(-)-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
Physiological/Surrogate Endogenous
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α2A ADA2A Human Adrenoceptors A pKi 3.6 5.5 7.4 Guide to Pharmacology
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
α1D ADA1D Rat Adrenoceptors A pKi 6.3 6.3 6.3 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
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 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 Rat Adrenoceptors A pKi 5.38 5.38 5.38 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
α1D ADA1D Human Adrenoceptors A pKi 5.48 5.93 6.37 ChEMBL
α2B ADA2B Human Adrenoceptors A pKi 6.63 6.63 6.63 ChEMBL
α2C ADA2C Human Adrenoceptors A pKi 6.41 6.8 7.2 ChEMBL
β1 ADRB1 Human Adrenoceptors A pKi 6.38 6.38 6.38 ChEMBL
α1A ADA1A Human Adrenoceptors A pKi 4.81 5.31 5.82 ChEMBL
α2A ADA2A Human Adrenoceptors A pKi 5.24 6.21 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
D3 DRD3 Human Dopamine A pKi 6.35 6.35 6.35 ChEMBL
D2 DRD2 Human Dopamine A pKi 5.89 5.89 5.89 ChEMBL
β2 ADRB2 Human Adrenoceptors A pKd 8.27 8.27 8.27 Drug Central
D1 DRD1 Human Dopamine A pKd 8.37 8.37 8.37 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
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
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
β1 ADRB1 Rat Adrenoceptors A pKi 8.16 8.16 8.16 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
α1B ADA1B Human Adrenoceptors A pKi 8.33 8.33 8.33 Drug Central
μ OPRM Rat Opioid A pKi 8.31 8.31 8.31 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
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
α1A ADA1A Human Adrenoceptors A pEC50 7.7 8.15 8.6 Guide to Pharmacology
α1B ADA1B Human Adrenoceptors A pEC50 9.2 9.2 9.2 Guide to Pharmacology
α1D ADA1D Human Adrenoceptors A pEC50 7.8 7.8 7.8 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
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 6.56 7.05 7.21 ChEMBL
α2C ADA2C Human Adrenoceptors A pEC50 6.1 6.15 6.35 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 6.75 7.52 ChEMBL
β2 ADRB2 Human Adrenoceptors A pEC50 5.03 5.03 5.03 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.5 5.17 5.5 ChEMBL
α1B ADA1B Rat Adrenoceptors A pEC50 4.99 4.99 4.99 ChEMBL