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Name | Beta-1 adrenergic receptor |
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Species | Homo sapiens (Human) |
Gene | ADRB1 |
Synonym | Adrenergic receptor beta 1 Adrb-1 ADRB1R adrenergic receptor beta 1-AR [ Show all ] |
Disease | Heart failure; Cardiogenic shock Heart failure Glaucoma Diabetes Coronary artery disease [ Show all ] |
Length | 477 |
Amino acid sequence | MGAGVLVLGASEPGNLSSAAPLPDGAATAARLLVPASPPASLLPPASESPEPLSQQWTAGMGLLMALIVLLIVAGNVLVIVAIAKTPRLQTLTNLFIMSLASADLVMGLLVVPFGATIVVWGRWEYGSFFCELWTSVDVLCVTASIETLCVIALDRYLAITSPFRYQSLLTRARARGLVCTVWAISALVSFLPILMHWWRAESDEARRCYNDPKCCDFVTNRAYAIASSVVSFYVPLCIMAFVYLRVFREAQKQVKKIDSCERRFLGGPARPPSPSPSPVPAPAPPPGPPRPAAAAATAPLANGRAGKRRPSRLVALREQKALKTLGIIMGVFTLCWLPFFLANVVKAFHRELVPDRLFVFFNWLGYANSAFNPIIYCRSPDFRKAFQRLLCCARRAARRRHATHGDRPRASGCLARPGPPPSPGAASDDDDDDVVGATPPARLLEPWAGCNGGAAADSDSSLDEPCRPGFASESKV |
UniProt | P08588 |
Protein Data Bank | N/A |
GPCR-HGmod model | P08588 |
3D structure model | This predicted structure model is from GPCR-EXP P08588. |
BioLiP | N/A |
Therapeutic Target Database | T44068 |
ChEMBL | CHEMBL213 |
IUPHAR | 28 |
DrugBank | BE0000172 |
Name | isoproterenol |
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Molecular formula | C11H17NO3 |
IUPAC name | 4-[1-hydroxy-2-(propan-2-ylamino)ethyl]benzene-1,2-diol |
Molecular weight | 211.261 |
Hydrogen bond acceptor | 4 |
Hydrogen bond donor | 4 |
XlogP | -0.6 |
Synonyms | Isupren WIN 5162 KBioGR_000427 LS-42868 NCGC00015558-04 [ Show all ] |
Inchi Key | JWZZKOKVBUJMES-UHFFFAOYSA-N |
Inchi ID | InChI=1S/C11H17NO3/c1-7(2)12-6-11(15)8-3-4-9(13)10(14)5-8/h3-5,7,11-15H,6H2,1-2H3 |
PubChem CID | 3779 |
ChEMBL | CHEMBL434 |
IUPHAR | 536 |
BindingDB | 25392 |
DrugBank | DB01064 |
Structure | |
Lipinski's druglikeness | This ligand satisfies Lipinski's rule of five. |
Parameter | Value | Reference | Database source |
---|---|---|---|
N/A | N/A | DrugBank | |
EC50 | 0.084 nM | PMID18307290, PMID15603933, PMID18651730, PMID18553954 | BindingDB |
EC50 | 0.084 nM | PMID18307290, PMID15603933, PMID18752946, PMID18651730, PMID18553954 | BindingDB,ChEMBL |
EC50 | 0.84 nM | PMID19366244 | BindingDB |
EC50 | 0.84 nM | PMID19366244 | ChEMBL |
EC50 | 1.0 nM | PMID16640337, PMID11806709 | BindingDB,ChEMBL |
EC50 | 7.9 nM | PMID19317397, PMID21696967, PMID21925889, PMID20462258 | BindingDB |
EC50 | 7.943 nM | PMID19317397, PMID21696967, PMID21925889, PMID20462258 | ChEMBL |
EC50 | 12.0 nM | PMID19232786, PMID19581100 | BindingDB,ChEMBL |
EC50 | 100.0 nM | PMID19362005 | BindingDB,ChEMBL |
EC50 | 1000.0 nM | PMID19581100 | BindingDB,ChEMBL |
Emax | 109.0 % | PMID16640337, PMID11806709 | ChEMBL |
IA | 100.0 - | PMID10691685 | ChEMBL |
IC50 | 333.0 nM | DrugMatrix in vitro pharmacology data | ChEMBL |
Intrinsic activity | 1.0 - | PMID19232786 | ChEMBL |
Intrinsic activity | 100.0 - | PMID10377236 | ChEMBL |
Ki | 100.0 - 251.189 nM | PMID8982677, PMID2849109 | IUPHAR |
Ki | 193.0 nM | DrugMatrix in vitro pharmacology data | ChEMBL |
Ki | 224.0 nM | PMID14730417 | BindingDB |
Ki | 1584.89 nM | PMID10377236 | ChEMBL |
pK | 8.81 - | PMID10691685 | ChEMBL |
pKact | 8.75 - | PMID10377236 | ChEMBL |
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