Benzquinamide

drug
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Also known as BenzchinamideBenzquinamidaNSC-108159NSC-169193NSC-64375P-2647PromeconQuantrilSID170465138

Summary

Benzquinamide (CHEMBL1201250) is an approved small-molecule H1-receptor antagonist targeting PTGS2 and DRD2.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Targets: 2 (PTGS2, DRD2)
  • Chemistry: 404.5 Da · C22H32N2O5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201250
NameBenzquinamide
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID2342
ChEBICHEBI:27662
Molecular formulaC22H32N2O5
Molecular weight404.5
InChIKeyJSZILQVIPPROJI-UHFFFAOYSA-N

SMILES: CCN(CC)C(=O)C1CN2CCC3=CC(=C(C=C3C2CC1OC(=O)C)OC)OC

IUPAC name: [3-(diethylcarbamoyl)-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl] acetate

Pharmacological roles (ChEBI): antiemetic, sedative, H1-receptor antagonist, muscarinic antagonist, antipsychotic agent.

Also known as: Benzchinamide, Benzquinamida, Benzquinamide, NSC-108159, NSC-169193, NSC-64375, P-2647, Promecon, Quantril, BENZQUINAMIDE, SID170465138, benzquinamide

Parent form; salt/anhydrous children: CHEMBL1200707

Patent coverage: 709 distinct patent families (3,202 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 3,139 (98%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
PTGS2COX-2Inhibition8.320%P35354
DRD2D2 receptorAgonist5.40%P14416

Broader ChEMBL bioactivity targets: 10 (assay-derived). Sample: 5-hydroxytryptamine receptor 2B, Alpha-2A adrenergic receptor, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, D(2) dopamine receptor, 5-hydroxytryptamine receptor 2A, 5-hydroxytryptamine receptor 2C, Prostaglandin G/H synthase 2, D(3) dopamine receptor, Prostaglandin G/H synthase 1.

Bioactivity

ChEMBL activities: 10 potent at pChembl ≥ 5 of 12 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
HTR2B6.5AC50320nMCHEMBL_ACT_25227441
HTR2A6.23AC50587.6nMCHEMBL_ACT_25173584
ADRA2A6.13AC50734.8nMCHEMBL_ACT_25219808
ADRA2B5.99AC501033nMCHEMBL_ACT_25143613
HTR2A5.8AC501572nMCHEMBL_ACT_25225089
ADRA2C5.77AC501700nMCHEMBL_ACT_25147786
DRD25.6AC502500nMCHEMBL_ACT_25140242
Q639215.57AC502720nMCHEMBL_ACT_25174309
ADRA2A5.52AC503030nMCHEMBL_ACT_25155916
PTGS25.02AC509629nMCHEMBL_ACT_25166107

Target pathways

Aggregated over 2 target gene(s): PTGS2, DRD2.

Top Reactome pathways

9 total, by targets touching each:

PathwayTargetsGenes
Synthesis of 15-eicosatetraenoic acid derivatives1PTGS2
Synthesis of Prostaglandins (PG) and Thromboxanes (TX)1PTGS2
Dopamine receptors1DRD2
Interleukin-10 signaling1PTGS2
Interleukin-4 and Interleukin-13 signaling1PTGS2
Biosynthesis of DHA-derived SPMs1PTGS2
Biosynthesis of EPA-derived SPMs1PTGS2
Biosynthesis of DPAn-3 SPMs1PTGS2
Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives1PTGS2

Dominant GO biological processes

GO termTargets
prostaglandin biosynthetic process1
response to oxidative stress1
embryo implantation1
regulation of blood pressure1
response to nematode1
response to selenium ion1
positive regulation of vascular endothelial growth factor production1
cyclooxygenase pathway1
lipoxygenase pathway1
positive regulation of prostaglandin biosynthetic process1
positive regulation of fever generation1
prostaglandin secretion1
regulation of cell population proliferation1
long-chain fatty acid biosynthetic process1
positive regulation of nitric oxide biosynthetic process1

Indications & clinical

Indications

0 indications (0 at ChEMBL trial phase 4).

Clinical trials

Total trials: 0.

