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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4407 | Rg7388-tco |
Highly Potent Clickable Probe for Cellular Imaging of MDM2 and Assessing Dynamic Responses to MDM2-p53 Inhibition
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| DCC4406 | Rg-102240 |
Gene switch ligand as a transcription inducer for use in induceable gene expression systems
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| DCC4405 | Rf470dl |
Novel fluorescent D-amino acid for labeling peptidoglycans (PG) in live bacteria
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| DCC4404 | Rf3286 |
Novel Highly Selective Neuropeptide FF1 Receptor Antagonist, Potently Preventing Opioid-Induced Hyperalgesia
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| DCC4403 | Rf04289 |
Novel TLR2 activator
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| DCC4402 | Reveromycins Inducer Br-1 |
Novel biomediator that induces reveromycins production at the wide range of concentrations without affecting cell growth
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| DCC4401 | Revamilast |
Novel phosphodiesterase IV (PDE4) inhibitor for the treatment of Asthma and Rheumatoid Arthritis
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| DCC4400 | Rev1/ubm2 Inhibitor |
Novel inhibitor of the REV1/UbPCNA interaction, directly binding to REV1 UBM2 and preventing DNA damage tolerance (DDT)
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| DCC4399 | Retro-2.1 |
Novel potent inhibitor of EBOV infection and entry
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| DCC4398 | Resveratrol-4’-sulfate |
Metabolite of Resveratrol
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| DCC4397 | resveratrol-3-sulfate |
Metabolite of Resveratrol
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| DCC4396 | Resorufin-r1 |
Red-absorbing, water-soluble, and iodinated resorufin derivative, being selectively activated with a monoamine oxidase (MAO) enzyme, showing high 1O 2 generation yields in aqueous solutions upon addition of MAO isoforms
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| DCC4395 | Resorcinolnaphthalein |
Angiotensin-converting enzyme 2 (ACE2) activator, acting as a modulator on RAAS and KKS activation during COVID-19
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| DCC4394 | Resiniferatoxin |
Potent VR1 vanilloid receptor agonist, activating protein kinase C
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| DCC4393 | Resazurin |
Oxidation-reduction indicator in cell viability
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| DCC4392 | Repinotan Hydrochloride |
Selective 5-HT1A receptor agonist
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| DCC4391 | Rep8839 |
Novel bacterial methionyl t-RNA synthetase (MRS) inhibitor, hampering Plasmodium growth very effectively
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| DCC4390 | Renzapride Hydrochloride |
5-HT3 antagonist and 5-HT4 agonist, also acting as a 5-HT2B antagonist
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| DCC4389 | Remifentanil |
Potent ultra short-acting synthetic unique opioid analgesic
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| DCC4388 | Remeglurant |
Novel selective antagonist of the mGlu5 receptor
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| DCC4387 | regacin |
Novel specific inhibitor of the ability of RegA to activate its target promoters, reducing expression of a number of proteins required for virulence
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| DCC4386 | Redx04739 |
Novel inhibitor of the supercoiling and ATPase reactions of DNA gyrase, inhibiting gyrase by preventing the binding of ATP and showing selectivity against M. smegmatis.
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| DCC4385 | Redx03863 |
Novel potent inhibitor of the supercoiling and ATPase reactions of DNA gyrase, inhibiting gyrase by preventing the binding of ATP
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| DCC4384 | Redoxal |
Novel Prenyltransferase Inhibitor with In Vitro and In Vivo Antibacterial Activity
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| DCC4383 | Recql5-in-4a |
Novel potent inhibitor of RECQL5-helicase activity, and stabilizing RECQL5-RAD51 physical interaction, leading to impaired HRR and preferential killing of RECQL5-expressing breast cancer
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| DCC4382 | Rds-2197 |
Novel HIV-1 Integrase Inhibitor
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| DCC4381 | Rds-1997 |
Novel HIV-1 Integrase Inhibitor
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| DCC4380 | Rdrp Inhibitor 11q |
Novel Potent Broad-Spectrum Inhibitor of Influenza A Virus RNA-Dependent RNA Polymerase (RdRp)
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| DCC4379 | Rc-33 Hydrochloride |
Novel highly potent, selective, and metabolically stable σ1 receptor agonist potentiating NGF-induced neurite outgrowth
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| DCC4378 | Rbpi-3 |
Selective inhibitor of poly(ADP-Ribose) glycohydrolase (PARG)
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