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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4988 | Syk-524 |
Novel universal opioid receptor agonist
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| DCC4987 | Sy-5609 |
Novel highly potent and selective CDK7 inhibitor, demonstrating broad anti-tumor activity in vivo
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| DCC4986 | S-y048 |
Novel selective OXE receptor antagonist
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| DCC4985 | swertisin |
Potent differentiating agent
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| DCC4984 | Swainsonine |
Natural potent alpha-mannosidase inhibitor, exhibiting antimetastatic, antiproliferative, and immunomodulatory activities
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| DCC4983 | Sw208108 |
Novel clickable tumor-specific irreversible inhibitor of stearoyl CoA desaturase (SCD)
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| DCC4982 | Sv-iii-130s |
D2 dopamine receptor partial agonist in adenylyl cyclase inhibition assay and antagonist in the GIRK and phospho ERK1/2 assays
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| DCC4981 | Sv-293 |
Selective D2 dopamine receptor antagonist
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| DCC4980 | suvanine |
Antagonist of the mammalian bile acid sensor farnesoid-X-receptor (FXR)
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| DCC4979 | Supradamal |
Potent Inhibitor of Plasmodium FK506 Binding Protein 35 (FKBD35), also act as a HIV inhibitor
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| DCC4978 | Sun-c5174 |
5-HT2 antagonist
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| DCC4977 | Sun13837 |
Novel fibroblast growth factor receptor modulator for treating neurodegenerative diseases
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| DCC4976 | Sumanirole |
D2 selective dopamine agonist, showing anxiolytic and anti-parkinsonian activities
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| DCC4975 | Sulukast |
Novel, potent, selective, and competitive antagonist of LTD4 and LTE4
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| DCC4974 | Suloctidil Hydrochloride |
Peripheral vasodilator
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| 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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