SQDG [123036-44-2]

Référence HY-143692-1mg

Conditionnement : 1mg

Marque : 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].

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].
SQDG binds to four sites of photosystem II (PSII) and affects PSII activity. SQDG regulates the efficiency of photosynthesis. SQDG loss leads to growth inhibition in some cyanobacteria[2].
SQDG inhibits herpes simplex virus type 2 (HSV-1), HSV-2 (IC50=15.6 μg/mL) and Coxsackie virus B3 (Cox B3)[3].
SQDG (0-25 μM, 72 h) exhibits cytotoxicity in acute lymphoblastic leukemia (ALL) cells, IC50s for MOLT-4, MOLT-3 and Reh are 15.32 μM, 22.52 μM and 19.63 μM[4].
SQDG (0-25 μM, 24-48 h) arrests the cell cycle at S phase, and induces apoptosis in MOLT-4 through p53-dependent pathway[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cycle Analysis[4]

Cell Line: MOLT-4
Concentration: 0-25 μM
Incubation Time: 24 h
Result: Arrested the cell cycle at S phase.

Apoptosis Analysis[4]

Cell Line: MOLT-4
Concentration: 0-25 μM
Incubation Time: 48 h
Result: Induced apoptosis.
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.

Animal Model: MOLT-4 xenograft mouse models[4]
Dosage: 2 mg/kg
Administration: ip, two doses in a week
Result: Inhibited the tumor growth.
Masse moléculaire

817.12

Formule

C43H76O12S

CAS No.
Appearance

Solid

Color

White to light yellow

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

Livraison

Room temperature in continental US; may vary elsewhere.

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)

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
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.2238 mL 6.1191 mL 12.2381 mL
5 mM --- --- ---
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.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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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
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Pureté et documentation
Références