Molecule Details
InChIKeyZEWQUBUPAILYHI-UHFFFAOYSA-N
Compound NameTrifluoperazine
Canonical SMILESCN1CCN(CCCN2c3ccccc3Sc3ccc(C(F)(F)F)cc32)CC1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)21
Pfam Stratification Cross-Family
Avg pChEMBL7.05
SourceBindingDB;ChEMBL
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB00831
Drug NameTrifluoperazine
CAS Number117-89-5
Groups approved investigational
ATC Codes N05AB06
DescriptionA phenothiazine with actions similar to chlorpromazine. It is used as an antipsychotic and an antiemetic.

Categories: Adrenergic Antagonists Adrenergic alpha-1 Receptor Antagonists Adrenergic alpha-Antagonists Agents that produce hypertension Antiemetics Antipsychotic Agents Antipsychotic Agents (First Generation [Typical]) Autonomic Agents Central Nervous System Agents Central Nervous System Depressants Cytochrome P-450 CYP1A2 Substrates Cytochrome P-450 Substrates Dopamine Agents Dopamine Antagonists Dopamine D2 Receptor Antagonists Drugs causing inadvertant photosensitivity Gastrointestinal Agents Heterocyclic Compounds, Fused-Ring Nervous System Neurotoxic agents Neurotransmitter Agents P-glycoprotein inhibitors P-glycoprotein substrates Peripheral Nervous System Agents Phenothiazines Phenothiazines With Piperazine Structure Photosensitizing Agents Psycholeptics Psychotropic Drugs Sulfur Compounds Tranquilizing Agents UGT1A4 substrates
Cross-references: BindingDB: 79181 ChEBI: 45951 CHEMBL422 ChemSpider: 5365 Drugs Product Database (DPD): 7996 Guide to Pharmacology: 214 IUPHAR: 214 C07168 D08636 PDB: TFP PharmGKB: PA451771 PubChem:5566 PubChem:46507961 RxCUI: 10800 Therapeutic Targets Database: DAP000034 Wikipedia: Trifluoperazine ZINC: ZINC000019418959
Target Activities (21)
Target Gene Organism Category Pfam pChEMBL Type Source
P35462 DRD3 Homo sapiens Human PF00001 9.3 Ki BindingDB
P14416 DRD2 Homo sapiens Human PF00001 8.9 Ki BindingDB
Q9BY08 EBPL Homo sapiens Human PF05241 8.4 Ki ChEMBL;BindingDB
Q15125 EBP Homo sapiens Human PF05241 8.1 Ki ChEMBL;BindingDB
Q99720 SIGMAR1 Homo sapiens Human PF04622 7.8 Ki ChEMBL;BindingDB
P35348 ADRA1A Homo sapiens Human PF00001 7.6 Ki BindingDB
P28223 HTR2A Homo sapiens Human PF00001 7.4 Ki BindingDB
P21917 DRD4 Homo sapiens Human PF00001 7.4 Ki BindingDB
P35367 HRH1 Homo sapiens Human PF00001 7.2 Ki BindingDB
P50406 HTR6 Homo sapiens Human PF00001 6.8 Ki BindingDB
P18089 ADRA2B Homo sapiens Human PF00001 6.8 Ki BindingDB
P34969 HTR7 Homo sapiens Human PF00001 6.5 Ki BindingDB
P28335 HTR2C Homo sapiens Human PF00001 6.4 Ki BindingDB
P18825 ADRA2C Homo sapiens Human PF00001 6.4 Ki BindingDB
P08172 CHRM2 Homo sapiens Human PF00001 6.2 Ki BindingDB
P08913 ADRA2A Homo sapiens Human PF00001 6.2 Ki BindingDB
P08908 HTR1A Homo sapiens Human PF00001 6.0 Ki BindingDB
P08922 ROS1 Homo sapiens Human PF00041 PF07714 6.0 IC50 BindingDB
P0DP23 CALM1 Homo sapiens Human PF13499 6.0 Kd ChEMBL;BindingDB
P32352 ERG2 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) Pathogen PF04622 6.3 Ki ChEMBL;BindingDB
A3EZJ3 NS3 Hepacivirus hominis Pathogen PF07652 PF22027 PF02907 6.2 IC50 ChEMBL
DrugBank Target Actions (12)
Target Gene Target Name Action Type
P47989 XDH Xanthine dehydrogenase/oxidase modulator enzymes
P05177 CYP1A2 Cytochrome P450 1A2 substrate enzymes
P22310 P22310 UDP-glucuronosyltransferase 1A4 substrate enzymes
P63316 P63316 Troponin C, slow skeletal and cardiac muscles allosteric modulator targets
P14416 DRD2 D(2) dopamine receptor antagonist targets
P35348 ADRA1A Alpha-1A adrenergic receptor antagonist targets
Q9NYX4 Q9NYX4 Neuron-specific vesicular protein calcyon antagonist targets
P0DP23 CALM1 Calmodulin-1 inhibitor targets
P0DP24 P0DP24 Calmodulin-2 inhibitor targets
P0DP25 P0DP25 Calmodulin-3 inhibitor targets
P26447 P26447 Protein S100-A4 inhibitor targets
P08183 ABCB1 ATP-dependent translocase ABCB1 inhibitor transporters