Hymenialdisine-[d4]

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Purity: 95%

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(4Z)-4-(2-Amino-1,5-dihydro-5-oxo-4H-imidazol-4-ylidene)-2-bromo-4,5,6,7-tetrahydro-pyrrolo[2,3-c]azepin-8(1H)-one-d4 (Z)-Hymenialdisine-d4

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Hymenialdisine-[d4] is an isotopically labelled analogue of Hymenialdisine. A potent inhibitor of a variety of kinases including MEK-1, GSK-3Β, and CKI. It also exhibits inhibition of the G2 cell cycle checkpoint at the micromolar concentrations. A marine sponge alkaloid, a natural product.

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