trifluoperazine


SMILES CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(cc2)C(F)(F)F
InChIKey ZEWQUBUPAILYHI-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 0
Rotatable bonds 4
Molecular weight (Da) 407.2

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 8.22 8.22 8.22 Drug Central
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 4.92 5.47 6.02 PDSP Ki database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 8.1 8.1 8.1 Drug Central
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 6.87 7.81 8.13 PDSP Ki database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 7.9 7.9 7.9 Guide to Pharmacology
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 8.19 8.19 8.19 Drug Central
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 6.42 6.42 6.42 PDSP Ki database
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 6.4 6.4 6.4 Guide to Pharmacology
5-HT6 5HT6R Human 5-Hydroxytryptamine A pKi 8.16 8.16 8.16 Drug Central
5-HT6 5HT6R Human 5-Hydroxytryptamine A pKi 6.77 6.85 6.93 PDSP Ki database
5-HT7 5HT7R Human 5-Hydroxytryptamine A pKi 8.18 8.18 8.18 Drug Central
5-HT7 5HT7R Human 5-Hydroxytryptamine A pKi 6.54 6.54 6.54 PDSP Ki database
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 5.89 5.89 5.89 PDSP Ki database
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 5.66 5.66 5.66 PDSP Ki database
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 8.22 8.22 8.22 Drug Central
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 6.0 6.0 6.0 PDSP Ki database
α1A ADA1A Human Adrenoceptors A pKi 8.12 8.12 8.12 Drug Central
α1D ADA1D Human Adrenoceptors A pKi 7.62 7.62 7.62 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 8.21 8.21 8.21 Drug Central
α2A ADA2A Human Adrenoceptors A pKi 6.18 6.18 6.18 PDSP Ki database
α2B ADA2B Human Adrenoceptors A pKi 8.17 8.17 8.17 Drug Central
α2B ADA2B Human Adrenoceptors A pKi 6.79 6.79 6.79 PDSP Ki database
α2C ADA2C Human Adrenoceptors A pKi 8.19 8.19 8.19 Drug Central
α2C ADA2C Human Adrenoceptors A pKi 6.41 6.41 6.41 PDSP Ki database
D2 DRD2 Human Dopamine A pKi 8.05 8.05 8.05 Drug Central
D2 DRD2 Human Dopamine A pKi 8.17 8.75 9.02 PDSP Ki database
D2 DRD2 Human Dopamine A pKi 8.89 8.96 9.02 Guide to Pharmacology
D3 DRD3 Human Dopamine A pKi 8.03 8.03 8.03 Drug Central
D3 DRD3 Human Dopamine A pKi 9.02 9.22 9.35 PDSP Ki database
D4 DRD4 Human Dopamine A pKi 8.13 8.13 8.13 Drug Central
D4 DRD4 Human Dopamine A pKi 7.36 7.4 7.49 PDSP Ki database
D4 DRD4 Human Dopamine A pKi 7.36 7.36 7.36 Guide to Pharmacology
H1 HRH1 Human Histamine A pKi 8.14 8.14 8.14 Drug Central
H1 HRH1 Human Histamine A pKi 7.2 7.2 7.21 PDSP Ki database
H1 HRH1 Human Histamine A pKi 7.2 7.2 7.2 Guide to Pharmacology
5-HT6 5HT6R Rat 5-Hydroxytryptamine A pKi 7.18 7.18 7.18 PDSP Ki database
5-HT2C 5HT2C Rat 5-Hydroxytryptamine A pKi 6.42 6.71 7.0 PDSP Ki database
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pKi 8.19 8.19 8.19 Drug Central
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pKi 6.39 6.39 6.39 ChEMBL
D1 DRD1 Bovine Dopamine A pKi 6.13 6.13 6.13 PDSP Ki database
D2 DRD2 Bovine Dopamine A pKi 8.68 8.68 8.68 PDSP Ki database
H1 HRH1 Rat Histamine A pKi 6.74 6.74 6.74 PDSP Ki database
D2 DRD2 Dog Dopamine A pKi 8.92 8.92 8.92 PDSP Ki database
5-HT7 5HT7R Guinea pig 5-Hydroxytryptamine A pKi 5.0 5.42 5.84 PDSP Ki database
5-HT7 5HT7R Rat 5-Hydroxytryptamine A pKi 7.1 7.1 7.1 PDSP Ki database
D4 DRD4 Rat Dopamine A pKi 7.72 7.72 7.72 PDSP Ki database
D2 DRD2 Rat Dopamine A pKd 8.03 8.03 8.03 Drug Central
D2 DRD2 Rat Dopamine A pKi 9.7 9.71 9.72 PDSP Ki database
D2 DRD2 Rat Dopamine A pKd 9.27 9.27 9.27 ChEMBL
D2 DRD2 Rat Dopamine A pKi 8.66 8.66 8.66 ChEMBL
M3 ACM3 Rat Acetylcholine (muscarinic) A pKi 6.0 6.0 6.0 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
TSH TSHR Human Glycoprotein hormone A Potency 4.5 4.5 4.5 ChEMBL
NPS NPSR1 Human Neuropeptide S A Potency 4.6 4.7 4.9 ChEMBL
D2 DRD2 Rat Dopamine A pIC50 7.8 7.8 7.8 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 5.0 5.0 5.0 ChEMBL