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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC4367 | Rad35010 |
Novel potent selective androgen receptor modulator (SARM)
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| DCC4366 | Rac-tofacitinib |
Inhibitor of Janus kinases
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| DCC4364 | Rachelmycin |
Novel potent DNA-alkylating agent, inhibiting TBP/DNA interaction
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| DCC4363 | Racemetirosine Methyl Ester Hcl |
Prodrug of Racemetirosine, an inhibitor of tyrosine 3-monooxygenase
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| DCC4362 | Rac-azd8186 |
Novel inhibitor of PI3Kβ and PI3Kδ, inhibiting growth of PTEN deficient breast and prostate tumor
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| DCC4361 | R93274 |
Potent and selective antagonist of 5-HT2A receptors
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| DCC4360 | r78206 |
Efficient stabilizer of Mahoney procapsids
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| DCC4359 | R523062 |
Novel Antiviral agent for Enterovirus D68
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| DCC4358 | r-154716 |
Novel inhibitor of HDL uptake induced by overexpression of scavenger receptor BI (SR-BI)
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| DCC4357 | r-138329 |
Novel scavenger receptor class B type I blocker
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| DCC4356 | R(ccug) Ligand 63 |
Novel Potent and Specific Ligand of r(CCUG)exp, Targeting r(CCUG) Repeats in Myotonic Dystrophy Type 2, Facilitating Degradation by RNA Quality Control Pathways
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| DCC4355 | R-(+)-eu-1180-453 |
Second-Generation GluN2C- and GluN2D-selective positive allosteric modulator (PAM) of the N-methyl-d-aspartate (NMDA) receptor
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| DCC4354 | Qw-296 |
Novel microtubule destabilizer
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| DCC4353 | Quoromycin |
Novel antivirulence agent against Vibrio vulnificus, inhibiting the quorum-sensing signaling pathway by controlling the DNA-binding affinity of SmcR and thus effectively alleviating the virulence of V. vulnificus in vitro and in vivo
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| DCC4352 | Quinine Sulfate |
Natural disrupter of DNA replication and transcription via DNA intercalation, reducing oxygen intake and carbohydrate metabolism and the excitability of muscle fibers, inhibiting the drug efflux pump P-glycoprotein
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| DCC4351 | Quilseconazole Besylate |
Potent, orally active fungal Cyp51 (lanosterol 14-α-demethylase) inhibitor
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| DCC4350 | Quazepam |
Modulator of specific GABAA receptors via the benzodiazepine site on the GABAA receptor
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| DCC4349 | Quatcy-i2 |
Novel photodynamic antitumor agent
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| DCC4348 | Qtc-4-meobne |
Novel multitarget anti-AD agent, significantly increasing in adult neurogenesis and remyelination through Prox1/NeuroD1 and Wnt/β-catenin pathways, demonstrating beneficial effects in preclinical models of AD
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| DCC4347 | Qs Inhibitor 2 |
Novel potent inhibitor of quorum sensing (QS) pathways, strongly blocking agr-type QS in S. aureus
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| DCC4346 | Qs Inhibitor 1 |
Novel potent inhibitor of quorum sensing (QS) pathways, strongly blocking agr-type QS in S. aureus
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| DCC4345 | Qndesa |
Novel fluorescent molecular rotor for the selective detection of the hybrid-conformation 22AG G-Quadruplex
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| DCC4344 | Qls-81 |
Novel Nav1.7 channel blocker (IC 50 at 3.5±1.5 μM). being efficacious on chronic pain in mice
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| DCC4343 | Qd394-me |
Novel reactive oxygen species (ROS) inducer, showing significant cytotoxicity in pancreatic cancer cells
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| DCC4342 | Qc-308 Hydrochloride |
Novel Heme Oxygenase-1 Inhibitor (HO-1 IC 50 =0.27μM; HO-2 IC 50 =0.46μM)
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| DCC4341 | q94 Hydrochloride |
Selective PAR1 negative allosteric modulator
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| DCC4340 | Q8pnap |
Novel class of bright near infrared window II (NIR-II, 1,000 - 1,700 nm) probe, being successfully used to achieve high spatial and temporal resolution imaging of hind limb vasculature, lymphatic system, and small tumor metastasis, as well as precise NIR-
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| DCC4339 | Pz-1444 |
Novel inverse agonist of 5-HT6 receptor
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| DCC4338 | Pyy3-36 |
Y2/Y5 Neuropeptide Y receptor agonist, reducing food intake in normal-weight and obese individuals and the plasma levels of the hunger-promoting hormone ghrelin
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| DCC4337 | Pysoca Substrate-1 |
Novel BBB-permeable substrate of pyrilamine-sensitive proton-coupled organic cation antiporter (PYSOCA), acting as a selective class I HDAC inhibitor
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