Molecule Details
InChIKeyPLDUPXSUYLZYBN-UHFFFAOYSA-N
Compound NameFluphenazine
Canonical SMILESOCCN1CCN(CCCN2c3ccccc3Sc3ccc(C(F)(F)F)cc32)CC1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)22
Pfam Stratification Cross-Family
Avg pChEMBL7.39
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB00623
Drug NameFluphenazine
CAS Number69-23-8
Groups approved
ATC Codes N05AB02
DescriptionA phenothiazine used in the treatment of psychoses. Its properties and uses are generally similar to those of chlorpromazine.

Categories: Agents that reduce seizure threshold Antidepressive Agents Antipsychotic Agents Antipsychotic Agents (First Generation [Typical]) Central Nervous System Agents Central Nervous System Depressants Cytochrome P-450 CYP2D6 Inhibitors Cytochrome P-450 CYP2D6 Inhibitors (weak) Cytochrome P-450 CYP2E1 Inhibitors Cytochrome P-450 CYP2E1 Inhibitors (weak) Cytochrome P-450 Enzyme Inhibitors Delayed-Action Preparations Dopamine Agents Dopamine Antagonists Dopamine D2 Receptor Antagonists Drugs causing inadvertant photosensitivity Heterocyclic Compounds, Fused-Ring Nervous System Neurotoxic agents Neurotransmitter Agents P-glycoprotein inhibitors Phenothiazines Phenothiazines With Piperazine Structure Photosensitizing Agents Psycholeptics Psychotropic Drugs Serotonin 5-HT2 Receptor Antagonists Serotonin 5-HT2A Receptor Antagonists Serotonin 5-HT2C Receptor Antagonists Serotonin Agents Serotonin Receptor Antagonists Sulfur Compounds Tranquilizing Agents
Cross-references: BindingDB: 78433 ChEBI: 5123 CHEMBL726 ChemSpider: 3255 Drugs Product Database (DPD): 8007 Guide to Pharmacology: 204 IUPHAR: 204 C07010 D07977 PharmGKB: PA449676 PubChem:3372 PubChem:46506645 RxCUI: 4496 Therapeutic Targets Database: DCL000806 Wikipedia: Fluphenazine ZINC: ZINC000019203912
Target Activities (22)
Target Gene Organism Category Pfam pChEMBL Type Source
P14416 DRD2 Homo sapiens Human PF00001 9.1 Ki ChEMBL;BindingDB
P35462 DRD3 Homo sapiens Human PF00001 8.8 Ki ChEMBL;BindingDB
P35348 ADRA1A Homo sapiens Human PF00001 8.1 Ki ChEMBL;BindingDB
P34969 HTR7 Homo sapiens Human PF00001 8.1 Ki ChEMBL;BindingDB
P28223 HTR2A Homo sapiens Human PF00001 7.9 Ki ChEMBL;BindingDB
Q99720 SIGMAR1 Homo sapiens Human PF04622 7.9 IC50 ChEMBL
P21918 DRD5 Homo sapiens Human PF00001 7.7 Ki ChEMBL;BindingDB
P35367 HRH1 Homo sapiens Human PF00001 7.7 Ki ChEMBL;BindingDB
P21728 DRD1 Homo sapiens Human PF00001 7.6 Ki ChEMBL;BindingDB
P25100 ADRA1D Homo sapiens Human PF00001 7.6 IC50 ChEMBL
P18825 ADRA2C Homo sapiens Human PF00001 7.5 Ki ChEMBL;BindingDB
P41595 HTR2B Homo sapiens Human PF00001 7.5 IC50 ChEMBL
P50406 HTR6 Homo sapiens Human PF00001 7.4 Ki ChEMBL;BindingDB
P18089 ADRA2B Homo sapiens Human PF00001 7.3 Ki ChEMBL;BindingDB
P21917 DRD4 Homo sapiens Human PF00001 7.3 Ki ChEMBL;BindingDB
P28335 HTR2C Homo sapiens Human PF00001 6.9 Ki ChEMBL;BindingDB
P08908 HTR1A Homo sapiens Human PF00001 6.8 Ki ChEMBL;BindingDB
P08913 ADRA2A Homo sapiens Human PF00001 6.5 Ki ChEMBL;BindingDB
P08173 CHRM4 Homo sapiens Human PF00001 6.3 Ki ChEMBL
P11229 CHRM1 Homo sapiens Human PF00001 6.2 Ki ChEMBL
P31645 SLC6A4 Homo sapiens Human PF03491 PF00209 6.1 Ki ChEMBL
P20309 CHRM3 Homo sapiens Human PF00001 6.0 Ki ChEMBL
DrugBank Target Actions (10)
Target Gene Target Name Action Type
P05181 CYP2E1 Cytochrome P450 2E1 inhibitor enzymes
P10635 CYP2D6 Cytochrome P450 2D6 inhibitor enzymes
P10275 AR Androgen receptor antagonist targets
P14416 DRD2 D(2) dopamine receptor antagonist targets
P21728 DRD1 D(1A) dopamine receptor antagonist targets
P28223 HTR2A 5-hydroxytryptamine receptor 2A antagonist targets
P28335 HTR2C 5-hydroxytryptamine receptor 2C antagonist targets
P0DP23 CALM1 Calmodulin inhibitor targets
P28222 HTR1B 5-hydroxytryptamine receptor 1B modulator targets
P08183 ABCB1 ATP-dependent translocase ABCB1 inhibitor transporters