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5.08739 | InSolution, ≥98% | |||
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8.52034 | Novabiochem® | |||
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371970 | A cell-permeable, reversible, and ATP-competitive Ca2+ antagonist with anti-vasospastic properties. | |||
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410957 | A cell-permeable, non-specific inhibitor of cAMP and cGMP phosphodiesterases (IC₅₀ = 2-50 µM). | |||
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5.04744 | InSolution, ≥98%, 30 mM in DMSO, A cell-permeable tetracyclic diterpene antibiotic | |||
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568500 | Cell-permeable adenylate cyclase inhibitor. | |||
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474502 | Ultrasensitive, fluorogenic substrate for assays of N-acetyl-β-D-glucosaminidase. | |||
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116812 | Cell-permeable cAMP analog that activates both protein kinase A and protein kinase G. | |||
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203820 | Cell-permeable cGMP analog that is more resistant to phosphodiesterases than cGMP. | |||
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574625 | A reversible and competitive inhibitor of protein tyrosine phosphatases. | |||
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I5523 | powder, ≥27 USP units/mg | |||
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8.52030 | Novabiochem® | |||
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324693 | Principal alkaloid of ipecac, isolated from the ground roots of Uragoga ipecacuanha. | |||
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557502 | A cell-permeable, selective inhibitor of cAMP-specific phosphodiesterase (PDE IV; IC₅₀ = 2 µM). | |||
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SML3093 | ≥98% (HPLC) | |||
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609218 | 98 atom % 15N | |||
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5.05412 | ||||
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616387 | Irreversible inhibitor of chymotrypsin. | |||
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551850 | A non-specific phospholipase A2 (PLA2) inhibitor. | |||
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203800 | Cell-permeable cAMP analog that has greater resistance to phosphodiesterases than cAMP. | |||
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538903 | Activates adenylate cyclase activity via a G-protein coupled receptor. | |||
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487870 | Substrate for the colorimetric assay of β-D-xylosidase. Also shown to disrupt proteoglycan biosynthesis in vivo. | |||
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490075 | 98 atom % 15N | |||