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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC3076 | Leo-29102 |
Novel Soft-Drug Inhibitor of Phosphodiesterase 4 (PDE4) for Topical Treatment of Atopic Dermatitis
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| DCC3075 | Leo-134310 |
Novel non-steroidal glucocorticoid receptor agonist
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| DCC3074 | Leniquinsin |
Phosphodiesterase inhibitor, acting as a vasodilator and showing antihypertensive effects
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| DCC3073 | Lenalidomide-slf |
Novel Electrophilic PROTAC that degrades nuclear proteins by engaging DCAF16
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| DCC3072 | Lenaldekar |
Novel inhibitor of T-cell expansion and autoimmune encephalomyelitis
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| DCC3071 | Lem-06 |
Novel inhibitor of nuclear receptor binding SET domain 2 (NSD2), against H3K36 methylation
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| DCC3070 | Lei-301 |
Novel potent inhibitor for the PLAAT family members, reducing the NAE levels, including anandamide, in cells overexpressing PLAAT2 or PLAAT5
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| DCC3069 | Lei-101 |
Novel, orally available and peripherally restricted selective cannabinoid CB2 receptor agonist
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| DCC3068 | Lefucoxib |
Cyclooxygenase-2 (COX-2) inhibitor
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| DCC3067 | Ledgf/p75-in Inhibitor-6d |
Novel inhibitor of the LEDGF/p75-IN interaction, potently inhibiting both the early and late stages of HIV-1 replication
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| DCC3066 | Ldt8 Dihydrochloride |
Highly potent multi-target antagonists of alpha1A- and alpha1D-adrenoceptors, and 5-HT1A receptors
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| DCC3065 | Ldt5 Dihydrochloride |
Highly potent multi-target antagonists of both alpha1A- and alpha1D-adrenoceptors, and also of 5-HT1A receptors
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| DCC3064 | Ldt409 |
Novel partial agonist of PPARα and PPARγ, providing distinct and favorable gene activation profiles for the treatment of diabetes and obesity
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| DCC3063 | Ldt3 Dihydrochloride |
Highly potent multi-target antagonists of both alpha1A- and alpha1D-adrenoceptors, and also of 5-HT1A receptors
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| DCC3062 | Lds-751 |
Nucleic acid binding fluorescent dye
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| DCC3061 | L-dopa-snme3 |
Precursor of 6-[18F]Fluoro-L-DOPA used for positron emission tomography (PET) scans. References: http://www.hindawi.com/journals/bmri/2014/674063/
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| DCC3060 | Ldn-73794 |
Competitive LRRK2 kinase inhibitor without affecting the GTPase activity
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| DCC3059 | Ldn-213844 |
Novel ALK2 inhibitor
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| DCC3058 | ldn-211898 |
Potent haspin kinase inhibitor
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| DCC3057 | Ldn-193665 |
Novel potent tau kinase inhibitor, targeting CDK5/p25 and GSK3β
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| DCC3056 | ldn-193594 |
Novel cdk5/p25 kinase inhibitor
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| DCC3055 | ldn-193191 |
Potent and metabolically stable inhibitor of necroptosis, a regulated caspase-independent cell death pathway
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| DCC3054 | Ldn-193188 |
Novel inhibitor of phosphatidylcholine transfer protein (PC-TP)
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| DCC3053 | ldn-112006 |
Necroptosis inhibitor
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| DCC3052 | Ldn-0130436 |
Novel TDP-43::GFP aggregation inhibitor
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| DCC3051 | Ldn-0070977 |
Novel inhibitor of PERK stress-dependent eIF2α phosphorylation with no toxicity to the cells
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| DCC3050 | Ldn-0044878 |
Novel PAK3 kinase inhibitor, inhibiting p53-inactivated cancers
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| DCC3049 | Ldn-0028574 |
Novel Inhibitor of SIRT1; Inhibitor of the human MDM2-p53 interaction
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| DCC3048 | Ldha-in-22y |
Novel inhibitor of human lactate dehydrogenase A (LDHA)
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| DCC3047 | Lddn-0003499 |
Novel Src family tyrosine kinase inhibitor with anti-inflammatory effects in response to Aß stimulation of microglia
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