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Results for "

Sphingosine alkyne

" in MedChemExpress (MCE) Product Catalog:

5

Inhibitors & Agonists

4

Click Chemistry

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-139286
    Photoclick sphingosine

    Pacsph; PacSphingosine (d18:1)

    		 Biochemical Assay Reagents Others
    Photoclick sphingosine (Pacsph) is a photosensitizing and clickable sphingosine analog. Photoclick sphingosine is metabolized in cells into endogenous lipid metabolic pathways and can be visualized by its clickable alkyne group. Photoclick sphingosine can be used to study intracellular sphingolipid metabolism and subcellular localization .
    Photoclick sphingosine
  • HY-145472
    Sphingosine (d18:1) alkyne

    		Biochemical Assay Reagents Cancer
    Sphingosine (d18:1) alkyne (compound 2b) is an alkyne-labeled Sphingosine (d18:1) that can be used in click chemistry reactions .
    Sphingosine (d18:1) alkyne
  • HY-172653
    Sphingosine-1-phosphate (d18:1) alkyne

    S1P (d18:1) alkyne

    		 Biochemical Assay Reagents Cardiovascular Disease Neurological Disease Inflammation/Immunology Cancer
    Sphingosine-1-phosphate (d18:1) alkyne is an w-alkyne form of sphingosine-1-phosphate. Sphingosine-1-phosphate is a critical regulator of various physiological and pathophysiological processes, such as cancer, atherosclerosis, diabetes and osteroporosis. Sphingosine-1-phosphate can be studied in research for inflammatory diseases, cancer and Alzheimer’s disease .
    Sphingosine-1-phosphate (d18:1) alkyne
  • HY-176102
    C6 Ceramide (d18:1/6:0) alkyne

    N-Hexanoyl-D-erythro-Sphingosine alkyne

    		 Biochemical Assay Reagents Others
    C6 Ceramide (d18:1/6:0) alkyne is an ω-alkyne derivative of C6 ceramide. The terminal alkyne group can be used in click chemistry reactions to tag C6 ceramide with fluorescent or biotinylated labels, allowing the analysis of the metabolism and biological activity of C6 ceramide.
    C6 Ceramide (d18:1/6:0) alkyne
  • HY-134107
    Azido-erythro-sphingosine

    		Biochemical Assay Reagents Others
    Azido-erythro-sphingosines is an intermidate for synthesis of lipid molecules with two hydroxyl groups and a terminal azide group. Azide (N3) group can react with alkyne, BCN, DBCO via Click Chemistry. The hydroxyl groups enable further derivatization or replacement with other reactive functional groups. Azido-erythro-sphingosine is a derivative of Sphingosine, which is a selective inhibitor of protein kinase C activity and phorbol dibutyrate binding in vitro in human platelets.
    Azido-erythro-sphingosine

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