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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC3206 | M4k2163 |
Novel CNS Penetrant ALK2 Inhibitor for the Treatment of Diffuse Intrinsic Pontine Glioma
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| DCC3205 | M4k2127 |
Novel potent and selective ALK2 inhibitor, showing high initial brain uptake, including in the region of interest (pons)
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| DCC3203 | M1-pam-b |
Novel selective muscarinic M1 receptor positive allosteric modulator, showed both significant improvement of scopolamine-induced cognitive deficits and severe diarrhea
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| DCC3202 | M1-pam-a |
Novel selective muscarinic M1 receptor positive allosteric modulator, significantly improved scopolamine-induced cognitive deficits without prominent signs of diarrhea at up to 1000 mg/kg in mice
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| DCC3201 | M-084 Hydrochloride |
TRPC4/5 channel blocker, exhibiting antidepressant and anxiolytic effects
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| DCC3200 | Lzz-02 |
Novel inhibitor of the transcriptional activity of β-catenin, degrading the expression of β-catenin by stabilizing axin 2 and diminishing downstream proteins levels, including c-Myc and cyclin D1, effectively shrinking tumor xenograft derived from colonic
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| DCC3199 | Lyso-7 |
Inhibitor of cyclooxygenase (COX); Pan partial agonist of PPARγ, PPARα and PPARβ/δ
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| DCC3198 | Lysine Orotate |
Inhibitor of viral replication, especially useful in the treatment of the Herpes family of viruses which includes Herpes Simplex 1 and 2 , EBV , CMV and Varicella.
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| DCC3197 | Lyngbyastatin 7 |
Natural Potent Marine-Derived Elastase Inhibitor
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| DCC3196 | Ly-hn2am |
Nove fluorescent probe for highly sensitive monitoring drug induced lysosomal pH value changes, exhibiting good biological compatibility, low cytotoxicity and high resistance to photobleaching
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| DCC3195 | Lyc-31138 |
Novel F1F0-ATPase modulator, significantly decreasing M2 glutamate and increasing M4 glutamate
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| DCC3194 | Ly-580276 |
Novel inhibitor of the type I transforming growth factor beta receptor (TβRI)
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| DCC3193 | Ly544344 |
Prodrug of LY354740, highly selective and potent agonist of group II mGlu receptors (mGluR2)
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| DCC3192 | Ly-466195 |
Novel competitive GLUK5 receptor antagonist
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| DCC3191 | Ly-465608 |
Novel potent and selective dual PPARalpha/gamma agonist
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| DCC3190 | Ly456236 Hydrochloride |
Selective mGlu1 receptor antagonist
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| DCC3189 | Ly451646 |
AMPA receptor potentiator
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| DCC3188 | Ly444711 |
Orally active ghrelin agonist, bindjng with high affinity to and being a potent activator of the growth hormone secretagogue receptor 1a (GHS-R1a) receptor
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| DCC3187 | Ly-395153 |
Allosteric modulator of AMPA receptors
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| DCC3186 | Ly392098 |
AMPA receptor potentiator
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| DCC3185 | Ly382884 |
Selective GluR5 kainate receptor antagonist
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| DCC3184 | Ly339434 |
Potent GluR5 kainate receptor agonist
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| DCC3183 | Ly-333531 Mesylate |
Potent and selective inhibitor of PKCβI and PKCβII
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| DCC3182 | Ly2979165 Ammonium Salt |
Novel highly potent and selective agonist of metabotropic glutamate (mGlu) receptors 2 and 3
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| DCC3180 | Ly2934747 |
Novel, potent, and systemically bioavailable mGlu2/3 receptor agonist, exhibiting both antipsychotic and analgesic properties in vivo
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| DCC3179 | ly2886721 Hydrochloride |
Orally active cell-permeable inhibitor of human
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| DCC3178 | Ly-278584 |
Potent 5-HT3 serotonin receptor antagonist
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| DCC3177 | Ly2389575 |
Selective negative allosteric modulator of mGlu3
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| DCC3176 | Ly-231617 |
Potent antioxidant, being cytoprotective in models of focal and global cerebral ischemia
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| DCC3175 | ly-2140023 |
Novel mGlu2/3 receptor agonist; Prodrug of LY-404039
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