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Terbinafine Fungal inhibitor

Cat.No.S1725

Terbinafine (SF 86-327,TDT 067) is used to treat infections caused by a fungus. It works by killing the fungus or preventing its growth.
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Quality Control

Batch: Purity: 99.96%
99.96

Solubility

In vitro
Batch:

DMSO : 58 mg/mL (199.01 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 58 mg/mL

Water : Insoluble

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Mass Concentration Volume Molecular Weight
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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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 291.43 Formula

C21H25N

Storage (From the date of receipt)
CAS No. 91161-71-6 Download SDF Storage of Stock Solutions

Synonyms SF 86-327,TDT 067 SMILES CC(C)(C)C#CC=CCN(C)CC1=CC=CC2=CC=CC=C21

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
squalene epoxidase
In vitro

Terbinafine (50 μM to 100 μM) inhibits only marginally the metabolism of ethoxycoumarin (CYP1A2), HLS 831(CYP2C9), or ethynylestradiol, CsA, and cortisol. This compound proves to be a potent inhibitor of the CYP2D6-mediated dextromethorphan O-demethylation and bufuralol 1-hydroxylation with IC50values of 0.2 μM and 0.25 μM, respectively. It is highly activ Aspergillus isolates (minimum inhibitory concentration [MIC] 0.01 to 2 mg/mL) with a primary fungicidal action (minimum fungicidal concentration [MFC] 0.02 to 4 mg/mL). This chemical inhibits dextromethorphan O-demethylation with an apparent Ki ranging from 28 to 44 nM in human hepatic microsomes and averaging 22.4 nM for the heterologously expressed enzymes. It shows a very strong activity in vitro against Penicillium spp., Paecilomyces spp., Trichoderma spp., Acremonium spp. and Arthrographis spp. with GMs <1 mg/L. This compound decreases the levels of phosphorylated extracellular signal-regulated kinase (ERK). It might cause a decrease of MEK, which in turn up-regulates p53 through the inhibition of ERK phosphorylation, and finally causes an increase of p21expression and cell-cycle arrest.

References
  • [4] https://pubmed.ncbi.nlm.nih.gov/15102749/
  • [5] https://pubmed.ncbi.nlm.nih.gov/18272192/

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-07-31)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT07738328 NOT_YET_RECRUITING
Acute Kidney Injury; Cardiac Surgical Procedures
Guangdong Provincial People's Hospital
2026-09-01 PHASE2
NCT07738328 NOT_YET_RECRUITING
Acute Kidney Injury; Cardiac Surgical Procedures
Guangdong Provincial People's Hospital
2026-09-01 PHASE2
NCT07365423 RECRUITING
Recurrent Prostate Cancer
Swiss Cancer Institute
2026-04-24 PHASE2
NCT07365423 RECRUITING
Recurrent Prostate Cancer
Swiss Cancer Institute
2026-04-24 PHASE2
NCT07382427 NOT_YET_RECRUITING
Onychomycosis of Toenail
Onyx Axiom
2026-03 PHASE2
NCT07382427 NOT_YET_RECRUITING
Onychomycosis of Toenail
Onyx Axiom
2026-03 PHASE2

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