(+)-cyclazosin


SMILES COc1cc2nc(nc(c2cc1OC)N)N1CCN([C@@H]2[C@H]1CCCC2)C(=O)c1ccco1
InChIKey XBRXTUGRUXGBPX-DLBZAZTESA-N

Chemical properties

Hydrogen bond acceptors 8
Hydrogen bond donors 1
Rotatable bonds 4
Molecular weight (Da) 437.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Structure pdb 7B6W

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α1A ADA1A Human Adrenoceptors A pKi 7.9 8.4 8.9 Guide to Pharmacology
α1B ADA1B Human Adrenoceptors A pKi 8.7 9.3 9.9 Guide to Pharmacology
α1D ADA1D Human Adrenoceptors A pKi 8.5 9.2 9.9 Guide to Pharmacology
α1D ADA1D Rat Adrenoceptors A pKi 7.6 7.6 7.6 Guide to Pharmacology
α1D ADA1D Rat Adrenoceptors A pKd 7.27 7.83 9.21 ChEMBL
α1D ADA1D Rat Adrenoceptors A pKi 9.24 9.24 9.24 ChEMBL
α1B ADA1B Rat Adrenoceptors A pKd 9.16 9.17 9.18 ChEMBL
α1B ADA1B Human Adrenoceptors A pKi 9.16 9.6 9.87 ChEMBL
α1A ADA1A Rat Adrenoceptors A pKi 8.77 8.77 8.77 ChEMBL
α1A ADA1A Rat Adrenoceptors A pKd 7.48 7.98 8.91 ChEMBL
α1D ADA1D Human Adrenoceptors A pKi 7.5 8.56 9.77 ChEMBL
D2 DRD2 Rat Dopamine A pKi 5.08 5.08 5.08 ChEMBL
α1A ADA1A Human Adrenoceptors A pKi 7.6 7.92 8.26 ChEMBL
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pKi 5.21 5.21 5.21 ChEMBL
α1A ADA1A Bovine Adrenoceptors A pKi 8.62 8.62 8.62 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database