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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4973 | Sulfosuccinimidyl Oleate Sodium |
Neuroprotective agent, alleviating stroke-induced neuroinflammation
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| DCC4972 | Sulfonyl Quinoxaline 1 |
Novel inhibitor of RhoG-hepcidin uptake
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| DCC4971 | Sulfazecin |
β-Lactam antibiotic against multi-drug resistant pathogens
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| DCC4970 | Sulfacetamide |
Antibacterial, inhibiting bacterial folic acid synthesis by competing with para amino benzoic acid
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| DCC4969 | Sul-121 Hydrochloride |
Novel inhibitor of airway inflammation and hyperresponsiveness in experimental models of chronic obstructive pulmonary disease (COPD)
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| DCC4968 | Suku-33 |
Novel potent inhibitor of osteoclastogenesis, suppressing both equilibrative nucleoside transporters and concentrative nucleoside transporters
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| DCC4966 | Suc-leu-leu-val-tyr-amc |
Fluorescent substrate which can be hydrolyzed by the proteasome to release free AMC and the fluorescence of which is proportional to the proteasome activity
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| DCC4965 | Subglutinol A |
Natural immunosuppressive agent, effectively blocking T cell proliferation and survival while profoundly inhibiting pro-inflammatory IFNγ and IL-17 production by fully differentiated effector Th1 and Th17 cells, also acting as an estrogen receptor antagon
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| DCC4964 | Su9518 |
Novel potent and selective inhibitor of the cellular PDGF receptor kinase and PDGF receptor-induced cell proliferation
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| DCC4963 | Su-200 |
Agonist of TRPV1
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| DCC4962 | Su11652 |
Sunitinib analog, acting as a potential inhibitor for nucleoside diphosphate kinase (NDK) from Leishmania major (LmNDK)
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| DCC4961 | Su11606 |
Potent c-MET inhibitor
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| DCC4960 | Su11272 |
Novel potent c-MET inhibitor
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| DCC4959 | Su0383 |
Novel dual Inhibitor of repair enzymes 8-oxoguanine DNA glycosylase (OGG1) and human MutT Homolog 1 (NUDT1 or MTH1), increasing sensitivity of tumor cells to oxidative stress
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| DCC4958 | Stx2845 |
Novel Nonsteroidal Inhibitor of Carbonic Anhydrase IX
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| DCC4957 | Stx-2622 |
Inhibitor of 17β-hydroxysteroid dehydrogenases (17β-HSDs)
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| DCC4956 | Sts-e424 |
Novel agonist of the tissue-protective erythropoietin (EPO) receptor, increasing FXN expression and EPOR phosphorylation
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| DCC4955 | Sts-e412 |
The first nonpeptidyl, selective activator of the tissue-protective EPOR/CD131 receptor
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| DCC4954 | Streptozocin |
Antibiotic, being used as an antineoplastic agent and to induce diabetes in experimental animals
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| DCC4953 | Streptolidine |
Metablite of the Streptomyces antibiotics streptothricin and streptolin
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| DCC4952 | Stock1n-65837 |
Potent natural modulator of human Toll-like receptor 7 (TLR7)
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| DCC4951 | Stk683963 |
Novel activator of cellular ATG4B activity
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| DCC4950 | Stk630921 |
Novel blocker of IL-17A binding to the IL-17A receptor (IL-17RA)
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| DCC4949 | Stk508411 |
Novel inhibitor of the heterogeneous ribonuclear protein A18 (hnRNP A18)
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| DCC4948 | Stk295900 |
Dual inhibitor of topoisomerase 1 and 2, inducing G(2) arrest in the absence of DNA damage. Inhibitor of Plasmodium falciparum W2 (drug-resistant) proliferation in erythrocyte-based infection assay
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| DCC4947 | Stk-22 |
Novel Fatty Acid Binding Protein 5 (FABP5) Inhibitor
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| DCC4946 | Stk-15 |
Novel Fatty Acid Binding Protein 5 (FABP5) Inhibitor
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| DCC4945 | Sting Inhibitor C-171 |
Novel covalent antagonist of hsSTING
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| DCC4944 | Sting Agonist 11 |
Novel non-nucleotide STING agonist, demonstrating antitumor activity when dosed intratumorally in a syngeneic mouse model
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| DCC4943 | Stictic Acid |
Natural anti-feline infectious peritonitis virus (FIPV) agent, specifically targeting the 3CLpro of FIPV and inhibiting its replication
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