5 Results for "

Sphingosine alkyne

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "Sphingosine alkyne" in MCE Product Catalog:

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Cat. No.: HY-145472
CAS No.: 954096-91-4
Research Areas:  

Cancer

Sphingosine (d18:1) alkyne (compound 2b) is an alkyne-labeled Sphingosine (d18:1) that can be used in click chemistry reactions .
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Cat. No.: HY-139286
CAS No.: 1823021-14-2
Synonyms: Pacsph; PacSphingosine (d18:1)
Research Areas:  

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 .
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Cat. No.: HY-172653
Synonyms: S1P (d18:1) alkyne
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 .
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Cat. No.: HY-176102
Synonyms: N-Hexanoyl-D-erythro-Sphingosine alkyne
Research Areas:  

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.
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Cat. No.: HY-134107
CAS No.: 103348-49-8
Research Areas:  

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.
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