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Cat. No. Product Name Field of Application Chemical Structure
DCC4453 Ro 8-4304
Novel NR2B selective, non-competitive, voltage-independent antagonist
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DCC4452 Ro 64-5229
Selective, non-competitive Metabotropic_glutamate_receptor>mGlu2 antagonist
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DCC4451 Ro 48-8587
Competitive AMPA receptor antagonist
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DCC4450 Ro 32-7315
ADAM17-selective inhibitor
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DCC4449 Ro 31-8220
Potent protein kinase C (PKC) inhibitor
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DCC4448 Ro 25-6981 Benzoate
Potent and selective antagonist of NMDA glutamate receptors containing the NR2B subunit
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DCC4447 ro 115-1240
Selective alpha1A/1L-adrenoceptor partial agonist
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DCC4446 Ro 04-5595 Hydrochloride
Selective antagonist of NMDA receptors NR2B subunits
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DCC4445 Rna Ligand Tppc
Novel potent and specific RNA-binding ligand, targeting riboswitches and other RNAs at proximal subsites
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DCC4444 rn-450
Potent, reversible, non-carbonyl inhibitor of fatty acid amide hydrolase (FAAH)
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DCC4443 Rms-07
The first irreversible covalent MPS1 inhibitor, targeting a poorly conserved cysteine in the kinase's hinge region
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DCC4442 Rm-581-fluo
Novel Fluorescent ER-Tracker dye, showing potent cytotoxic activity on several types of cancer cells, being accumulated into the endoplasmic reticulum (ER) as highlighted by its colocalization
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DCC4441 Rm1490
Novel MOR agonist
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DCC4440 Rm-133
Promising pro-apoptotic agent, showing activity on various cancer cell lines
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DCC4439 Rm-131
Novel gastrocolokinetic ghrelin agonist, approximately sixfold greater potency than natural ghrelin
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DCC4438 Rl-338
Novel potent and highly selective GPR6 inverse agonist, inhibiting GPR6 cAMP signalling in TR-FRET assays with a EC50 = 16 nM and >100 fold selectivity against GPR3 and GPR12
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DCC4437 Rkn5755
Novel selective inhibitor of activated fibroblasts, inhibiting the enhanced migration of fibroblasts cocultured with cancer cells by binding to β-arrestin1 and interfering with β-arrestin1-mediated cofilin signaling pathways
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DCC4436 Rk-9123016
Novel potent and selective SIRT2 inhibitor, increasing the acetylation level of eukaryotic translation initiation factor 5A (eIF5A) and reducing cell viability of human breast cancer cells accompanied with a decrease in c-Myc expression
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DCC4435 Rk-682
Natural selective inhibitor of protein tyrosine phosphatases (PTPases)
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DCC4434 Rk-0404678
Novel inhibitor of dengue virus NS5 RNA-dependent RNA polymerase (RdRp), inhibiting the DENV type 2 (DENV2) RdRp activities
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DCC4433 Rjw100
Novel potent Liver Receptor Homolog-1 (LRH-1) modulator
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DCC4432 Rjr-2403 Fumarate
Highly selective α4β2 subtype nicotinic receptor agonist
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DCC4431 Rivoglitazone Hydrochloride
Novel peroxisome proliferator-activated receptor gamma (PPARgamma) agonist
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DCC4430 Ripk2 Protac 20
Novel IAP-based selective RIPK2 degrader
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DCC4429 Rip2-in-3
First-in-Class Receptor Interacting Protein 2 (RIP2) Kinase Specific inhibitor
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DCC4428 Rinoxiab
Natural inducer of apoptosis by significantly upregulating Bcl-2, mitigating expression of Bcl2 in HCT 15 cells and attenuating the apoptotic markers and cell cycle regulatory proteins
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DCC4427 R-imeglimin
Novel antidiabetic agent, impairing glucose uptake by muscle tissue, excessing hepatic gluconeogenesis, and increasing beta-cell apoptosis
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DCC4426 Rilpivirine Hydrochloride
HIV-1 reverse transcriptase inhibitor, also acting as an EC 2.7.7.49 (RNA-directed DNA polymerase) inhibitor
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DCC4424 Rifamycin Sv
Natural antibiotic, inhibiting prokaryotic DNA-dependent RNA synthesis and protein synthesis; blocking RNA-polymerase transcription initiation, modulating ß2m aggregation
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DCC4423 Rifametane
Antibiotic for tuberculosis (TB) treatment
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