Pyridostigmine Bromide

CHEMBL812 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
261.1 g/mol
LogP
Phase
4

Pyridostigmine bromide is the bromide salt form of pyridostigmine, a reversible cholinesterase inhibitor used for the symptomatic treatment of myasthenia gravis and as a prophylactic agent against organophosphate nerve agent poisoning. See pyridostigmine for complete pharmacological details.

Masse moléculaire

261,1200 g/mol

TPSA

33,40 Ų

Aires thérapeutiques

Mécanisme d'action

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)

Mécanisme

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

Structure 2D

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SMILES

CN(C)C(=O)Oc1ccc[n+](C)c1.[Br-]

InChI

InChI=1S/C9H13N2O2.BrH/c1-10(2)9(12)13-8-5-4-6-11(3)7-8;/h4-7H,1-3H3;1H/q+1;/p-1

Molecular Formula

C9H13BrN2O2

HBD / HBA

- / 3

Liaisons Rotatives

2

Atomes Lourds

14

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.

Foire aux questions

Pyridostigmine bromide is the bromide salt form of pyridostigmine, a reversible cholinesterase inhibitor used for the symptomatic treatment of myasthenia gravis and as a prophylactic agent against organophosphate nerve agent poisoning. See pyridostigmine for complete pharmacological details.

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

Yes, Pyridostigmine Bromide 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). CHEMBL812. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 7550. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Avertissement médical

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.