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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4889 | Srt3025 |
Novel Sirtuin1 Activator, Down-Regulating Sclerostin and Rescuing Ovariectomy-Induced Bone Loss
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| DCC4888 | Sri-39067 |
Novel MOR agonist/DOR antagonist that produced systemically active potent antinociceptive activity in tail-flick assay in mice
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| DCC4887 | Sri-37684 |
Novel GLUT inhibitor, preferentially inhibiting the growth of GBM cells with minimal toxicity to non-neoplastic astrocytes and neurons, also inhibiting glucose uptake and decrease the glycolytic capacity and glycolytic reserve capacity of GBM patient-deri
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| DCC4886 | Sri-37683 |
Novel GLUT inhibitor, preferentially inhibiting the growth of GBM cells with minimal toxicity to non-neoplastic astrocytes and neurons, also inhibiting glucose uptake and decrease the glycolytic capacity and glycolytic reserve capacity of GBM patient-deri
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| DCC4885 | Sri-36160 |
Novel potent inhibitor of Wn/ß-catenin signaling in cancer cells
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| DCC4884 | Sri-35241 |
Novel inhibitor of thrombospondin 1 activation of TGF-β, blocking TGF-β activation (pIC50 = 8.12 nM) and has a plasma half life of 1.8 h (iv)
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| DCC4883 | Sri-31040 |
Potent DAT allosteric modulator, partially inhibiting DAT uptake without altering DAT-mediated reverse transport and with minimal inhibition of DAT binding
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| DCC4882 | Sri-29132 |
Highly blood-brain barrier permeant, potent, and selective for LRRK2 kinase activity, being effective in attenuating pro-inflammatory responses in macrophages and rescuing neurite retraction phenotypes in neurons.
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| DCC4881 | Sri-22138 |
Novel mixed μ opioid receptor (MOR) agonist and δ/κ opioid receptor (DOR/KOR) antagonist
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| DCC4880 | Srebp-in-dhg |
Novel inhibitor of sterol regulatory element-binding protein (SREBP), impairing the SREBP activity by inhibiting glucose transporters and thereby activating AMP-activated protein kinase (AMPK)
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| DCC4879 | Srctide |
Peptide substrate for many protein kinases, such as Blk, BTK, cKit, EPHA1, EPHB2, EPHB3, ERBB4, FAK, Flt3, IGF-1R, ITK, Lck, MET, MUSK, Ret, Src, TIE2, TrkB, VEGF-R1 (Flt-1) and VEGF-R2 (KDR)
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| DCC4878 | Sr8185 |
Novel Selective TBK1/IKK dual inhibitor with anticancer potency
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| DCC4877 | Sr-58611a |
The first selective β3 adrenergic agonist, showing to possess a profile of antidepressant activity in rodents
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| DCC4876 | Sr-43845 |
Novel renin inhibitor
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| DCC4875 | Sr-4326 |
Novel Inhibitor of c-Jun N-terminal Kinase 3 (JNK3)
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| DCC4874 | Sr-3737 |
Potent inhibitor of both JNK3 and p38
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| DCC4873 | Sr24237 |
Novel NR4A nuclear receptor modulator
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| DCC4872 | Sr2067 |
Novel partial agonist of PPARgamma
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| DCC4871 | Sr-17398 Hydrochloride |
Novel Unc-51-Like Kinase 1 (ULK1)
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| DCC4870 | Sr142948a |
Selective neurotensin antagonist
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| DCC4869 | Sr10658 |
Novel NR4A nuclear receptor modulator
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| DCC4868 | Sr10098 |
Novel NR4A nuclear receptor modulator
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| DCC4867 | Sr-01000634273-1 |
Novel inhibitor of the in vivo aggregation of
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| 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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