Vinburnine

Biochem/physiol Actions An analog of myristic acid that becomes metabolically activated in cells to form 2-hydroxymyristoyl-CoA. Inhibitor of protein myristoylation.

A potent cell-permeable and reversible inhibitor of glycogen synthase kinase-3&#946 (IC 50 = 230 nM), Lck (IC 50 = 470 nM), and cyclin-dependent kinases (Cdks). Inhibits Cdk1/cyclin B (IC 50 = 400 nM), Cdk2/cyclin A (IC 50 = 680 nM), Cdk2/cyclin E

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A cell-permeable triazine based compound that inhibits Ca 2+ -dependent fusion of lysosomes with the plasma membrane and the release of lysosomal content, without affecting enlargeosomes or other membrane-bound organelles. It does not disturb the

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034 . This CRM is traceable to primary material from an NMI, e.

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Indole alkaloid that binds to tubulin, inhibiting formation of microtubules. Depolymerizes microtubules.