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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC43839 | Viscidulin II |
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| DC43838 | Viscidulin III |
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| DC43837 | 12-O-Tiglylphorbol-13-isobutyrate |
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| DC43836 | TNFalpha-IN-S10 |
Novel Inhibitor of TNF-α
More description
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| DC43835 | SC-144 Hydrochloride |
Novel orally active glycoprotein 130 (gp130) inhibitor
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| DC43834 | Zingiberen newsaponin |
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| DC43833 | BGT-226 |
A phosphatidylinositol 3-kinase (PI3K) inhibitor
More description
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| DC43832 | VUF10661 |
Partial agonist in CXCR3-mediated chemotaxis, bound to CXCR3 in an allosteric fashion with the same efficacy as CXCL11
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| DC43830 | Lobelin |
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| DC43827 | ML262 |
Potent inhibitor of lipid droplet formation
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| DC43826 | beta-Rhamnocitrin |
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| DC43825 | ML170 |
Highly specific allosteric activator for the tumor-specific isoform of human pyruvate kinase (M2 isoform)
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| DC43824 | 2,3,24-Trihydroxy-12-ursen-28-oic acid |
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| DC43822 | Chamaejasmenin C |
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| DC43821 | Mogroside VI |
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| DC43820 | Chiisanoside |
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| DC43819 | UBP551 |
Selective modulator of NMDA receptors, potentiates responses at GluN1/GluN2D
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| DC43818 | IPR-803 |
Inhibitor of the uPAR·uPA protein-protein interaction, blocking cancer cell invasion
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| DC43817 | AMG-51 |
A selective inhibitor of c-Met kinase
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| DC43816 | Mogroside IIe |
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| DC43815 | Isogambogenic acid |
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| DC43814 | Cerebroside B |
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| DC43813 | M8-B |
Selective and potent antagonist of the transient receptor potential melastatin-8 (TRPM8) channel
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| DC43811 | Alismol |
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| DC43809 | S(-)-Cyanopindolol hemifumarate |
5-HT1A/1B serotonin receptor antagonist; β3-adrenoceptor antagonist
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| DC43808 | SV-156 |
Highly selective D2 dopamine receptor antagonist
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| DC43807 | Isoneochamaejasmine A |
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| DC43806 | 5-Hydroxy-1,7-diphenyl-6-hepten-3-one |
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| DC43805 | A-839977 |
Potent P2X7 antagonist blocking BzATP-evoked calcium influx
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| DC43803 | threo-Guaiacylglycerol beta-coniferyl ether |
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