Lindane

drug
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Also known as Benzene hexachloride gammaBenzene hexachloridegammaEsodermGameneGamma benzene hexachlorideGammahexachlorcyclohexaneGamma benzene hydrochlorideGammallinGammaxeneGexaneHexachloraneHexicideKwellLindanoLindanumLorexaneLorexane no 3NSC-755895

Summary

Lindane (CHEMBL15891) is an approved small-molecule GABA-gated chloride channel antagonist (ATC P03AB02); indicated across 2 conditions including parasitic infectious disease and lice infestation.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: P03AB02
  • Indications: 2 conditions
  • Chemistry: 290.8 Da · C6H6Cl6

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL15891
NameLindane
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID727
ChEBICHEBI:32888
ATCP03AB02
Molecular formulaC6H6Cl6
Molecular weight290.8
InChIKeyJLYXXMFPNIAWKQ-UHFFFAOYSA-N

SMILES: C1(C(C(C(C(C1Cl)Cl)Cl)Cl)Cl)Cl

IUPAC name: 1,2,3,4,5,6-hexachlorocyclohexane

Pharmacological roles (ChEBI): GABA-gated chloride channel antagonist, rodenticide, agrochemical, fungicide, antibacterial agent, pediculicide, ectoparasiticide.

Other ChEBI roles (chemical / environmental): persistent organic pollutant.

Also known as: Benzene hexachloride gamma, Benzene hexachloride, gamma, Esoderm, Gamene, Gamma benzene hexachloride, Gammahexachlorcyclohexane, Gamma benzene hydrochloride, Gammallin, Gammaxene, Gexane, Hexachlorane

Patent coverage: 36,702 distinct patent families (83,653 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 10 (assay-derived). Sample: Gamma-aminobutyric acid receptor subunit beta-3, GABA-A receptor; alpha-1/beta-3/gamma-2, GABA-A receptor; alpha-6/beta-3/gamma-2, GABA A receptor alpha-1/beta-1/gamma-2, Androgen receptor, Gamma-aminobutyric acid receptor subunit rho-1, Gamma-aminobutyric acid receptor subunit alpha-1/ beta-1, Gamma-aminobutyric acid receptor subunit alpha-6/beta-3, GABA receptor subunit, GABA-A receptor alpha-1/beta-3.

Bioactivity

ChEMBL activities: 9 potent at pChembl ≥ 5 of 10 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
GABRB39.05IC500.9nMCHEMBL_ACT_12563731
GABRB38.89IC501.3nMCHEMBL_ACT_12563728
GABRG28.31IC504.9nMCHEMBL_ACT_12563725
Q75NA57.96IC5011nMCHEMBL_ACT_12563704
GABRA17.92IC5012nMCHEMBL_ACT_12563722
GABRA17.68IC5021nMCHEMBL_ACT_12563719
GABRA17.17IC5067nMCHEMBL_ACT_12563713
GABRR17.04IC5091nMCHEMBL_ACT_12563710
GABRA16.95IC50112nMCHEMBL_ACT_12563716

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
parasitic infectious disease4MONDO:0005135EFO:0001067
lice infestation2MONDO:0003472MONDO:0003472

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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).