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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC0781 | Atsp-7041 |
Novel potent and selective dual inhibitor of MDM2 (Ki = 0.9 nM) and MDMX (Ki = 7 nM)
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| DCC0780 | Atsp-3900 |
Novel Potent Dual Inhibitor of MDM2 and MDMX (Ki =1 nM)
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| DCC0779 | Atromentin |
Natural potent apoptosis inducer in U937 cells, inducing caspase-3 processing, PARP, and DNA fragmentation
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| DCC0778 | atqthb |
Novel antitimor agent, exhibiting superior anti-proliferative activity, excellent chemo-sensitizing activity against pancreatic cancer in vitro and in combination with Gemcitabine
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| DCC0777 | Atp-alpha-ch2-gamma-thio |
Novel potent inhibitor of nucleotide pyrophosphatase/phosphodiesterase-1 (NPP1)
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| DCC0776 | a-tocopheryl 2,3,5-triiodobenzoate |
Novel non-toxic contrast agent for micro-CT imaging
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| DCC0775 | Atm-1001 |
Novel inhibitor of the cancer-associated tropomyosin 3.1 (Tpm3.1), suppressing glucose-stimulated insulin secretion (GSIS) from the pancreatic islets
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| DCC0774 | Atl802 |
Novel selective A2BR antagonist
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| DCC0773 | Atiprimod Dimaleate |
Potent JAK2 inhibitor
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| DCC0772 | Atenolol Hydrochloride |
Selective ß1 receptor antagonist
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| DCC0771 | Atd-3169 |
Novel ROS generator, permeating mycobacteria to reliably enhance endogenous ROS including superoxide radical
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| DCC0770 | Atcaa-1 |
Potent cytotoxic agent for both prostate cancer and melanoma
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| DCC0769 | Atb-345 |
Hydrogen sulfide-releasing cyclooxygenase inhibitor
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| DCC0767 | Atag2139 |
Novel degrader of MTH1 fusion proteins for use within the aTAG system
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| DCC0766 | At7519m |
Novel inhibitor of cyclin-dependent kinases 1, 2, 4, 5, and 9 with in vitro activity against lymphoid malignancies
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| DCC0765 | At-312 |
Novel selective nociceptin receptor (NOP) agonist
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| 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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