research use only
Cat.No.S1725
| Related Targets | Integrase Bacterial Antibiotics Anti-infection Antiviral COVID-19 Parasite Reverse Transcriptase HIV HCV Protease |
|---|---|
| Other Fungal Inhibitors | Cycloheximide Tolnaftate Manogepix (E1210) Amorolfine HCl Isavuconazole Juglone Bifonazole Thimerosal Pseudolaric Acid B Butylparaben |
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In vitro |
DMSO
: 58 mg/mL
(199.01 mM)
Ethanol : 58 mg/mL Water : Insoluble |
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In vivo |
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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.
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| Molecular Weight | 291.43 | Formula | C21H25N |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 91161-71-6 | Download SDF | Storage of Stock Solutions |
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| 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
| 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 |
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(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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