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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4866 | Spu-106 |
Novel specific PAK4 inhibitor, effectively inhibiting the invasion of SGC7901 cells without cytotoxicity, regulating the PAK4/LIMK1/cofilin and PAK4/SCG10 signaling pathways
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| DCC4865 | Sptssb-binder-18 |
Novel potent and selective binder of small subunit B of the serine palmitoyltransferase complex (SPTSSB)
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| DCC4864 | Spt-in-1 |
Novel potent serine palmitoyl transferase (SPT) inhibitor
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| DCC4863 | Spop-in-6lc |
Novel SPOP inhibitor, suppressing the viability and inhibiting the colony formation of ccRCC cell lines driven by cytoplasmic SPOP
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| DCC4862 | Spongosine |
Pivotal intercellular signal transmitter
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| DCC4861 | spongiacidin C |
USP7 inhibitor from the marine sponge Stylissa massa
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| DCC4860 | Spmtrien |
Novel isosteric charge-deficient spermine analogue
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| DCC4859 | Spla2 Inhibitor Pyr-1 |
Novel potent sPLA2 inhibitor, selectively targeting hGIIA and hGIID
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| DCC4858 | Spiroxamine |
Sterol Biosynthesis Inhibitor, Fungicide
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| DCC4857 | Spirooxindole 1a |
Novel p53 Stabilizer for Brain Cell Differentiation
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| DCC4856 | Spirohydantoin-21 |
Novel selective orally bioavailable inhibitor of p300/CBP histone acetyltransferase
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| DCC4855 | Spi-1865 |
Novel gamma-secretase modulator
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| DCC4854 | Spectinomycin Dihydrochloride |
Antibiotic, binding to the bacterial 30S ribosomal subunit, interfering with the initiation of protein synthesis and with proper protein elongation and leading to bacterial cell death
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| DCC4853 | Spectinamide-1599 |
Novel anti-tuberculosis agent against intracellular Mycobacterium tuberculosis
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| DCC4852 | Spd-2-am |
Novel photo-controllable hydrogen sulfide donor applicable in live cells
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| DCC4851 | SPB08007 |
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| DCC4850 | spb03924 |
Novel telomerase inhibitor
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| DCC4849 | Spam (signal Peptide-based Affinity Maturated Ligand) |
Novel Programmed Death Ligand 1 (PD-L1) Binding Peptide (a Peptide Ligand for PD-L1)
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| DCC4848 | Sortin3 Maleate |
Sorting inhibitor, blocking Vps16 function, one protein in the class C tethering complex, and increasing aflatoxin synthesis and export
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| DCC4847 | sori-9804 |
Novel partial inhibitor of amphetamine-induced dopamine release
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| DCC4846 | sori-20041 |
DAT modulator, being unique in affecting substrate uptake without impacting efflux
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| DCC4845 | soraphinol A |
Human norepinephrine transporter blocker
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| DCC4844 | Sophoraflavanone B |
Natural inhibitor of the Kv1.3 channels in a concentration-dependent manner
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| DCC4843 | Sophorafavanone A |
Inhibitor of constitutive and inducible STAT3 activation through the activation of SHP-2 tyrosine phosphatase
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| DCC4842 | Sophoradin |
Natural analgesic, antipyretic, anti-inflammatory, and anti-tumor agent
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| DCC4841 | Sonedenoson |
A2A adenosine receptor agonist
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| DCC4840 | Somcl-863 |
Novel, selective and orally bioavailable c-Met inhibitor, exhibiting antitumor activity both in vitro and in vivo
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| DCC4839 | Somcl-668 |
Novel potent and selective allosteric modulator of sigma-1 receptor
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| DCC4838 | Somatoprim |
Unique somatostatin receptor subtypes 2-, 4- and 5-selective analogue, effectively reducing GH secretion in human GH-secreting pituitary adenomas even in Octreotide non-responsive tumours.
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| DCC4837 | Somapacitan |
Novel long-acting, reversible albumin-binding growth hormone (GH) derivative for treatment of growth hormone dificiency
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