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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC11995 | BI 703704 |
A novel potent soluble guanylate cyclase (sGC) activator.
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| DC11663 | GS-5759 |
A novel bifunctional PDE4 inhibitor (IC50=5 nM) and long acting β2-adrenoceptor agonist (EC50=8 nM).
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| DC11522 | Imarikiren hydrochloride |
A highly potent, selective, orally active renin inhibitor with IC50 of 2.1 nM in hPRA assay.
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| DC11936 | TAK-915 |
A highly potent, selective, brain-penetrating and orally active phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 0.61 nM.
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| DC11537 | AD-35 phosphate |
A donepezil analog that can moderately inhibit acetylcholinesterase and metal-induced Aβ aggregation in vitro and shows disassembly of Aβ aggregates.
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| DC11539 | AD-35 hydrochloride |
A donepezil analog that can moderately inhibit acetylcholinesterase and metal-induced Aβ aggregation in vitro and shows disassembly of Aβ aggregates.
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| DC11538 | AD-35 |
A donepezil analog that can moderately inhibit acetylcholinesterase and metal-induced Aβ aggregation in vitro and shows disassembly of Aβ aggregates.
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| DCS-019 | (-)-Huperzine A |
>98%,Standard References
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| DC9581 | (S)-(+)-Rolipram |
(S)-(+)-Rolipram is a PDE4-inhibitor and an anti-inflammatory agent, less potent than its R enantiomer.
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| DC9584 | (R)-(-)-Rolipram |
(R)-(-)-Rolipram is a potent and cAMP-specific PDE4 inhibitor with IC50 of 0.22 uM; 2.5-fold more potent than (+)-rolipram (IC50= 2.58 uM) in inhibiting membrane-bound PDE 4.
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