Hetacillin

CHEMBL1201116 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
389.5 g/mol
LogP
-0.6
Phase
4

A penicillin-class antibiotic that is a prodrug of ampicillin, rapidly converted to ampicillin in the body after absorption to exert its antibacterial effects. It was designed to improve oral bioavailability compared to early ampicillin formulations. Its spectrum of activity and uses are equivalent to those of ampicillin.

Molekularmasse

389,5000 g/mol

LogP

-0,60

TPSA

115,00 Ų

Lipinski-Regel der Fünf

Bestanden

Wirkmechanismus

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

2D-Struktur

SVG PNG

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SMILES

CC1(C)S[C@@H]2[C@H](N3C(=O)[C@@H](c4ccccc4)NC3(C)C)C(=O)N2[C@H]1C(=O)O

InChI

InChI=1S/C19H23N3O4S/c1-18(2)13(17(25)26)21-15(24)12(16(21)27-18)22-14(23)11(20-19(22,3)4)10-8-6-5-7-9-10/h5-9,11-13,16,20H,1-4H3,(H,25,26)/t11-,12-,13+,16-/m1/s1

Molecular Formula

C19H23N3O4S

HBD / HBA

2 / 6

Rotierbare Bindungen

3

Schwere Atome

27

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 penicillin-class antibiotic that is a prodrug of ampicillin, rapidly converted to ampicillin in the body after absorption to exert its antibacterial effects. It was designed to improve oral bioavailability compared to early ampicillin formulations. Its spectrum of activity and uses are equivalent to those of ampicillin.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Hetacillin 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). CHEMBL1201116. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 443387. 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.