| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC3187 | Ly-395153 | Allosteric modulator of AMPA receptors |
|
| 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 |
|
| DCC3189 | Ly451646 | AMPA receptor potentiator |
|
| DCC3190 | Ly456236 Hydrochloride | Selective mGlu1 receptor antagonist |
|
| DCC3191 | Ly-465608 | Novel potent and selective dual PPARalpha/gamma agonist |
|
| DCC3192 | Ly-466195 | Novel competitive GLUK5 receptor antagonist |
|
| DCC3193 | Ly544344 | Prodrug of LY354740, highly selective and potent agonist of group II mGlu receptors (mGluR2) |
|
| DCC3194 | Ly-580276 | Novel inhibitor of the type I transforming growth factor beta receptor (TβRI) |
|
| DCC3195 | Lyc-31138 | Novel F1F0-ATPase modulator, significantly decreasing M2 glutamate and increasing M4 glutamate |
|
| 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 |
|
| DCC3197 | Lyngbyastatin 7 | Natural Potent Marine-Derived Elastase Inhibitor |
|
| 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. |
|
| DCC3199 | Lyso-7 | Inhibitor of cyclooxygenase (COX); Pan partial agonist of PPARγ, PPARα and PPARβ/δ |
|
| 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 |
|
| DCC3201 | M-084 Hydrochloride | TRPC4/5 channel blocker, exhibiting antidepressant and anxiolytic effects |
|
| 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 |
|
| DCC3203 | M1-pam-b | Novel selective muscarinic M1 receptor positive allosteric modulator, showed both significant improvement of scopolamine-induced cognitive deficits and severe diarrhea |
|
| DCC3204 | M4k2009 Featured | M4K2209 is a potent, selective BMP type I receptor ALK2 inhibitor with IC50 of 9 nM, >180-fold selective over ALK5 (IC50=2427 nM). |
|
| DCC3205 | M4k2127 | Novel potent and selective ALK2 inhibitor, showing high initial brain uptake, including in the region of interest (pons) |
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| DCC3206 | M4k2163 | Novel CNS Penetrant ALK2 Inhibitor for the Treatment of Diffuse Intrinsic Pontine Glioma |
|
| DCC3207 | M-5mpep | Partial antagonist of mGlu5 |
|
| DCC3208 | M7594_0037 | Novel Peptide Deformylase (PDF) Inhibitor, having inhibitory activity against HeLa, A549 and MCF-7 |
|
| DCC3209 | Mac-0547630 | Novel potent and selective inhibitor of UppS without off-target effects on membrane potential |
|
| DCC3210 | Mac13243 | Novel inhibitor of the bacterial lipoprotein targeting chaperone, LolA |
|
| DCC3211 | Macluraxanthone | Natural immunomodulator, significantly decreasing TNF-α and IL-10 cytokine production, regulating the NF-κB and MAPK signaling pathways, displaying the strongest antiproliferative effects with IC50 values of 2.84 and 0.95 μM against A431 and HeLa cancer c |
|
| DCC3212 | Madtp-372 | Potent and selective inhibitor of the induction of cytopathic effect by CHIKV and VEEV |
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| DCC3213 | Madurmycin | Polyether ionophore antibiotic, inhibiting proliferation and induces apoptosis in myoblast cells |
|
| DCC3214 | Magl-2102 | Novel reversible monoacylglycerol lipase (MAGL) inhibitor |
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| DCC3215 | Magnesium L-threonate | Inhibitor of TNF-α, preventing and restoring memory deficits associated with neuropathic pain |
|
| DCC3216 | Magnesium Oxaloacetate | Inhibitor of the amebicidal activity of activated murine macrophages, helping the parasite to survive within the mouse large intestine and increasing the survival of C. elegans exposed to H2O2 |
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