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Cat. No. Product Name Field of Application Chemical Structure
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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