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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC0764 | At-265 |
Nucleosidic antibiotic
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| DCC0763 | At-121 |
Novel dual μ-opioid and nociceptin receptor partial agonist (K i = 16.49 and 3.67 nM, respectively)
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| DCC0762 | At-1012 |
High affinity, selective alpha3beta4 nAChR ligand
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| DCC0761 | At-1001 |
Novel potent and selective partial agonist of human and rat α3β4 nicotinic cholinergic receptors
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| DCC0760 | At-089 |
Novel NOP receptor-mu opioid receptor ligand
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| DCC0759 | At-076 |
The First Small-molecule Opioid Pan Antagonist with Nanomolar Affinity at Mu, Delta, Kappa and Nociceptin Opioid Receptors.
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| DCC0758 | asyn-in-576755 |
Novel inhibitor of αSyn fibrillization, blocking fibril growth and suppressing A53T αSyn neurotoxicity
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| DCC0757 | Asymmetric Dimethylarginine |
Natural endogenous inhibitor of nitric oxide synthases (NOS), also inhibiting arginine transport and increasing oxygen free radicals, mitochondrial dysfunction and transforming growth factor beta (TGFβ) expression, exhibiting a strong association with car
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| DCC0756 | asterriquinone |
Inhibitor of HIV-reverse transcriptase activity
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| DCC0755 | Ast7062601 |
Novel AKAP1/PKA modulator, inducing UCP1 expression and thermogenesis
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| DCC0754 | Aß-in-10 |
Novel anti-Alzheimer’s agent, inhibiting amyloid β aggregation, β-secretase, and tau aggregation
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| DCC0753 | Aß/tau Probe 18 |
Novel near-infrared (NIR) probe for imaging β-amyloid (Aβ) plaques or Tau tangles
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| DCC0752 | Asr352 |
Novel potent anticancer agent, inhibiting the growth of CRC bulk and sensitized FOLFOX-resistant cells
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| DCC0751 | Aspulvinone H |
Natural inhibitor of glutamic oxaloacetate transaminase 1 (GOT1), suppressing glutamine metabolism, making PDAC cells sensitive to oxidative stress and inhibiting cell proliferation, exhibiting potent in vivo antitumor activity in an SW1990-cell-induced x
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| DCC0750 | Aspulvinone E |
Natural luciferase inhibitor
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| DCC0749 | Aspterric Acid |
Natural inhibitor of pollen development in Arabidopsis thaliana, also inhibiting dihydroxy-acid dehydratase (DHAD)
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| DCC0748 | Asperphenamate |
Natural antineoplastic agent, targeting cathepsin and inducing autophagy effects in breast cancer cells
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| DCC0747 | Asperlicin D |
Novel cholecystokinin antagonist
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| DCC0746 | asperlicin C |
Novel cholecystokinin antagonist
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| DCC0745 | asperlicin |
Selective antagonist for the cholecystokinin receptor CCKA
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| DCC0744 | Asp9726 |
Novel potent Aspergillus hyphal growth inhibitor
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| DCC0743 | Asp9133 |
Novel long-acting muscarinic antagonist (LAMA), showing more selective inhibition of bronchoconstriction against salivation and more rapid onset of action than tiotropium bromide
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| DCC0742 | Asp-7962 |
Novel tropomyosin-related kinase A (TrkA) inhibitor for the oral treatment of pain due to osteoarthritis of the knee
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| DCC0741 | Asp5854 |
Novel dual A2A/A1 AR antagonist
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| DCC0740 | Asp2397 |
Novel antifungal agent against Aspergillus isolates
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| DCC0739 | Asoprisnil |
Selective progesterone receptor modulator
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| DCC0738 | Asns-in-1 |
Novel slow-onset, tight binding, potent asparagine synthetase (ASNS) inhibitor
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| DCC0737 | Asn06917370 |
Novel potent GPR17 agonist
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| DCC0736 | Asn008 |
Novel Permanently-charged Sodium Channel Blocker, Showing Robust Efficacy, a Rapid Onset and Long Duration of Action
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| DCC0735 | Asm-in-21b |
Novel, Potent, Selective, and Direct Acid Sphingomyelinase (ASM) Inhibitor with Antidepressant Activity
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