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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3134 | Lqmed 330 |
Novel potent and specific inhibitor of O-linked β-N-acetylglucosamine transferase (OGT)
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| DCC3133 | Lqfm030 |
Novel p53 activator through the inhibition of MDM2
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| DCC3132 | Lpa1-3 Agonist Cpy |
Novel LPA 1-3 agonist, inducing a calcium response in hLPA 1-3 cells within a range of 0.4 to 1.5-log lower potency, as compared to LPA
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| DCC3131 | Lpa1-3 Agonist Cpx |
Novel LPA 1-3 agonist, inducing a calcium response in hLPA 1-3 cells within a range of 0.4 to 1.5-log lower potency, as compared to LPA
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| DCC3130 | Lp-925219 |
Novel inhibitor of both renal SGLT1 and SGLT2
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| DCC3129 | Lp-922761 |
Novel potent and selective peripheral AAK1 inhibitor
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| DCC3128 | Lp-261 |
Potent antimitotic and oral tubulin binding agent, significantly inhibiting growth of a human non-small-cell lung tumor
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| DCC3127 | Lp-20 Hydrochloride |
Potent ligand of the 5-HT7 receptor
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| DCC3126 | Lox-activity Sensor-1 |
Novel LOX-activity sensor for cross-linking with a collagen peptide to chemoselectively target endogenous aldehydes generated by LOX
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| DCC3125 | Lopinavir M-3/m-4 |
Lopinavir Secondary Metabolite
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| DCC3124 | Loperamide |
Opioid receptor agonist, acting on the µ-opioid receptors in the myenteric plexus of the large intestine
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| DCC3123 | Longanlactone |
Natural neurotrophic agent
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| DCC3122 | Lomefloxacin |
Antibiotic for treatment of bacterial infections including bronchitis and urinary tract infections, prevent urinary tract infections prior to surgery
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| DCC3121 | Lobelane Hydrochloride |
Inhibitor of the Vesicular_monoamine_transporter_2>vesicular monoamine transporter-2 (VMAT2)
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| DCC3119 | Lnp599 Hydrochloride |
Novel potent and specific agonist of I 1 imidazoline receptors
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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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