clonidine


SMILES Clc1cccc(c1NC1=NCCN1)Cl
InChIKey GJSURZIOUXUGAL-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 2
Rotatable bonds 1
Molecular weight (Da) 229.0

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α1D ADA1D Human Adrenoceptors A pKi 5.6 5.6 5.6 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pKi 6.3 7.9 9.5 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pKi 6.0 6.9 7.8 Guide to Pharmacology
α1D ADA1D Rat Adrenoceptors A pKi 6.9 6.9 6.9 Guide to Pharmacology
α2B ADA2B Rat Adrenoceptors A pKi 6.8 7.65 8.08 ChEMBL
α2A ADA2A Rat Adrenoceptors A pKi 6.07 8.3 9.41 ChEMBL
β1 B0FL73 Guinea pig Adrenoceptors A pKd 4.2 4.3 4.4 ChEMBL
α1B ADA1B Rat Adrenoceptors A pKi 5.99 5.99 5.99 ChEMBL
α1A ADA1A Rat Adrenoceptors A pKd 6.59 6.59 6.59 ChEMBL
α1A ADA1A Rat Adrenoceptors A pKi 6.82 6.82 6.82 ChEMBL
α1D ADA1D Human Adrenoceptors A pKi 6.22 6.22 6.22 ChEMBL
α2B ADA2B Human Adrenoceptors A pKi 7.42 7.71 8.21 ChEMBL
α2C ADA2C Human Adrenoceptors A pKi 6.8 7.42 8.03 ChEMBL
α1A ADA1A Human Adrenoceptors A pKi 6.01 6.15 6.29 ChEMBL
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pKi 5.51 5.51 5.51 ChEMBL
α2A ADA2A Human Adrenoceptors A pKi 6.07 7.66 8.42 ChEMBL
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 5.49 5.49 5.49 ChEMBL
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
α2B ADA2B Human Adrenoceptors A pKi 6.51 7.3 8.14 PDSP Ki database
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
α2A ADA2A Pig Adrenoceptors A pKi 7.07 7.07 7.07 PDSP Ki database
D2 DRD2 Rat Dopamine A pKi 5.0 5.0 5.0 PDSP Ki database
α1D ADA1D Human Adrenoceptors A pKi 6.5 6.7 6.9 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 7.21 7.37 7.5 PDSP Ki database
α2C ADA2C Human Adrenoceptors A pKi 6.3 6.79 7.2 PDSP Ki database
α1D ADA1D Rat Adrenoceptors A pKi 7.0 7.0 7.0 PDSP Ki database
α1B ADA1B Rat Adrenoceptors A pKi 6.5 6.5 6.5 PDSP Ki database
α2A ADA2A Rat Adrenoceptors A pKi 7.6 7.6 7.6 PDSP Ki database
α2A ADA2A Mouse Adrenoceptors A pKi 7.21 7.3 7.39 PDSP Ki database
α1A ADA1A Human Adrenoceptors A pKi 8.19 8.19 8.19 Drug Central
α1B ADA1B Human Adrenoceptors A pKi 8.19 8.19 8.19 Drug Central
α1D ADA1D Human Adrenoceptors A pKi 8.21 8.21 8.21 Drug Central
α2A ADA2A Human Adrenoceptors A pKi 8.07 8.07 8.07 Drug Central
α2B ADA2B Human Adrenoceptors A pKi 8.12 8.12 8.12 Drug Central
α1D ADA1D Rat Adrenoceptors A pKi 8.16 8.16 8.16 Drug Central
α1B ADA1B Rat Adrenoceptors A pKi 8.22 8.22 8.22 Drug Central
α2B ADA2B Rat Adrenoceptors A pKi 8.09 8.09 8.09 Drug Central
α2A ADA2A Rat Adrenoceptors A pKi 8.03 8.03 8.03 Drug Central
β1 B0FL73 Guinea pig Adrenoceptors A pKd 8.36 8.36 8.36 Drug Central
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 8.26 8.26 8.26 Drug Central
α1B ADA1B Human Adrenoceptors A pKi 6.5 6.5 6.5 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 6.7 7.95 9.2 Guide to Pharmacology
α1A ADA1A Rat Adrenoceptors A pKd 8.18 8.18 8.18 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α2B ADA2B Human Adrenoceptors A pEC50 7.7 7.7 7.7 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pIC50 8.6 8.6 8.6 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pEC50 4.64 6.75 6.74 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pIC50 7.5 7.6 7.7 Guide to Pharmacology
α1B ADA1B Rat Adrenoceptors A pIC50 5.73 5.73 5.73 ChEMBL
α1A ADA1A Rat Adrenoceptors A pIC50 6.43 6.43 6.43 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.6 4.65 4.7 ChEMBL
α1D ADA1D Human Adrenoceptors A pIC50 5.92 5.92 5.92 ChEMBL
α2B ADA2B Human Adrenoceptors A pEC50 5.93 6.36 6.78 ChEMBL
α2B ADA2B Human Adrenoceptors A pIC50 7.08 7.08 7.08 ChEMBL
α2C ADA2C Human Adrenoceptors A pEC50 7.24 7.25 7.26 ChEMBL
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pIC50 5.27 5.27 5.27 ChEMBL
α2A ADA2A Human Adrenoceptors A pEC50 7.52 7.79 8.09 ChEMBL
α2A ADA2A Human Adrenoceptors A pIC50 6.55 6.55 6.55 ChEMBL
NPS NPSR1 Human Neuropeptide S A Potency 4.8 4.8 4.8 ChEMBL
α2C ADA2C Human Adrenoceptors A pEC50 8.17 8.17 8.17 Drug Central
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pIC50 8.28 8.28 8.28 Drug Central
α2A ADA2A Bovine Adrenoceptors A pIC50 8.06 8.06 8.06 Drug Central
α1A ADA1A Bovine Adrenoceptors A pEC50 8.15 8.15 8.15 Drug Central
α2A ADA2A Human Adrenoceptors A pEC50 7.666666666666667 7.67 7.67 Guide to Pharmacology
α2A ADA2A Human Adrenoceptors A pIC50 8.2 8.2 8.2 Guide to Pharmacology
α2A ADA2A Bovine Adrenoceptors A pIC50 8.7 8.7 8.7 ChEMBL
α1A ADA1A Bovine Adrenoceptors A pEC50 7.05 7.05 7.05 ChEMBL