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

452 molecules share ≥1 primary target. Top 60 by shared-target count:

MoleculeSourceStatusShared targets
DihydroergotamineChEMBL + PubChemPhase 4 (approved)DRD2, PTGS2
FIDAXOMICINChEMBL + PubChemPhase 4 (approved)DRD2, PTGS2
ACETOPHENAZINEChEMBLPhase 4 (approved)DRD2, PTGS2
AMODIAQUINEChEMBLPhase 4 (approved)DRD2, PTGS2
AMSACRINEChEMBLPhase 4 (approved)DRD2, PTGS2
APOMORPHINEChEMBLPhase 4 (approved)DRD2, PTGS2
ARFORMOTEROLChEMBLPhase 4 (approved)DRD2, PTGS2
BAZEDOXIFENEChEMBLPhase 4 (approved)DRD2, PTGS2
BEPRIDILChEMBLPhase 4 (approved)DRD2, PTGS2
CANNABIDIOLChEMBLPhase 4 (approved)DRD2, PTGS2
CLOTRIMAZOLEChEMBLPhase 4 (approved)DRD2, PTGS2
DAUNORUBICINChEMBLPhase 4 (approved)DRD2, PTGS2
DIETHYLSTILBESTROLChEMBLPhase 4 (approved)DRD2, PTGS2
DOBUTAMINEChEMBLPhase 4 (approved)DRD2, PTGS2
EPINEPHRINEChEMBLPhase 4 (approved)DRD2, PTGS2
ERGOTAMINEChEMBLPhase 4 (approved)DRD2, PTGS2
HALOPERIDOLChEMBLPhase 4 (approved)DRD2, PTGS2
INDOCYANINE GREEN ACID FORMChEMBLPhase 4 (approved)DRD2, PTGS2
LASOFOXIFENEChEMBLPhase 4 (approved)DRD2, PTGS2
LOFEPRAMINEChEMBLPhase 4 (approved)DRD2, PTGS2
MASOPROCOLChEMBLPhase 4 (approved)DRD2, PTGS2
MICONAZOLEChEMBLPhase 4 (approved)DRD2, PTGS2
NITROXOLINEChEMBLPhase 4 (approved)DRD2, PTGS2
NOREPINEPHRINEChEMBLPhase 4 (approved)DRD2, PTGS2
OLANZAPINEChEMBLPhase 4 (approved)DRD2, PTGS2
OXAPROZINChEMBLPhase 4 (approved)DRD2, PTGS2
OXYPERTINEChEMBLPhase 4 (approved)DRD2, PTGS2
PIMOZIDEChEMBLPhase 4 (approved)DRD2, PTGS2
PYRVINIUMChEMBLPhase 4 (approved)DRD2, PTGS2
RALOXIFENEChEMBLPhase 4 (approved)DRD2, PTGS2
RIFAMPINChEMBLPhase 4 (approved)DRD2, PTGS2
ROTIGOTINEChEMBLPhase 4 (approved)DRD2, PTGS2
TEGASERODChEMBLPhase 4 (approved)DRD2, PTGS2
PROCATEROLChEMBLPhase 3DRD2, PTGS2
BOPINDOLOLChEMBLPhase 2DRD2, PTGS2
AfatinibPubChemApprovedDRD2, PTGS2
ApixabanPubChemApprovedDRD2, PTGS2
BinimetinibPubChemApprovedDRD2, PTGS2
BosentanPubChemApprovedDRD2, PTGS2
chenodiolPubChemApprovedDRD2, PTGS2
FulvestrantPubChemApprovedDRD2, PTGS2
ImipenemPubChemApprovedDRD2, PTGS2
LinagliptinPubChemApprovedDRD2, PTGS2
PropoxyphenePubChemApprovedDRD2, PTGS2
PyrazinamidePubChemApprovedDRD2, PTGS2
3,3’,4’,5-TETRACHLOROSALICYLANILIDEChEMBLPhase 4 (approved)PTGS2
ABEMACICLIBChEMBLPhase 4 (approved)PTGS2
ACALABRUTINIBChEMBLPhase 4 (approved)PTGS2
ACEMETACINChEMBLPhase 4 (approved)PTGS2
ACETYLCYSTEINEChEMBLPhase 4 (approved)PTGS2
ACRIVASTINEChEMBLPhase 4 (approved)PTGS2
AMIODARONEChEMBLPhase 4 (approved)DRD2
AMISULPRIDEChEMBLPhase 4 (approved)DRD2
AMITRIPTYLINEChEMBLPhase 4 (approved)DRD2
AMLODIPINEChEMBLPhase 4 (approved)DRD2
AMOXAPINEChEMBLPhase 4 (approved)DRD2
AMPHOTERICIN BChEMBLPhase 4 (approved)PTGS2
ANISINDIONEChEMBLPhase 4 (approved)PTGS2
ARIPIPRAZOLEChEMBLPhase 4 (approved)DRD2
ARMODAFINILChEMBLPhase 4 (approved)DRD2