Bioallethrin

CHEMBL1788403 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
302.4 g/mol
LogP
4.8
Phase
4

A synthetic pyrethroid insecticide used in topical formulations to treat head lice and scabies infestations. It kills parasites by disrupting their nervous system through effects on sodium channels. It is closely related to natural pyrethrins found in chrysanthemum flowers.

Molekularmasse

302,4000 g/mol

LogP

4,80

TPSA

43,40 Ų

Lipinski-Regel der Fünf

Bestanden

Wirkmechanismus

Disrupts sodium channel function in insect nerve cell membranes, causing prolonged depolarization, paralysis, and death of parasites and insects.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Disrupts sodium channel function in insect nerve cell membranes, causing prolonged depolarization, paralysis, and death of parasites and insects.

2D-Struktur

SVG PNG

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SMILES

C=CCC1=C(C)C(OC(=O)[C@@H]2[C@@H](C=C(C)C)C2(C)C)CC1=O

InChI

InChI=1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3/t14-,16?,17+/m1/s1

Molecular Formula

C19H26O3

HBD / HBA

- / 3

Rotierbare Bindungen

6

Schwere Atome

22

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Häufig gestellte Fragen

A synthetic pyrethroid insecticide used in topical formulations to treat head lice and scabies infestations. It kills parasites by disrupting their nervous system through effects on sodium channels. It is closely related to natural pyrethrins found in chrysanthemum flowers.

Disrupts sodium channel function in insect nerve cell membranes, causing prolonged depolarization, paralysis, and death of parasites and insects.

Yes, Bioallethrin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1788403. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 15558638. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Medizinischer Haftungsausschluss

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.