Ticarcillin

CHEMBL1449 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
384.4 g/mol
LogP
0.8
Phase
4

Ticarcillin is an extended-spectrum carboxypenicillin antibiotic that inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), disrupting peptidoglycan cross-linking and leading to cell lysis. It is particularly active against Pseudomonas aeruginosa and is used in combination with clavulanate (Timentin) for serious gram-negative and mixed infections including nosocomial pneumonia, urinary tract infections, and intra-abdominal infections. Its anti-pseudomonal activity addressed a major gap in penicillin coverage.

Peso Molecular

384,4000 g/mol

LogP

0,80

TPSA

178,00 Ų

Regra dos 5 de Lipinski

Aprovado

Áreas Terapêuticas

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Estrutura 2D

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SMILES

CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](C(=O)O)c3ccsc3)C(=O)N2[C@H]1C(=O)O

InChI

InChI=1S/C15H16N2O6S2/c1-15(2)9(14(22)23)17-11(19)8(12(17)25-15)16-10(18)7(13(20)21)6-3-4-24-5-6/h3-5,7-9,12H,1-2H3,(H,16,18)(H,20,21)(H,22,23)/t7-,8-,9+,12-/m1/s1

Molecular Formula

C15H16N2O6S2

HBD / HBA

3 / 8

Ligações Rotacionáveis

5

Átomos Pesados

25

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.

Perguntas frequentes

Ticarcillin is an extended-spectrum carboxypenicillin antibiotic that inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), disrupting peptidoglycan cross-linking and leading to cell lysis. It is particularly active against Pseudomonas aeruginosa and is used in combination with clavulanate (Timentin) for serious gram-negative and mixed infections including nosocomial pneumonia, urinary tract infections, and intra-abdominal infections. Its anti-pseudomonal activity addressed a major gap in penicillin coverage.

Yes, Ticarcillin 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). CHEMBL1449. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 36921. Chemical information database.

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

Aviso Médico

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.