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Trimethoprim Bacterial chemical

Cat.No.S3129

Trimethoprim (BW 56-72, NIH 204, NSC-106568) is a bacteriostatic antibiotic mainly used in the prophylaxis and treatment of urinary tract infections.
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Quality Control

Batch: Purity: 99.96%
99.96

Solubility

In vitro
Batch:

DMSO : 58 mg/mL (199.77 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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%
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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 290.32 Formula

C14H18N4O3

Storage (From the date of receipt)
CAS No. 738-70-5 Download SDF Storage of Stock Solutions

Synonyms BW 56-72, NIH 204, NSC-106568 SMILES COC1=CC(=CC(=C1OC)OC)CC2=CN=C(N=C2N)N

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

In vitro
Trimethoprim acts by interfering with the action of bacterial dihydrofolate reductase, inhibiting synthesis of tetrahydrofolic acid. The Inhibition starves the bacteria of nucleotides necessary for DNA replication causing, in certain circumstances, cell lethality due to thymineless death.
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-03-20)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT07485010 NOT_YET_RECRUITING
Mycobacterium Abscessus Pulmonary Disease; Mycobacterium Abscessus Infection; Non-Tuberculous Mycobacterial (NTM) Infections; Non-Tuberculous Mycobacteria Pulmonary Disease
The University of Queensland
2027-04 PHASE2
NCT04851015 RECRUITING
Pneumocystis; Pneumocystis Pneumonia; Pneumocystis Jirovecii Infection; Pneumocystis Infections; Pneumocystis Carinii Infection; Pneumocystosis; Pneumonia (Etiology); Pneumocystis Carinii; Infection, Resulting From HIV Disease; Pneumocystosis Associated With AIDS
Todd C. Lee MD MPH FIDSA
2025-11-28 PHASE3
NCT07665359 NOT_YET_RECRUITING
Chronic Obstructive Pulmonary Disease (COPD)
Second Affiliated Hospital, Zhejiang University, School of Medicine
2026-07-01
NCT07106125 NOT_YET_RECRUITING
Kidney Transplant; Urinary Tract Infection(UTI); Antibiotic Prophylaxis; Remote Patient Monitoring; Feasibility Pilot Study
University of California, San Francisco
2026-11 PHASE4
NCT07619027 NOT_YET_RECRUITING
Pneumocystis Jirovecii Pneumonia; Kidney Transplantation
Anhui Provincial Hospital
2026-06 PHASE4
NCT05268120 RECRUITING
MRSA
Leiden University Medical Center
2022-07-25

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