Echothiophate

CHEMBL1201341 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
256.3 g/mol
LogP
1.0
Phase
4

An organophosphate cholinesterase inhibitor used as an eye drop to treat glaucoma and certain types of strabismus (crossed eyes). It reduces intraocular pressure by promoting the drainage of fluid from the eye.

Khối lượng phân tử

256,3300 g/mol

LogP

1,00

TPSA

60,80 Ų

Lipinski RO5

Đạt

Cơ chế tác dụng

Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.

Cấu trúc 2D

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SMILES

CCOP(=O)(OCC)SCC[N+](C)(C)C

InChI

InChI=1S/C9H23NO3PS/c1-6-12-14(11,13-7-2)15-9-8-10(3,4)5/h6-9H2,1-5H3/q+1

Molecular Formula

C9H23NO3PS+

HBD / HBA

- / 4

Liên kết có thể quay

8

Nguyên tử nặng

15

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.

Câu hỏi thường gặp

An organophosphate cholinesterase inhibitor used as an eye drop to treat glaucoma and certain types of strabismus (crossed eyes). It reduces intraocular pressure by promoting the drainage of fluid from the eye.

Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.

Yes, Echothiophate 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). CHEMBL1201341. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 10548. Chemical information database.

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

Tuyên bố miễn trách y tế

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.