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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC5219 | Trans-ocma |
Natural specific inhibitor of γ-secretase, decreasing amyloid-beta levels without influencing cleavage of Notch, showing strong growth inhibitory effects on cancer cell lines and significant anti-complement activity, also acting as a PTP1B inhibitor
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| DCC5218 | Trans-miyabenol C |
Natural resveratrol trimer, acting as a protein kinase C inhibitor
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| DCC5217 | Trans-cbtbp |
Novel KGA allosteric inhibitor
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| DCC5216 | Trans-bopc1 |
Novel HuR binder, modulating HuR-RNA interactions
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| DCC5215 | Trans-abcd |
Potent and selective NMDA agonist
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| DCC5214 | Trans- Resveratrol-4’-sulfate Sodium Salt |
Metabolite of Resveratrol
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| DCC5213 | Tracizoline |
Potent I 2 -imidazoline receptor agonist
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| DCC5212 | Tp-s1-68 |
Novel Type-I Inhibitor of TIE-2
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| DCC5211 | Tpp-cl2 |
Mitochondria-activatable luciferin (MAL-Probe)
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| DCC5210 | Tpmp-i-2 |
Enhancer of the cytotoxic effect of immunotoxins (ITs) which results in increased apoptosis in different cancer cells
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| DCC5209 | Tpl2-in-i |
Novel tumour progression locus 2 (Tpl2) kinase inhibitor
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| DCC5208 | Tpi-287 |
Novel taxane family member, reducing the brain metastatic colonization of breast cancer cells
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| DCC5207 | Tpi-2659-17 |
Novel Specific Inhibitor of Type I Collagen Production in Fibrosis
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| DCC5206 | Tpi-1917-49 |
Promising amyloid reducing agent by lowering the levels of Aβ.
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| DCC5205 | Tpi1609-10 |
Inhibitor of tyrosine recombinases and Holliday junction-resolving enzymes; Antibacterial
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| DCC5204 | Tph1-in-23a |
Novel Peripheral Selective Tryptophan Hydroxylase 1 (TPH1) Inhibitor (IC 50 : 42nM) for Obesity and Fatty Liver Disease
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| DCC5203 | Tpe-gal |
First-in-class fluorescent drug delivery vesicle that can efficiently load both water-soluble and -insoluble anticancer drugs
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| DCC5202 | Tp-238 Hydrochloride |
Novel probe for CECR2/BPTF bromodomains
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| DCC5201 | Tp-040 |
Novel inhibitor of O-GlcNAcase (OGA)
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| DCC5200 | Tp-008 |
Novel probe for activin receptor-like kinase (ALK4 and ALK5)
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| DCC5199 | Toxt-in-8 |
Novel ToxT inhibitor, reducing Vibrio cholerae virulence in vivo and effectively inhibiting intestinal colonization in the infant mouse
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| DCC5198 | Tosylaniline |
Selective CA IX inhibitor
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| DCC5197 | Tos-gly-pro-arg-anba-ipa |
Chromogenic peptide substrate for the rapid and specific photometric assay of recombinant hirudin (r-hirudin)
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| DCC5196 | Tortuosamine |
Natural psychoactive agent
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| DCC5195 | To-pro3 Iodide |
Nucleic acid stain, acting on viable, early apoptotic and necrotic cells differentially, showing specific staining of nuclei without any staining of the cytoplasm
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| DCC5194 | Topki-nbd |
Novel highly specific fluorescent TOPK inhibitor
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| DCC5193 | Top-dnj |
Novel Selective Inhibitor of Endoplasmic Reticulum α-Glucosidase II, Exhibiting Antiflaviviral Activity
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| DCC5192 | Top1210 |
Novel narrow spectrum kinase inhibitor, potently inhibiting P38a, Src, and Syk kinase activities
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| DCC5191 | Top1/tdp1-in-c12 |
Novel dual TOP1 and TDP1 inhibitor, inducing both cellular TOP1cc, TDP1cc formation and DNA damage, resulting in cancer cell apoptosis at a sub-micromolar concentration
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| DCC5190 | Tonantzitlolone |
Natural agonist of TPRC1/4/5 channels, also acting as a dual PKCα and PKCθ activator, inducing an insulin resistant phenotype by inhibiting IRS1 and the PI3K/Akt pathway, activating the heat shock factor 1 (HSF1) transcription factor driving glucose depen
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