| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4848 | Sortin3 Maleate | Sorting inhibitor, blocking Vps16 function, one protein in the class C tethering complex, and increasing aflatoxin synthesis and export |
|
| DCC4849 | Spam (signal Peptide-based Affinity Maturated Ligand) | Novel Programmed Death Ligand 1 (PD-L1) Binding Peptide (a Peptide Ligand for PD-L1) |
|
| DCC4850 | spb03924 | Novel telomerase inhibitor |
|
| DCC4851 | SPB08007 | 0 |
|
| DCC4852 | Spd-2-am | Novel photo-controllable hydrogen sulfide donor applicable in live cells |
|
| DCC4853 | Spectinamide-1599 | Novel anti-tuberculosis agent against intracellular Mycobacterium tuberculosis |
|
| 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 |
|
| DCC4855 | Spi-1865 | Novel gamma-secretase modulator |
|
| DCC4856 | Spirohydantoin-21 | Novel selective orally bioavailable inhibitor of p300/CBP histone acetyltransferase |
|
| DCC4857 | Spirooxindole 1a | Novel p53 Stabilizer for Brain Cell Differentiation |
|
| DCC4858 | Spiroxamine | Sterol Biosynthesis Inhibitor, Fungicide |
|
| DCC4859 | Spla2 Inhibitor Pyr-1 | Novel potent sPLA2 inhibitor, selectively targeting hGIIA and hGIID |
|
| DCC4860 | Spmtrien | Novel isosteric charge-deficient spermine analogue |
|
| DCC4861 | spongiacidin C | USP7 inhibitor from the marine sponge Stylissa massa |
|
| DCC4862 | Spongosine | Pivotal intercellular signal transmitter |
|
| DCC4863 | Spop-in-6lc | Novel SPOP inhibitor, suppressing the viability and inhibiting the colony formation of ccRCC cell lines driven by cytoplasmic SPOP |
|
| DCC4864 | Spt-in-1 | Novel potent serine palmitoyl transferase (SPT) inhibitor |
|
| DCC4865 | Sptssb-binder-18 | Novel potent and selective binder of small subunit B of the serine palmitoyltransferase complex (SPTSSB) |
|
| 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 |
|
| DCC4867 | Sr-01000634273-1 | Novel inhibitor of the in vivo aggregation of |
|
| DCC4868 | Sr10098 | Novel NR4A nuclear receptor modulator |
|
| DCC4869 | Sr10658 | Novel NR4A nuclear receptor modulator |
|
| DCC4870 | Sr142948a | Selective neurotensin antagonist |
|
| DCC4871 | Sr-17398 Hydrochloride | Novel Unc-51-Like Kinase 1 (ULK1) |
|
| DCC4872 | Sr2067 | Novel partial agonist of PPARgamma |
|
| DCC4873 | Sr24237 | Novel NR4A nuclear receptor modulator |
|
| DCC4874 | Sr-3737 | Potent inhibitor of both JNK3 and p38 |
|
| DCC4875 | Sr-4326 | Novel Inhibitor of c-Jun N-terminal Kinase 3 (JNK3) |
|
| DCC4876 | Sr-43845 | Novel renin inhibitor |
|
| DCC4877 | Sr-58611a | The first selective β3 adrenergic agonist, showing to possess a profile of antidepressant activity in rodents |
|
