus musculus)	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	447	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Displacement of [125I]N6-(4-amino-3-iodobenzyl)adenosine-5-N-methyluronamide from mouse A3A adenosine receptor expressed in CHO cell membranes after ...				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2B (Homo sapiens (Human))	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	718	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Inhibition of 5HT2B (unknown origin)				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	2.63E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Inhibition of KOR (unknown origin)				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair
Adenosine receptor A2a (Homo sapiens (Human))	BDBM50517308 (CHEMBL4579650) Show SMILES [H][C@]12C[C@]1([C@@H](O)[C@@H](O)[C@@H]2n1cnc2c(N[C@H]3C[C@@]4([H])CC[C@]3([H])C4)nc(Cl)nc12)C(=O)NCCO |r,TLB:14:15:20.19:23| Show InChI InChI=1S/C21H27ClN6O4/c22-20-26-17(25-12-6-9-1-2-10(12)5-9)13-18(27-20)28(8-24-13)14-11-7-21(11,16(31)15(14)30)19(32)23-3-4-29/h8-12,14-16,29-31H,1-7H2,(H,23,32)(H,25,26,27)/t9-,10+,11+,12-,14+,15-,16-,21-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Wisconsin Curated by ChEMBL					Assay Description Displacement of [3H]2-[p-(2-carboxyethyl)phenylethylamino]-5-N-ethylcarboxamidoadenosine from human A2A adenosine receptor expressed in HEK293 cell m...				J Med Chem 62: 1502-1522 (2019) Article DOI: 10.1021/acs.jmedchem.8b01662
					More data for this Ligand-Target Pair