| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC9584 | (R)-(-)-Rolipram | (R)-(-)-Rolipram is a potent and cAMP-specific PDE4 inhibitor with IC50 of 0.22 uM; 2.5-fold more potent than (+)-rolipram (IC50= 2.58 uM) in inhibiting membrane-bound PDE 4. |
|
| DC11910 | IPL-576092 | A novel orally active, anti-inflammatory compound that inhibits leukocyte infiltration and changes in lung function in response to allergen challenge. |
|
| DC11802 | AX-024 free base Featured | AX-024 is an cytokine release inhibitor which can strongly inhibit the production of interleukin-6 (IL-6), tumor necrosis factor-α (TNFα), interferon-γ (IFN-γ), IL-10 and IL-17A. |
|
| DC10545 | AX-024 HCl Featured | AX-024 is the first-in-class inhibitor of T cell receptor (TCR); AX-024 is an orally available inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation (IC50 value 1 nM). |
|
| DC10724 | AZD2098 Featured | AZD2098 is a potent CC-chemokine receptor 4 (CCR4) inhibitor, used for asthma research. |
|
| DC9117 | Bambuterol HCl | Bambuterol Hcl is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a prodrug of terbutaline. |
|
| DC11278 | Fevipiprant Featured | Fevipiprant(QAW039) is a selective, potent, reversible competitive CRTh2 antagonist with an in vitro dissociation constant KD value of 1.1nM at the CRTh2 receptor and an IC50 value of 0.44 nM for inhibition of PGD2-induced eosinophil shape change. |
|
| DC10721 | Gefapixant(AF-219,MK-7264) Featured | Gefapixant(AF-219,MK-7264) is novel P2X3 receptor antagonist. |
|
| DC12342 | Gemilukast (ONO-6950) | Gemilukast is an orally active and potent dual cysteinyl leukotriene 1 and 2 receptors (CysLT1 and CysLT2) antagonist, with IC50s of 1.7, 25 nM for human CysLT1 and CysLT2, respectively. |
|
| DC7837 | GW-3965 hydrochloride Featured | GW3965 HCl is a potent, selective LXR agonist for hLXRα and hLXRβ with EC50 of 190 and 30 nM, respectively. |
|
| DCAPI1208 | L-NAME HCl | L-NAME is a nonselective inhibitor of nitric oxide synthetases (NOS) for nNOS (bovine), eNOS (human), and iNOS (murine), with Ki of 15 nM, 39 nM and 4.4 μM, respectively. |
|
| DC9279 | MK-571 Featured | MK-571 is a selective, orally active CysLT1 receptor antagonist. |
|
| DC9448 | MK591 | MK591(Quiflapon sodium) is a selective and specific 5-Lipoxygenase-activating protein (FLAP) inhibitor. |
|
| DC7471 | N6022 Featured | N6022 is a potent, selective, reversible, and efficacious S-Nitrosoglutathione reductase(GSNOR) inhibitor(IC50=10 nM) which is currently undergoing clinical development. |
|
| DC9583 | Oglemilast Featured | Oglemilast(GRC3886) is a potent PDE4 inhibitor, under clinical studies in the treatment of allergen-induced asthma. |
|
| DC11671 | RPL-554 | RPL-554 (LS-193855, RPL554) is a potent, orally available, dual PDE3/PDE4 inhibitor with IC50 of 0.4 nM and 1479 nM, respectively. |
|
| DC8436 | Salmeterol Xinafoate Featured | Salmeterol Xinafoate is a long-acting β2-adrenergic receptor agonist with anti-inflammatory effects, used in the treatment of asthma symptoms and chronic obstructive pulmonary disease (COPD) symptoms. |
|
| DC7777 | Valategrast (R411) | Valategrast (R411), a small molecule antagonist of α4β1 integrin, represents a potential therapy for asthma |
|
| DCAPI1015 | Zafirlukast(Accolate) | Zafirlukast(Accolate) |
|
