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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4509 | Rtiox-372 |
Novel Potent and Selective Orexin-1 Receptor Antagonist
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| DCC4508 | Rti-97 |
Novel potent and selective KOR antagonist
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| DCC4507 | Rti-371 |
Selective inhibitor of the dopamine transporter (DAT), blocking cocaine-induced locomotor stimulation and acting as a positive allosteric modulator of the human CB1 (hCB1) receptor
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| DCC4506 | Rta-1701 |
Novel allosteric RORγt inverse agonist
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| DCC4505 | rsva314 |
Potent indirect activator of AMPK
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| DCC4504 | Rsr-056 |
Specific ligand to CB2-positive spleen tissue of rats and mice
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| DCC4503 | Rs-8359 |
Selective and reversible Monoamine_oxidase_A>monoamine oxidase A (MAO-A) inhibitor
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| DCC4501 | Rs23597-190 Hydrochloride |
Potent and selective competitive antagonist of 5-HT4 receptors
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| DCC4500 | Rs-104966 |
Selective collagenase inhibitor, inducing the conformational change in the side-chains of the S1 pocket of MMP-1
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| DCC4499 | Rs-0466 |
Novel inhibitor of β-amyloid-induced cytotoxicity
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| DCC4498 | Rpw-24 |
Novel stimulator of host immune defenses, Inducing the transcription of putative immune effectors in C. elegans
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| DCC4497 | Rp-3-161 |
Novel stimulator of autophagy, inhibiting Mycobacterium tuberculosis survival in macrophages, and targeting Pik1
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| DCC4496 | Rp-23618 |
Novel non-peptidic RANTES antagonist
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| DCC4495 | Rp-001 Hydrochloride |
Potent agonist of S1P1 receptors
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| DCC4494 | Roxatidine Acetate |
Specific and competitive H2 receptor antagonist
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| DCC4493 | Rovafovir Etalafenamide |
Prodrug of the novel nucleoside phosphonate HIV reverse transcriptase (RT) inhibitor GS-9148
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| DCC4492 | Rovafovir |
Novel nucleoside phosphonate HIV reverse transcriptase (RT) inhibitor
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| DCC4491 | Rostaporfin |
Photosensitiser for the treatment of age-related macular degeneration
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| DCC4490 | Ros-modulator-3b |
Novel P2X3 antagonist
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| DCC4489 | Rosma-18-d6 |
Novel potent and selective CB2 probe (Ki for CB2: 0.8 nM and >12000 selectivity over CB1)
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| DCC4488 | Rorγt-inverse-agonist-1j |
Novel potent RORγt inverse agonist
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| DCC4487 | Rorγt Agonist |
Novel RORγt agonist
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| DCC4486 | Rorgammat Inhibitor I |
Novel RORgammaT inhibitor
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| DCC4485 | Rorgammat Agonist 8-074 |
Novel potent and selective RORγt agonist, showing robust antitumor efficacy in syngeneic tumor models and improving the efficacy of anti‑PD‑1 in a murine lung cancer model
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| DCC4484 | Ror Modulator I |
The first potent inverse agonist of retinoid-related orphan receptor (ROR) with dual selectivity for RORβ and RORγt
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| DCC4483 | Ropizine |
Allosteric modulator of dextromethorphan binding to high-affinity sigma receptors
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| DCC4482 | Rooperol |
Novel p38α kinase inhibitor; Antioxidant
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| DCC4481 | Ronifibrate |
Lipid modifying agent; Antihyperlipidemic and antiarteriosclerotic
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| DCC4480 | Rohitukine |
Anti-cancer agent, acting through gastrin antagonism and H /K -ATPase inhibition, modulating apoptosis pathways, antidyslipidemic, antiadipogenic, gastroprotective, antifertility, and antileishmanial
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| DCC4479 | Rock-in-d3 |
Novel potent and selective ROCK inhibitor
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