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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4377 | Rbm2-1d |
Novel dual inhibitor of dihydroceramide desaturase (dhCerDS) and acid ceramidase (ACDase)
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| DCC4376 | Rbm2-1b |
Novel dual inhibitor of dihydroceramide desaturase (dhCerDS) and acid ceramidase (ACDase)
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| DCC4375 | R-bc154 |
Potent fluorescent α4β1/α9β1 inhibitor
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| DCC4374 | Raseglurant |
Novel metabotropic glutamate type 5 (mGlu5) receptor negative allosteric modulator (NAM)
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| DCC4373 | Ram2093 |
Novel inhibitor of geranylgeranyl diphosphate synthase (GGDPS)
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| DCC4372 | Ram2061 |
Novel inhibitor of geranylgeranyl diphosphate synthase (GGDPS), showing significant reduction in tumor growth in mice
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| DCC4371 | Ralimetinib |
Novel potent inhibitor of p38 MAPK
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| DCC4370 | Radotinib Dihydrochloride |
Novel inhibitor of the tyrosine kinase BCR-ABL and platelet-derived growth factor receptor, inhibiting mitosis entry in acute myeloid leukemia cells via suppression of Aurora kinase A expression
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| DCC4369 | Radicicol |
Hsp90 N-terminal inhibitor
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| DCC4368 | Radical Scavenger C7 |
Potent anti-free radical agent, elevating glutathione peroxidase (GSH-PX) and super oxide dismutase (SOD) levels and lowering malonaldehyde (MDA) level in vivo in the Alzheimer's model
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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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