(-)-noradrenaline


SMILES NC[C@@H](c1ccc(c(c1)O)O)O
InChIKey SFLSHLFXELFNJZ-QMMMGPOBSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 4
Rotatable bonds 2
Molecular weight (Da) 169.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Endogenous
Approved drug Yes

Database connections

Structure pdb 7EJ0
Ligand site mutations α1A α1B α2A α2B β2 β3 D4

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α1A ADA1A Human Adrenoceptors A pKi 4.8 5.6 6.4 Guide to Pharmacology
α1B ADA1B Human Adrenoceptors A pKi 3.8 5.0 6.2 Guide to Pharmacology
α1D ADA1D Human Adrenoceptors A pKi 5.5 6.45 7.4 Guide to Pharmacology
α2A ADA2A Human Adrenoceptors A pKi 3.6 5.5 7.4 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pKi 3.5 4.75 6.0 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pKi 4.5 5.65 6.8 Guide to Pharmacology
α1D ADA1D Rat Adrenoceptors A pKi 6.3 6.3 6.3 Guide to Pharmacology
β1 ADRB1 Human Adrenoceptors A pKi 5.5 5.75 6.0 Guide to Pharmacology
β2 ADRB2 Human Adrenoceptors A pKi 4.6 5.0 5.4 Guide to Pharmacology
β3 ADRB3 Human Adrenoceptors A pKi 4.7 5.5 6.3 Guide to Pharmacology
β3 ADRB3 Mouse Adrenoceptors A pKi 3.8 3.8 3.8 Guide to Pharmacology
β3 ADRB3 Rat Adrenoceptors A pKi 4.2 4.2 4.2 Guide to Pharmacology
α2C ADA2C Mouse Adrenoceptors A pKi 6.19 6.19 6.19 ChEMBL
α2A ADA2A Mouse Adrenoceptors A pKi 5.24 5.24 5.24 ChEMBL
α2B ADA2B Rat Adrenoceptors A pKi 7.11 7.11 7.11 ChEMBL
β2 ADRB2 Rat Adrenoceptors A pKi 5.38 5.38 5.38 ChEMBL
β2 ADRB2 Bovine Adrenoceptors A pKi 5.22 5.22 5.22 ChEMBL
α1B ADA1B Golden hamster Adrenoceptors A pKi 6.58 6.58 6.58 ChEMBL
β2 ADRB2 Dog Adrenoceptors A pKi 4.57 4.94 5.3 ChEMBL
α1A ADA1A Bovine Adrenoceptors A pKi 6.35 6.35 6.35 ChEMBL
β1 ADRB1 Rat Adrenoceptors A pKi 4.58 5.94 6.9 ChEMBL
β1 B0FL73 Guinea pig Adrenoceptors A pKi 6.4 6.4 6.4 ChEMBL
α1D ADA1D Rat Adrenoceptors A pKi 7.65 7.65 7.65 ChEMBL
α1B ADA1B Human Adrenoceptors A pKi 4.69 4.69 4.69 ChEMBL
α1A ADA1A Rat Adrenoceptors A pKi 6.55 6.55 6.55 ChEMBL
α2C ADA2C Human Adrenoceptors A pKi 7.2 7.2 7.2 ChEMBL
α1A ADA1A Human Adrenoceptors A pKi 5.82 5.82 5.82 ChEMBL
α2A ADA2A Human Adrenoceptors A pKi 7.18 7.18 7.18 ChEMBL
D1 DRD1 Human Dopamine A pKd 4.3 4.3 4.3 ChEMBL
β2 ADRB2 Human Adrenoceptors A pKd 5.4 5.4 5.4 ChEMBL
β2 ADRB2 Human Adrenoceptors A pKi 4.01 4.75 5.48 ChEMBL
D2 DRD2 Human Dopamine A pKi 5.89 5.89 5.89 ChEMBL
α1B ADA1B Human Adrenoceptors A pKi 8.33 8.33 8.33 Drug Central
α1D ADA1D Human Adrenoceptors A pKi 8.13 8.13 8.13 Drug Central
α2A ADA2A Human Adrenoceptors A pKi 8.14 8.14 8.14 Drug Central
α2B ADA2B Human Adrenoceptors A pKi 8.19 8.19 8.19 Drug Central
α2C ADA2C Human Adrenoceptors A pKi 8.14 8.14 8.14 Drug Central
β1 ADRB1 Human Adrenoceptors A pKi 8.22 8.22 8.22 Drug Central
