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A derivative of Sphingosine that is a selective inhibitor of protein kinase C activity and phorbol dibutyrate binding in vitro in human platelets. This compound does not inhibit protein kinase A or myosin light chain kinase, but does inhibit calmodulin-dependent enzymes.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-O-(tert-Butyldimethylsilyloxy)-2-Fmoc-erythro-sphingosine, 10 mg | sc-206670 | 10 mg | $380.00 |