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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4478 | Rock-in-d2 |
Novel potent and selective ROCK inhibitor
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| DCC4477 | Rock-in-d1 |
Novel potent and selective ROCK inhibitor
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| DCC4476 | Rock-in-32 |
Potent Rho--kinase (ROCK) inhibitor
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| DCC4475 | Rock-in-(r)14f |
Novel potent ROCK inhibitor
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| DCC4474 | Rockii-in-di |
Novel potent competitive inhibitor of Rho-associated coiled-coil-containing protein kinase 2 (ROCKII)
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| DCC4473 | Rocepafant |
Platelet-activating factor (PAF-R) antagonist, selectively for intracellular PAF binding sites
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| DCC4472 | Robalzotan |
Selective antagonist at the 5-HT1A receptor
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| DCC4471 | Ro7101556 |
Novel potent γ-secretase modulator (GSM) with high solubility, balanced lipophilicity, and showing no phototoxicity and PIK4CB side bing activity
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| DCC4470 | Ro6842262 |
Novel potent and selectve LPA1 antagonist, attenuating NHLF human lung fibroblast cell proliferation and contraction in vitro, reducing plasma histamine levels in mouse LPA-challenge model
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| DCC4469 | Ro6800020 |
Potent γ-secretase modulator (GSM)
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| DCC4468 | Ro-57-bpyne |
Novel γ-secretase modulator photoaffinity probe, identifying distinct allosteric binding sites on presenilin that can be exploited to reduce levels of pathogenic Aβ species
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| DCC4467 | Ro5527239 |
Novel potent, orally available GPBAR1 agonist
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| DCC4466 | Ro5234444 |
Orally active chemokine receptor CCR2 antagonist preventing glomerulosclerosis and renal failure in type 2 diabetes
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| DCC4465 | Ro4597014 |
Novel Glucokinase Activator for the Treatment of Type 2 Diabetes
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| DCC4464 | Ro4583298 |
Novel highly potent dual NK1/NK3 receptor antagonist
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| DCC4463 | Ro4491533 |
Selective negative allosteric modulator of mGlu3
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| DCC4462 | Ro4432717 |
Novel mGlu2/3 negative allosteric modulator (NAM)
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| DCC4461 | Ro-363 |
Beta(1) adrenoceptor-selective agonist
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| DCC4460 | ro3206145 |
Potent and selective inhibitor of the p38 MAPK catalytic domain
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| DCC4459 | Ro31-4724 |
Dual inhibitor of HDAC and MMP
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| DCC4458 | Ro26-4550 Tfa Salt |
Novel reversible inhibitor of interleukin-2 (IL-2)
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| DCC4457 | Ro-23-7553 |
Vitamin D analogue, showing significant in vitro and in vivo antitumor activity.
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| DCC4456 | Ro-09-4879 |
Potent and selective Candida albicans N-myristoyltransferase (CaNmt) inhibitor, exhibiting antifungal activity in vivo
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| DCC4455 | Ro-09-4609 |
Potent and selective Candida albicans N-myristoyltransferase (CaNmt) inhibitor
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| DCC4454 | Ro 8-4304 Hydrochloride |
NMDA receptor antagonist , specifically suppressing the severe autoimmune phenotypes of chs3-2D (chilling sensitive 3, 2D), including the arrested growth morphology and heightened PR (Pathogenesis Related) gene expression
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| 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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