β2 ADRB2 Human Adrenoceptors A pKd 8.27 8.27 8.27 Drug Central
β3 ADRB3 Human Adrenoceptors A pKi 8.27 8.27 8.27 Drug Central
D2 DRD2 Human Dopamine A pKi 8.23 8.23 8.23 Drug Central
μ OPRM Rat Opioid A pKi 8.31 8.31 8.31 Drug Central
β2 ADRB2 Bovine Adrenoceptors A pKi 8.28 8.28 8.28 Drug Central
α2B ADA2B Rat Adrenoceptors A pKi 8.15 8.15 8.15 Drug Central
α2C ADA2C Mouse Adrenoceptors A pKi 8.21 8.21 8.21 Drug Central
β2 ADRB2 Rat Adrenoceptors A pKi 8.27 8.27 8.27 Drug Central
α2A ADA2A Mouse Adrenoceptors A pKi 8.28 8.28 8.28 Drug Central
α1B ADA1B Golden hamster Adrenoceptors A pKi 8.18 8.18 8.18 Drug Central
α1A ADA1A Bovine Adrenoceptors A pKi 8.2 8.2 8.2 Drug Central
β2 ADRB2 Dog Adrenoceptors A pKi 8.28 8.28 8.28 Drug Central
β1 B0FL73 Guinea pig Adrenoceptors A pKi 8.19 8.19 8.19 Drug Central
α1A ADA1A Human Adrenoceptors A pKi 8.24 8.24 8.24 Drug Central
D1 DRD1 Human Dopamine A pKd 8.37 8.37 8.37 Drug Central
β1 ADRB1 Rat Adrenoceptors A pKi 8.16 8.16 8.16 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α1A ADA1A Human Adrenoceptors A pEC50 5.5 7.05 8.6 Guide to Pharmacology
α1B ADA1B Human Adrenoceptors A pEC50 5.9 7.55 9.2 Guide to Pharmacology
α1D ADA1D Human Adrenoceptors A pEC50 6.6 7.2 7.8 Guide to Pharmacology
α2A ADA2A Human Adrenoceptors A pEC50 6.566666666666666 6.57 6.57 Guide to Pharmacology
α2A ADA2A Human Adrenoceptors A pIC50 6.6 6.6 6.6 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pEC50 7.35 7.35 7.35 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pIC50 7.8 7.8 7.8 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pEC50 6.02 7.0 6.6 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pIC50 6.5 7.55 8.6 Guide to Pharmacology
β1 ADRB1 Human Adrenoceptors A pEC50 7.9 7.9 7.9 Guide to Pharmacology
β2 ADRB2 Human Adrenoceptors A pEC50 6.4 6.4 6.4 Guide to Pharmacology
β3 ADRB3 Human Adrenoceptors A pEC50 7.2 7.2 7.2 Guide to Pharmacology
β3 ADRB3 Rat Adrenoceptors A pEC50 4.0 4.9 5.8 ChEMBL
β1 B0FL73 Guinea pig Adrenoceptors A pEC50 5.0 6.33 7.52 ChEMBL
β2 ADRB2 Guinea pig Adrenoceptors A pEC50 4.52 5.59 6.67 ChEMBL
α1D ADA1D Rat Adrenoceptors A pEC50 7.92 7.92 7.92 ChEMBL
α1B ADA1B Rat Adrenoceptors A pEC50 4.99 4.99 4.99 ChEMBL
α1A ADA1A Rat Adrenoceptors A pEC50 5.93 5.93 5.93 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.55 4.85 5.15 ChEMBL
α2B ADA2B Human Adrenoceptors A pEC50 7.21 7.21 7.21 ChEMBL
α2C ADA2C Human Adrenoceptors A pEC50 6.1 6.1 6.1 ChEMBL
β3 ADRB3 Human Adrenoceptors A pEC50 8.2 8.23 8.26 ChEMBL
α1A ADA1A Human Adrenoceptors A pEC50 5.66 7.25 8.04 ChEMBL
α2A ADA2A Human Adrenoceptors A pEC50 6.43 6.64 6.96 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.5 5.17 5.5 ChEMBL