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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC3016 | Lanopepden Mesylate |
Novel Peptide Deformylase Inhibitor against Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus aureus
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| DCC3015 | la-mem |
Glutamate receptor antagonist and radical scavenging agent
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| DCC3014 | Lamellarin D |
Top1mt inhibitor, targeting mitochondrial DNA
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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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| 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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| DCC3011 | L-870812 |
Novel inhibitor of HIV-1 and SIV integrase
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| DCC3010 | L-858051 |
Chemically-modified forskolin with greater stability and water solubility than the parent compound
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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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| DCC3007 | L-770644 |
Potent and selective agonist of the human beta3 adrenergic receptor
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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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| DCC3005 | L-749329 |
Dual ET(A)/ET(B) endothelin receptor antagonist
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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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| DCC3003 | L-739758 |
Potent glycoprotein IIb/IIIa inhibitor
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| DCC3002 | L-735821 |
Inhibitor of the KCNQ1 channel
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| DCC3001 | L-731988 |
Inhibitor of Strand Transfer, Preventing Integration and Inhibiting HIV-1 Replication in Cells
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| DCC3000 | L-708906 |
Inhibitor of Human Immunodeficiency Virus Type 1 (HIV-1)
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| DCC2999 | L-696229 |
HIV-1 non-nucleoside reverse transcriptase inhibitor
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| DCC2998 | L-687306 |
Novel partial agonist of muscarinic M1 receptors
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| DCC2997 | L-682679 |
HIV protease inhibitor
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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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| DCC2995 | L-663581 |
Novel partial agonist of the benzodiazepine receptor
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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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| DCC2993 | L-651392 |
Potent leukotriene inhibitor
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| DCC2992 | L61h46 |
Novel potent inhibitor of human pancreatic cancer cells
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| DCC2991 | L524-0366 |
Novel inhibitor of the TWEAK-Fn14 signaling cascade
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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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| 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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| 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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| 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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| DCC2986 | L-162782 |
Nonpeptide agonist of angiotensin AT1 receptor
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