Hetacillin Potassium
A potassium salt form of hetacillin, a penicillin-class antibiotic prodrug that is converted to ampicillin in the body to treat bacterial infections. The potassium salt improves solubility for pharmaceutical formulations. It is used for the treatment of infections caused by susceptible gram-positive and gram-negative bacteria.
分子量
427.6000 g/mol
TPSA
118.00 Ų
作用机制
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)
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.
二维结构
Cite this structure
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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-].[K+]
InChI
InChI=1S/C19H23N3O4S.K/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);/q;+1/p-1/t11-,12-,13+,16-;/m1./s1
Molecular Formula
C19H22KN3O4S
HBD / HBA
1 / 6
可旋转键数
3
重原子数
28
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.
常见问题
A potassium salt form of hetacillin, a penicillin-class antibiotic prodrug that is converted to ampicillin in the body to treat bacterial infections. The potassium salt improves solubility for pharmaceutical formulations. It is used for the treatment of infections caused by susceptible gram-positive and gram-negative bacteria.
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 Potassium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201121. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 23678597. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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