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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2986 | L-162782 | Nonpeptide agonist of angiotensin AT1 receptor |
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| DCC2987 | L17er4 | Novel cell-permeable attenuated cationic amphiphilic lytic (ACAL) peptide, efficiently bring immunoglobulin G (IgG) and other functional proteins into cells |
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| DCC2988 | L2-4048 | Novel Migration Inhibitory Factor (MIF) inhibitor, binding at the allosteric and tautomerase sites, blocking MIF's tautomerase CD74 receptor binding, and pro-inflammatory activities |
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| DCC2989 | L458-bpyne | Novel γ-secretase modulator photoaffinity probe, identifying distinct allosteric binding sites on presenilin that can be exploited to reduce levels of pathogenic Aβ species |
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| DCC2990 | L465046 (α-synuclein Amyloid Aggregation Inhibitor) | Novel inhibitor of α-synuclein amyloid aggregation for the treatment of Parkinson's disease |
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| DCC2991 | L524-0366 | Novel inhibitor of the TWEAK-Fn14 signaling cascade |
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| DCC2992 | L61h46 | Novel potent inhibitor of human pancreatic cancer cells |
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| DCC2993 | L-651392 | Potent leukotriene inhibitor |
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| DCC2994 | L-658758 | Blocker of the activity of human neutrophil elastase (NE), human proteinase-3, human macrophage metalloelastase, mouse macrophage metalloelastase and Pseudomonas aeruginosa elastase |
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| DCC2995 | L-663581 | Novel partial agonist of the benzodiazepine receptor |
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| DCC2996 | L-680833 | Potent, orally active monocyclic beta-lactam inhibitor of human polymorphonuclear leukocyte elastase (PMNL-E) |
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| DCC2997 | L-682679 | HIV protease inhibitor |
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| DCC2998 | L-687306 | Novel partial agonist of muscarinic M1 receptors |
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| DCC2999 | L-696229 | HIV-1 non-nucleoside reverse transcriptase inhibitor |
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| DCC3000 | L-708906 | Inhibitor of Human Immunodeficiency Virus Type 1 (HIV-1) |
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| DCC3001 | L-731988 | Inhibitor of Strand Transfer, Preventing Integration and Inhibiting HIV-1 Replication in Cells |
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| DCC3002 | L-735821 | Inhibitor of the KCNQ1 channel |
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| DCC3003 | L-739758 | Potent glycoprotein IIb/IIIa inhibitor |
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| DCC3004 | L-744832 | Ras farnesyltransferase inhibitor, inhibiting in p70(s6k) phosphorylation in mammary tumors, inducing tumor regression in transgenic mice by mediating alterations in both cell cycle control and apoptosis |
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| DCC3005 | L-749329 | Dual ET(A)/ET(B) endothelin receptor antagonist |
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| DCC3006 | L-768673 | Class III antiarrhythmic agent, selectively blocking the slowly activating cardiac delayed rectifier potassium current Iks |
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| DCC3007 | L-770644 | Potent and selective agonist of the human beta3 adrenergic receptor |
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| DCC3008 | L-778123 Featured | L-778123 is a dual FPTase and GGPTase-I inhibitor, with IC50s of 2 nM and 98 nM respectively. |
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| DCC3009 | L-841411 | Novel HIV-1 integrase strand transfer inhibitor (INSTI), stabilizing an integrase-single blunt-ended DNA complex |
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| DCC3010 | L-858051 | Chemically-modified forskolin with greater stability and water solubility than the parent compound |
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| DCC3011 | L-870812 | Novel inhibitor of HIV-1 and SIV integrase |
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| DCC3012 | L-94901 | The first organ-selective thyromimetic, lowering plasma low density lipoprotein (LDL) cholesterol and raising plasma high density lipoprotein (HDL) cholesterol levels |
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| DCC3013 | L-97-1 | Adenosine A1 receptor antagonist, reducing allergic responses to house dust mite in an allergic rabbit model of asthma, improving survival and protecting the kidney in a rat model of cecal ligation and puncture induced sepsis, also improving survival and |
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| DCC3014 | Lamellarin D | Top1mt inhibitor, targeting mitochondrial DNA |
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| DCC3015 | la-mem | Glutamate receptor antagonist and radical scavenging agent |
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