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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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