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IMMH001

(Synonyms: SYL930, IMMH 001) Copy Product Info
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Synonyms: SYL930, IMMH 001

Catalog No. T61621 Copy Product Info
Purity: 99.67%
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IMMH001, also known as SYL930, is an orally active compound that functions as a highly selective agonist of sphingosine-1-phosphate receptor 1 (S1P1). IMMH001 effectively reduces the levels of multiple chemokines and proinflammatory cytokines, including IL-1β, IL-5, IL-18, IP10, CCL3, and CCL5. IMMH001 is applicable to investigations involving rheumatoid arthritis (RA), immune cell trafficking, inflammatory signaling cascades, and sphingosine-1-phosphate receptor-mediated immunoregulation.
IMMH001
Cas No. 1418093-75-0
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$117-In Stock
5 mg$289-In Stock
10 mg$463-In Stock
25 mg$928-In Stock
1 mL x 10 mM (in DMSO)$318-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.67%
Appearance:Solid
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Product Introduction

Bioactivity
Description
IMMH001, also known as SYL930, is an orally active compound that functions as a highly selective agonist of sphingosine-1-phosphate receptor 1 (S1P1). IMMH001 effectively reduces the levels of multiple chemokines and proinflammatory cytokines, including IL-1β, IL-5, IL-18, IP10, CCL3, and CCL5. IMMH001 is applicable to investigations involving rheumatoid arthritis (RA), immune cell trafficking, inflammatory signaling cascades, and sphingosine-1-phosphate receptor-mediated immunoregulation.
In vivo
IMMH001 is metabolized into its active monophosphate ester form, (S)-IMMH001-P, by the action of sphingosine kinase 1 (SphK1) and sphingosine kinase 2 (SphK2) in vivo [1]. IMMH001 effectively diminishes disease manifestations mediated by both Th1 (IL-1β, IL-18, and IP10) and Th2 (IL-5) cells in inflamed joints [2].
IMMH001 (0.3-2.4 mg/kg, Orally; twice a week, for 28 days, AA rats; for 30 days, CIA rats) significantly alleviates joint damage in these models [2].
SynonymsSYL930, IMMH 001
Chemical Properties
Molecular Weight380.48
FormulaC23H28N2O3
Cas No.1418093-75-0
SmilesOCC(N)(CO)CCC=1C=CC(=CC1)C=2C=CC(=CC2)C=3N=C(OC3)CCC
Storage & Solubility Information
StorageKeep away from direct sunlight,Keep away from moisture,Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (210.26 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6283 mL13.1413 mL26.2826 mL131.4130 mL
5 mM0.5257 mL2.6283 mL5.2565 mL26.2826 mL
10 mM0.2628 mL1.3141 mL2.6283 mL13.1413 mL
20 mM0.1314 mL0.6571 mL1.3141 mL6.5706 mL
50 mM0.0526 mL0.2628 mL0.5257 mL2.6283 mL
100 mM0.0263 mL0.1314 mL0.2628 mL1.3141 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 µL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 µL Tween 80 and mix well until fully clarified.

3) Add 450 µL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
µL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Related Tags: IMMH001 chemical structure | IMMH001 in vivo | IMMH001 formula | IMMH001 molecular weight