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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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