SQDG [123036-44-2]
Referência HY-143692-1mg
Tamanho : 1mg
Marca : MedChemExpress
| Description |
SQDG inhibits topoisomerase I and P-selectin receptor, exhibits anti-inflammatory, antiviral and antitumor activities. SQDG is a glycolipid that possesses sugar moieties in their head groups. SQDG is a membrane lipid that can be used to investigate the effects of structural lipid in LNP formulations[1][2][3]. |
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| In Vitro |
SQDG is an acidic lipid that can be found in the thylakoid membrane of photosynthetic organisms such as plants and cyanobacteria. SQDG is the composition of the thylakoid membrane, provides a stable environment for membrane proteins and maintains the integrity of the membrane[2]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Cell Cycle Analysis[4]
Apoptosis Analysis[4]
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| In Vivo |
SQDG (2 mg/kg, ip, two doses in a week) exhibits antitumor efficacy in MOLT-4 xenograft mouse models[4]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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| Masse moléculaire |
817.12 |
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| Formule |
C43H76O12S |
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| CAS No. | |||||||||||||||||
| Appearance |
Solid |
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| Color |
White to light yellow |
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| SMILES |
CC/C=C\C/C=C\C/C=C\CCCCCCCC(OC[C@@H](OC(CCCCCCCCCCCCCCC)=O)CO[C@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CS(=O)(O)=O)=O |
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| Livraison | Room temperature in continental US; may vary elsewhere. |
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| Stockage |
-20°C, protect from light, stored under nitrogen *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen) |
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| Solvant et solubilité |
In Vitro:
DMSO : 1 mg/mL (1.22 mM; Need ultrasonic and warming; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) Preparing
Stock Solutions
View the Complete Stock Solution Preparation Table
*
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol) Concentration (start) × Volume (start) = Concentration (final) × Volume (final) This equation is commonly abbreviated as: C1V1 = C2V2 In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
Dosage mg/kgAnimal weight Dosing volume Number of animals Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration:
mg/mL
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| Pureté et documentation |
Purity: 99.0% |
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| Références |
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