| Size | Price | |
|---|---|---|
| 500mg | ||
| 1g | ||
| Other Sizes |
| Targets |
RXRα (Retinoid X receptor alpha)[1]
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|---|---|
| ln Vitro |
XS-060 is an antimitotic drug with good anti-tumor activity that targets the coactivator binding region of RXRα' and inhibits the pRXRα-PLK1 connection [1]. Anti-proliferative effect against MDA-MB 231 cancer cells is demonstrated by XS-060, with an IC50 of 6.880 ± 0.059 μM[1].
|
| ln Vivo |
Oral delivery of XS-060 (25 mg/kg, IP or PO, once) results in inadequate absorption compared to intraperitoneal injection[1].
|
| Cell Assay |
Cell Proliferation Assay[1]
Cell Types: MDA-MB 231, A549, and HepG2 Tested Concentrations: 5 μM Incubation Duration: Experimental Results: demonstrated anti-proliferative activity at 5 μM against cancer cells (MDA-MB 231, A549, and HepG2), with cell viability rate (%) of 51.93 ± 4.32, 82.65 ± 2.84, and 48.65 ± 6.45, respectively. |
| Animal Protocol |
Animal/Disease Models: SD (Sprague-Dawley) rats (10-14 weeks, 200-220g)[1]
Doses: 25 mg/kg Route of Administration: Oral absorption (po) and intraperitoneal (ip) injection (ip), once, (pharmacokinetic/PK Analysis) Experimental Results: The oral absorption of XS-060 is very poor, while intraperitoneal (ip) injection displayed good absorption[1]. pharmacokinetic/PK Parameters of XS-060 in SD (Sprague-Dawley) rats[1]. XS060 25 mg/kg (ip) Tmax (h) 2.67 ± 1.12 Cmax (μg/L) 1061.50 ± 399.20 AUC0-∞ (μg⋅h/L) 7040.30 ± 1593.52 T1/2 (h) 2.13 ± 0.05 CLz/F (L/(h⋅kg)) 3.67 ± 0.81 Vd, z/F (L/kg) 11.31 ± 2.71 |
| References |
|
| CAS # |
2787626-06-4
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|---|---|
| Appearance |
Off-white to yellow solid powder
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| HS Tariff Code |
2934.99.9001
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| 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.) |
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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