| Size | Price | |
|---|---|---|
| 500mg | ||
| 1g | ||
| Other Sizes |
| ln Vitro |
SMO-IN-6 (compound 16) (72 hours) effectively inhibited the proliferation of A431 skin squamous cell carcinoma cells, with a GI50 of 1.4 μM and a therapeutic index of 31 relative to non-tumor HaCaT skin cells [1]. SMO-IN-6 (1-4 μM; 14 days) inhibited long-term colony formation of A431 skin squamous cell carcinoma cells in a dose-dependent manner, with an inhibition rate of over 95% at a concentration of 4 μM [1]. SMO-IN-6 (1 μM) effectively downregulated the expression of Hedgehog/GLI pathway target genes Gli1, Gli2, Ptch1 and HHip in A431 skin squamous cell carcinoma cells [1]. SMO-IN-6 (1-4 μM; 16 hours) induced apoptosis in A431 skin squamous cell carcinoma cells in a dose-dependent manner, with an apoptosis rate of 93% at a concentration of 4 μM [1].
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|---|---|
| ln Vivo |
SMO-IN-6 (compound 16) (10-25 mg/kg; intraperitoneal injection; 2-on-1-off dosing regimen; 14 days) dose-dependently inhibited the growth of squamous cell carcinoma tumors of the skin in BALB/c nude mice [1].
|
| Animal Protocol |
Animal/Disease Models:BALB/c nude mice (female, 6-8 weeks old, 18-20 g, subcutaneously injected with A431 cells) [1]
Doses: 10 mg/kg; 25 mg/kg Route of Administration: Intraperitoneal injection; 2-day dosing and 1-day discontinuation regimen; 14 days Experimental Results: Tumor growth inhibition rate (TGI) reached 30%. 56%. Induced approximately 40% of TUNEL-positive apoptotic cells. Significantly downregulated the expression levels of GLI1, Ki67, and SOX2 in tumor tissues. Significantly upregulated the expression level of cleaved-caspase 3 in tumor tissues. No significant weight loss, abnormal morphology of major organs, or hematologic toxicity was observed. |
| References |
| Molecular Formula |
C23H26CL2N2O3
|
|---|---|
| Molecular Weight |
449.37
|
| Appearance |
Typically exists as solids at room temperature
|
| SMILES |
C[C@]1(O[C@H](COC2=CC=C(N3CC4CCC(N4)C3)C=C2)CO1)C5=CC=C(Cl)C=C5Cl
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| HS Tariff Code |
2934.99.9001
|
| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
|
| Solubility (In Vitro) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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|---|---|
| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400 (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 2.2253 mL | 11.1267 mL | 22.2534 mL | |
| 5 mM | 0.4451 mL | 2.2253 mL | 4.4507 mL | |
| 10 mM | 0.2225 mL | 1.1127 mL | 2.2253 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution 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 stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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