Substance

ID:180850

Names and Identifiers
IUPAC Traditional name
trimethoprim
IUPAC name
5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine
Synonyms
2,4-二氨基-5-(3,4,5-三甲氧基苄基)嘧啶甲氧苄啶Trimethoprim
Registration numbers
Beilstein Number
CAS Number
EC Number
MDL Number
PubChem SID
Properties
Physical Property
Apperance
white powder
Solubility
DMSO: soluble
Pharmacology Properties
Gene Information
human ... DHFRP1(573971), KCNH1(3756)rat ... Dhfr(24312)
Safety Information
RTECS
UV8225000
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature
2-8°C
Product Information
Purity
≥98% (TLC)
Molecule Details
Application
Primarily used as an antibacterial agent. Dihydrofolate reductase inhibitor with selectivity for the prokaryote enzyme.
Trimethoprim is primarily used as an antibacterial agent. It has dihydrofolate reductase inhibitor activity with selectivity for the prokaryote enzyme. It is used to treat urinary tract infections, mild acute prostatitis, recurrent cystitis, asymptomatic bacteriuria during pregnancy and respiratory tract infections1.
Other Notes
Specific inhibitor of formulation. Widely used in studies on dihydrofolate reductase2,3.
Biochem/physiol Actions
The combination of trimethoprim and sulfamethoxazole interferes with the cellular metabolism of folic acid in the bacterial cell by blocking the biosynthesis of nucleotides. Trimethoprim binds to dihydrofolate reductase and inhibits the reduction of dihydrofolic acid (DHF) to tetrahydrofolic acid (THF). THF is an essential precursor in the thymidine synthesis pathway and interference with this pathway inhibits bacterial DNA synthesis1.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Molecular Spectra
No Data Available
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References
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