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Ampicillin sodium Selection Antibiotics for Transfected Cell inhibitor

Cat.No.S3170

Ampicillin(D-(-)-α-Aminobenzylpenicillin sodium salt) is a beta-lactam antibiotic that is part of the aminopenicillin family.
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Quality Control

Batch: Purity: >97%
97

Solubility

In vitro
Batch:

DMSO : 74 mg/mL (199.25 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 74 mg/mL

Ethanol : 74 mg/mL

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Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg
g
μL

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO
%
% Tween 80
% ddH2O
% DMSO
+
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Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 371.39 Formula

C16H18N3NaO4S

Storage (From the date of receipt)
CAS No. 69-52-3 Download SDF Storage of Stock Solutions

Synonyms D-(-)-α-Aminobenzylpenicillin sodium salt SMILES CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)[O-])C.[Na+]

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
beta-lactamase
In vitro

Belonging to the penicillin group of beta-lactam antibiotics, ampicillin is able to penetrate Gram-positive and some Gram-negative bacteria. Ampicillin acts as a competitive inhibitor of the enzyme transpeptidase, which is needed by bacteria to make their cell walls. Ampicillin inhibits the third and final stage of bacterial cell wall synthesis in binary fission, which ultimately leads to cell lysis.

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2025-12-18)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT07183462 RECRUITING
Pregnancy Complications, Infectious; Premature Birth; Neonatal Diseases and Abnormalities; Antibiotic Prophylaxis; Latency Period; Prematurity
Sheba Medical Center
2025-09-10 PHASE4
NCT05977400 NOT_YET_RECRUITING
Premature Birth; Antibiotics; Neurodevelopment
Sharp HealthCare
2024-04 PHASE3
NCT06406114 RECRUITING
Drug Allergy; Cephalosporin Allergy; Drug Hypersensitivity; Antibiotic Allergy; Beta Lactam Adverse Reaction; Drug-Induced Anaphylaxis; Cephalosporin Reaction
Massachusetts General Hospital
2025-05-05 PHASE2
NCT06494072 RECRUITING
Community Acquired Pneumonia in Children
Medical College of Wisconsin
2024-08-22 PHASE4
NCT07326540 RECRUITING
Hospital Acquired Bacterial Pneumonia (HABP); Ventilator Associated Bacterial Pneumonia (VABP); Colistin Resistanrt ABC; Acinetobacter Baumannii-calcoaceticus Complex
BioVersys SAS
2026-03-27 PHASE3
NCT06423898 RECRUITING
Endocarditis, Infective
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
2024-10-09 PHASE4

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