KETOCONAZOLE


SMILES CC(=O)N1CCN(c2ccc(OCC3COC(Cn4ccnc4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1
InChIKey XMAYWYJOQHXEEK-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 7
Hydrogen bond donors 0
Rotatable bonds 7
Molecular weight (Da) 530.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections


Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
GnRH1 GNRHR Rat Gonadotrophin-releasing hormone A pKd 6.09 8.39 9.66 ChEMBL
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pKi 5.21 5.21 5.21 ChEMBL
α1B ADA1B Rat Adrenoceptors A pKi 4.9 4.9 4.9 ChEMBL
α2B ADA2B Human Adrenoceptors A pKi 5.08 5.08 5.08 ChEMBL
NK2 NK2R Human Tachykinin A pKi 5.24 5.24 5.24 ChEMBL
α1A ADA1A Rat Adrenoceptors A pKi 4.84 4.84 4.84 ChEMBL
H2 HRH2 Human Histamine A pKi 4.67 4.67 4.67 ChEMBL
α2A ADA2A Human Adrenoceptors A pKi 5.13 5.13 5.13 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 5.03 5.03 5.03 ChEMBL
δ OPRD Human Opioid A pKi 5.35 5.35 5.35 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 8.3 8.3 8.3 Drug Central
α1D ADA1D Human Adrenoceptors A pKi 8.32 8.32 8.32 Drug Central
α2A ADA2A Human Adrenoceptors A pKi 8.29 8.29 8.29 Drug Central
α2B ADA2B Human Adrenoceptors A pKi 8.29 8.29 8.29 Drug Central
H2 HRH2 Human Histamine A pKi 8.33 8.33 8.33 Drug Central
δ OPRD Human Opioid A pKi 8.27 8.27 8.27 Drug Central
NK2 NK2R Human Tachykinin A pKi 8.28 8.28 8.28 Drug Central
α1B ADA1B Rat Adrenoceptors A pKi 8.31 8.31 8.31 Drug Central
GnRH1 GNRHR Rat Gonadotrophin-releasing hormone A pKd 8.02 8.02 8.02 Drug Central
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pKi 8.28 8.28 8.28 Drug Central
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
GnRH1 GNRHR Rat Gonadotrophin-releasing hormone A pIC50 5.7 5.7 5.7 ChEMBL
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pIC50 4.87 4.87 4.87 ChEMBL
α1B ADA1B Rat Adrenoceptors A pIC50 4.64 4.64 4.64 ChEMBL
α2B ADA2B Human Adrenoceptors A pIC50 4.74 4.74 4.74 ChEMBL
NK2 NK2R Human Tachykinin A pIC50 4.76 4.76 4.76 ChEMBL
α1A ADA1A Rat Adrenoceptors A pIC50 4.45 4.45 4.45 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.9 4.97 5.05 ChEMBL
H2 HRH2 Human Histamine A pIC50 4.66 4.66 4.66 ChEMBL
α2A ADA2A Human Adrenoceptors A pIC50 4.7 4.7 4.7 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pIC50 4.58 4.58 4.58 ChEMBL
δ OPRD Human Opioid A pIC50 4.89 4.89 4.89 ChEMBL
NPS NPSR1 Human Neuropeptide S A Potency 4.9 4.9 4.9 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.4 4.58 5.1 ChEMBL
α1A ADA1A Rat Adrenoceptors A pIC50 8.35 8.35 8.35 Drug Central