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Lalistat 2 1234569-09-5

Lalistat 2 1234569-09-5

CAS No.: 1234569-09-5

Lalistat 2 is a specific inhibitor of lysosomal acid lipase (LAL) and has no effect on other forms of lipase.
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This product is for research use only, not for human use. We do not sell to patients.

Lalistat 2 is a specific inhibitor of lysosomal acid lipase (LAL) and has no effect on other forms of lipase.

Physicochemical Properties


Molecular Formula C13H20N4O2S
Molecular Weight 296.39
Exact Mass 296.13
CAS # 1234569-09-5
PubChem CID 46867138
Appearance White to off-white solid powder
Density 1.3±0.1 g/cm3
Boiling Point 438.5±45.0 °C at 760 mmHg
Flash Point 219.0±28.7 °C
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.586
LogP 3.29
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 3
Heavy Atom Count 20
Complexity 332
Defined Atom Stereocenter Count 0
InChi Key PNYYVHOTXOEBEV-UHFFFAOYSA-N
InChi Code

InChI=1S/C13H20N4O2S/c18-13(17-9-5-2-6-10-17)19-12-11(14-20-15-12)16-7-3-1-4-8-16/h1-10H2
Chemical Name

(4-piperidin-1-yl-1,2,5-thiadiazol-3-yl) piperidine-1-carboxylate
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)

Biological Activity


References [1]. Hamilton J, et al. A new method for the measurement of lysosomal acid lipase in dried blood spots using the inhibitor Lalistat 2. Clin Chim Acta. 2012;413(15-16):1207-1210.
[2]. Lukacs Z, et al. Best practice in the measurement and interpretation of lysosomal acid lipase in dried blood spots using the inhibitor Lalistat 2. Clin Chim Acta. 2017;471:201-205.

Solubility Data


Solubility (In Vitro) DMSO: ≥ 100 mg/mL (337.39 mM)
Solubility (In Vivo) Solubility in Formulation 1: ≥ 2.5 mg/mL (8.43 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

Solubility in Formulation 2: ≥ 2.5 mg/mL (8.43 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

Solubility in Formulation 3: ≥ 2.5 mg/mL (8.43 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 3.3739 mL 16.8697 mL 33.7393 mL
5 mM 0.6748 mL 3.3739 mL 6.7479 mL
10 mM 0.3374 mL 1.6870 mL 3.3739 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.