| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC34279 | HOE-766 | Buserelin Acetate is a Gonadotropin-releasing hormone agonist (GnRH agonist). |
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| DC34280 | 2-MeS-ADP | 2-MeS-ADP is a purinergic agonist. It acts by displaying selectivity for P2Y1, P2Y12 and P2Y13 receptors and inhibiting cAMP accumulation. |
|
| DC34281 | 6-OHDA HBr | 6-OHDA HBr is a neurotoxin. It acts by destroying catecholaminergic terminals. |
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| DC34282 | AQ4 | AQ4 is a topoisomerase II inhibitor and DNA intercalator. |
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| DC34283 | Quinpirole dihydrochloride | Quinpirole dihydrochloride is a D2-like dopamine receptor agonist. |
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| DC34284 | (+)-Pinanediol | (+)-Pinanediol is an effective inducer of melanogenesis. It acts by inducing higher levels of pigmentation and synthesis of nitric oxide (NO) in S91 cells. |
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| DC34285 | GSNO | GSNO is an endogenous transnitrosation donor involved in S-nitrosation of a variety of cellular proteins. It acts by regulating diverse protein functions |
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| DC34286 | BRD6688 Featured | BRD6688 is a selective HDAC2 inhibitor. It acts by enhancing the learning and memory processes. |
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| DC34287 | Adenosine N1-oxide | Adenosine N1-oxide is an inhibitor of secretion of inflammatory mediators. It acts by suppressing pro-inflammatory cytokine secretion. |
|
| DC34288 | UCD38B HCl | UCD38B HCl is a cell permeable inhibitor of intracellular uPA (urokinase plasminogen activator). It acts by killing proliferative and non-proliferative high grade glioma cells by programmed necrosis. |
|
| DC34289 | NPY5RA972 Featured | NPY5RA972 is a neuropeptide Y Y5 antagonist. |
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| DC34290 | BAMF | BAMF is an acetylating agent for the chemical modification of proteins. |
|
| DC34291 | alphaSYN-IN-NAB2 | alphaSYN-IN-NAB2 is an inhibitor of α-synuclein mutations. It acts by reversing the α-synuclein-induced pathological phenotype in Parkinson's disease cortical neurons and promoting E3 ubiquitin ligase Rsp5/Nedd4-dependent endosomal transport.. |
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| DC34292 | 1,4-DPCA | 1,4-DPCA is a potent and selective inhibitor of prolyl 4-hydroxylase. |
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| DC34293 | 3-HIB | 3-HIB is a paracrine regulator of trans-endothelial fatty acid transport. |
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| DC34294 | Dexanabinol | Dexanabinol is a cannabinoid agonist. |
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| DC34295 | Wee1 Inhibitor I | Wee1 Inhibitor I is an ATP-binding site-targeting inhibitor of Wee1. |
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| DC34296 | FRJ | FRJ is a specific inhibitor of protein tyrosine phosphatase 1B (PTP1B). |
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| DC34297 | RA-2 | RA-2 is a pan-negative-gating modulator of KCa2/3 channels. It acts by inhibiting EDH-type relaxation in coronary arteries. |
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| DC34299 | TT01001 | TT01001 is a mitoNEET ligand. It acts by improving diabetes and ameliorates mitochondrial function in db/db mice. |
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| DC34300 | Fenoterol hydrobromide | Fenoterol is β2-Adrenergic receptor (β2-AR) agonist. Fenoterol is chemically closely related to metaproterenol (orciprenaline). It has a higher bronchodilating potency than metaproterenol, albuterol (salbutamol in Europe) or terbutaline. The beta 2 selectivity of fenoterol at normal oral and inhaled doses is the same as for albuterol and terbutaline. Its pharmacodynamic effects are similar to those of other selective beta 2-adrenoceptor agonists. |
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| DC34301 | SAFit2 | SAFit2 is a selective inhibitor of the ?FK506-binding protein 51 (FKBP51). |
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| DC34303 | NAV26 Featured | NAV 26 (compound 26) is a selective voltage-gated sodium channel Nav1.7 blocker with an IC50 of 0.37 μM. NAV 26 can be used for pain research. |
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| DC34304 | Indatraline HCl | Indatraline HCl is a potent inhibitor of dopamine, norepinephrine and serotonin uptake. |
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| DC34305 | KT185 | KT185 is the first orally-active ABHD6-selective inhibitor. It displays excellent selectivity against other brain and liver serine hydrolases in vivo. |
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| DC34306 | TC-E 5002 | TC-E 5002 is a selective histone demethylase KDM2/7 subfamily inhibitor. |
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| DC34307 | SR-3576 | SR-3576 is a potent JNK3 inhibitor that is highly selective over p38. |
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| DC34308 | MS438 | MS438 is a potent agonist of the TSH receptor (TSHR). |
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| DC34309 | CJB-090 2HCl | CJB-090 2HCl is a dopamine D3 receptor partial agonist. |
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| DC34310 | Methiothepin Maleate | Methiothepin Maleate is an inhibitor of HCV infection and cell-to-cell transmission that acts by targeting the HCV E2 glycoprotein. |
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