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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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