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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3118 | lnp-509 |
Potent and selective ligand of imidazoline 1 receptor (I 1 R)
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| DCC3117 | Ln3844 |
Novel Two-in-One Mutant-Selective Epidermal Growth Factor Receptor Inhibitor That Spans the Orthosteric and Allosteric Sites
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| DCC3116 | Lmptp-in-5d |
Novel highly selective inhibitor of the low-molecular-weight protein tyrosine phosphatase (LMPTP), being highly orally bioavailable and reversing obesity-induced diabetes in mice
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| DCC3115 | lmc-21 |
Novel AI-2 quorum-sensing inhibitor, affecting the starvation response and reducing virulence in several Vibrio species, most likely by interfering with LuxPQ
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| DCC3114 | lm-24 Hydrochloride |
Novel p75NTR antagonist
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| DCC3113 | Lm229 |
Novel Probe for Imaging Tau Pathology in Transgenic Mouse and Rat Models
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| DCC3112 | lm11a-36 |
Negative control for LM11A-24
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| DCC3111 | lm11a-24 |
Novel Modulator of p75NTR-dependent motor neuron death
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| DCC3110 | Lm-030 |
Novel inhibitor of kallikrein-related peptidase 7 (KLK7) and epidermal elastase 2 (ELA2)
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| DCC3109 | Ll4212 |
Novel inducer of biofilm dispersal, having a slower rate of NO release
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| DCC3107 | lk 204-545 |
Highly
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| DCC3106 | Ljp-1586 |
Potent, selective, and orally active inhibitor of semicarbazide-sensitive amine oxidase (SSAO) activity, inhibiting vascular adhesion protein 1 (VAP-1) activity and decreasing the density of macrophages in inflamed atherosclerotic plaques in mice
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| DCC3105 | Lith-o-asp |
Novel pan-inhibitor of sialyltransferase (ST)
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| DCC3104 | lisa-4 |
The first fluorogenic dipeptide probe for
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| DCC3103 | Lipocrine |
The first inhibitor of the catalytic activity of AChE and AChE-induced amyloid-beta aggregation protecting against reactive oxygen species
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| DCC3102 | Lipid Ii Binder 5107930 |
Lipid II binder, causing specific upregulation of the vancomycin-resistance associated gene vraX which is implicated in the cell wall stress stimulon that confers glycopeptide resistance
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| DCC3101 | Lintopride |
5HT-4 antagonist with moderate 5HT-3 antagonist properties
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| DCC3100 | Linker-payload 49 |
Novel Fused Benzodiazepine Hybrid Payload for Antibody-Drug Conjugate (ADC)
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| DCC3099 | Linifolin A |
Natural capsid inhibitor
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| DCC3098 | Lin28-let-7 Inhibitor-1 |
Novel inhibitor of the oncogenic Lin28-let-7 interaction
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| DCC3097 | Liguzinediol |
Potent positive inotropic agent, inhibiting myocardial cell apoptosis
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| DCC3096 | Lifibrate |
Inhibitor of cholinephosphotransferase (CPT), phosphatidyl-N-methylethanolamine N-methyltransferase (PME-NMT), and phosphatidyl-N,N-dimethylethanolamine N-methyltransferase (PDE-NMT)
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| DCC3095 | liarozole Hydrochloride |
Novel inhibitor of AMA1–RON2 interaction, blocking merozoite invasion from schizont-infected RBCs; Cytochrome P450 inhibitor
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| DCC3094 | liafensine |
Serotonin-norepinephrine-dopamine triple reuptake inhibitor (SNDRI); Anti-depressant
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| DCC3093 | L-histidinol Dihydrochloride |
Natural precursor of histamine; reversible inhibitor of protein synthesis
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| DCC3092 | Lh-708 |
Novel inhibitor of cystine stone formation for treatment of cystinuria
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| DCC3091 | Lh65.3 |
Novel S. typhimurium infection inhibitor on the activity of DUSP3, DUSP11, and DUSP27
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| DCC3090 | Lgh447 Hydrochloride |
Potent and specific pan-PIM inhibitor, inhibiting proliferation of several AML cell lines, showing dual antitumoral and bone antiresorptive effects
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| DCC3089 | Lgh00031 |
Novel irreversible inhibitor of cell division cycle 25B, inhibiting human cancer cells via ROS generation
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| DCC3088 | lg190178 |
Novel non-secosteroidal vitamin D receptor (VDR) ligand
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