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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4686 | Sertaconazole |
Cytochrome P450 14α-demethylase inhibitor, also acting as a BuChE-IDO1 inhibitor
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| DCC4685 | Sert Inhibitor 69419 |
Novel serotonin reuptake inhibitor
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| DCC4684 | Ser@tpp@cur |
Novel mitochondrial KIM-1 receptor modulator to be specifically internalized by renal tubular epithelial cells via KIM-1 receptor-mediated endocytosis and then actively distributed in mitochondria under the effect of TPP, effectively ameliorating injured
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| DCC4683 | Sephin1 Hydrochloride |
Selective inhibitor of the phosphatase regulatory subunit PPP1R15A (R15A) that prolong the benefit of eIF2α phosphorylation, thereby protecting cells from proteostatic defects
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| DCC4682 | Se-nsaid-8 |
Novel selenium-nonsteroidal anti-inflammatory drug (Se-NSAID), inhibiting colorectal cancer (CRC) growth via the inhibition of the cell cycle in G1 and G2/M phases and reduces the cell cycle markers like cyclin E1 and B1 in a dose dependent manner
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| DCC4681 | Senp1-in-8e |
Sentrin-specific protease 1 (SENP1) inhibitor
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| DCC4680 | Sen-826 |
Novel potent antagonist of the Hedgehog pathway
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| DCC4679 | Sen461 |
Novel Wnt inhibitor/Axin stabilizer
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| DCC4678 | Sen205a |
Novel S100B inhibitor
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| DCC4677 | Sempai |
Novel AkaLumine analog, acting asa NIR emission luciferin with the enhanced solubility in water
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| DCC4676 | Seh-in-12 |
Novel potent inhibitor of the enzyme soluble epoxide hydrolase (sEH)
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| DCC4675 | Seh/ache Inhibitor 12c |
Novel Highly Potent Dual Inhibitor of Soluble Epoxide Hydrolase and Acetylcholinesterase for the Treatment of Alzheimer's Disease
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| DCC4674 | Securinine Mononitrate |
Antagonist of gamma-aminobutyric acid A (GABA A ) receptor and cholinergic agent
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| DCC4673 | Seco-rapamycin Ethyl Ester |
Novel open-ring metabolite of rapamycin derivative
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| DCC4672 | Secologanate |
Natural plant growth inhibitor
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| DCC4671 | sdz-nkt343 |
Highly selective human tachykinin NK1 receptor antagonist
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| DCC4670 | Sdz-lap-977 |
Potent antiproliferative agent, binding to the “colchicine binding site” on tubulin and inhibiting tubulin polymerization in vitro
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| DCC4669 | sdz-285604 |
Novel inhibitor of sterol 14a-demethylases (CYP51)
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| DCC4668 | Sdz Ser 082 Fumarate |
Selective 5-HT2B/2C receptor antagonist
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| DCC4667 | Sdz Mrl 953 |
Novel immunostimulatory monosaccharidic lipid A analog, down-regulating TNF-alpha and IL-6 production and priming secretion of G-CSF and IL-1 beta
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| DCC4666 | Sdz 90-215 |
Novel inhibitor of the Golgi complex (Vrg4); Antifungal
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| DCC4665 | Sdz 205-557 Hydrochloride |
Selective, surmountable antagonist for 5-HT4 receptors
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| DCC4664 | Sd2590 Hydrochloride |
Potent inhibitor of MMP-2, -3, -9, -8, -13, and -14
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| DCC4663 | S-cw3554 |
Novel irriversible selective PDI inhibitor, selectively labeling protein disulfide isomerase and inhibiting its enzymatic activity, showing unique cytotoxicity in cells derived from multiple myeloma
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| DCC4662 | Scriptene |
NRTI-drug pair of zidovudine (AZT)-didanosine (ddI), being highly cytotoxic and mutagenic
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| DCC4661 | Scr-4026 |
Novel inhibitor of nNOS-PSD-95 interaction, exhibiting neuroprotective activities in NMDA-induced or Oxygen and glucose deprivation (OGD)-induced neuronal damage in primary cortical neurons cultures, and ameliorating focal cerebral ischemic damage in rats
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| DCC4660 | Scr1693 |
Novel dual acetylcholinesterase inhibitor (AChEI) and a calcium channel blocker (CCB)
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| DCC4659 | Scq-14d |
Novel Inhibitor of p53-Murine Double Minute 2 (MDM2) Interaction and Histone Deacetylases (HDACs) with the IC50 values of 140, 910 and 17.5 nmol/L against MDM2, HDAC1, and HDAC6, respectively, showing the tumor growth inhibition (TGI) in the A549 xenograf
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| DCC4658 | scio-469 Hydrochloride |
Selective, ATP-competitive p38
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| DCC4657 | Schembl20148701 |
Novel inhibitor of SARS-CoV-2 main protease (MPro)
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