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| Catalog | name | Description | price |
|---|---|---|---|
| R-R-3799 | Guanadrel CAS No.40580-59-4 | Guanadrel/CAS No.40580-59-4 is an orally active postganglionic adrenergic inhibitor of spiroketal. Guanadre can be used in anti-hypertensive studies. | price> |
| R-C-2100 | CT-1812 CAS:1802632-22-9 | CT-1812 is a first-in-class,orally available sigma-2/PGRMC1 antagonist(alpha beta oligomer receptor antagonist),is being developed by Cognition.sCT-1812 is a novel therapeutic candidate for Alzheimer is disease. | price> |
| R-R-3800 | LY377604 CAS No.204592-94-9 | LY377604/CAS No.204592-94-9 is a human β3-adrenergic receptor agonist with an EC50 of 2.4 nM and also a β1- and β2-adrenergic receptor antagonist. | price> |
| R-C-2101 | BAY-545 CAS:1699717-32-2 | BAY-545 is a potent and selective A2B adenosine receptor antagonist, with an IC50 of 59 nM. BAY-545 also exhibits IC50s of 66,400,280 nM for human, mouse,rat A2B adenosine receptor in cells,respectively,and a Ki of 97nM for human A2B adenosine receptor,with more selectivity over A1,A2A,and A3 adenosine receptor. | price> |
| R-R-3801 | Apraclonidine hydrochloride CAS No.73218-79-8 | Apraclonidine hydrochloride (ALO 2145)/CAS No.73218-79-8, a selective α2 and weak α1 receptor agonist activity, effectively lowers intraocular pressure (IOP) in human eyes. Apraclonidine hydrochloride is a topical ophthalmic solution and has the ability to elevate the eye lid. | price> |
| R-C-2102 | Ingliforib CAS:186392-65-4 | Ingliforib is a glycogen phosphorylase inhibitor,with IC50s of 52,352 and 150nM for liver,muscle and brain glycogen phosphorylase,and has cardioprotective activity. | price> |
| R-R-3802 | Tizanidine hydrochloride CAS No.64461-82-1 | Tizanidine hydrochloride/CAS No.64461-82-1 is an α2-adrenergic receptor agonist and inhibits neurotransmitter release from CNS noradrenergic neurons. | price> |
| R-C-2103 | Batefenterol CAS:743461-65-6 | Batefenterol(GSK961081;TD-5959)is a novel muscarinic receptor antagonist and β2-adrenoceptor agonist;displays high affinity for hM2,hM3 muscarinic and hβ2-adrenoceptor with Ki values of 1.4,1.3 and 3.7nM,respectively. | price> |
| R-R-3803 | Lofexidine hydrochloride CAS No.21498-08-8 | Lofexidine (hydrochloride)/CAS No.21498-08-8 is a selective α2-receptor agonist, commonly used to alleviate the physical symptoms of heroin and other types of opioid withdrawal. | price> |
| R-C-2104 | BAR 502 CAS:1612191-86-2 | BAR502 is a dual FXR and GPBAR1 agonist.BAR-502 promotes browning of white adipose tissue and reverses liver steatosis and fibrosis.BAR502 protects against liver damage caused by HFD by promoting the browning of adipose tissue. | price> |
| R-R-3804 | Ritodrine hydrochloride CAS No.23239-51-2 | Ritodrine (DU21220) hydrochloride/CAS No.23239-51-2 is a β-adrenergic agonist, also an effective smooth muscle and uterine relaxant. Ritodrine hydrochloride prolongs contraction interval, can be used for researching arrest premature labor. | price> |
| R-C-2105 | BAR 501 CAS: 1632118-69-4 | BAR501 is a potent and selective G protein-coupled bile acid receptor 1(GPBAR1, GPCR19,TGR5)agonist that effectively transactivates GPBAR1 in HEK293 cells overexpressing a CRE along with GPBAR1 with EC50 of 1μM. | price> |
| R-R-3805 | Indoramin CAS No.26844-12-2 | Indoramin/CAS No.26844-12-2 is an orally active antihypertensive agent. Indoramin is also selective for the α1A-adrenoceptor. | price> |
| R-C-2106 | GSK3117391 CAS:1018673-42-1 | GSK3117391(GSK3117391A)and HDAC-IN-3,is a potent HDAC inhibitor for treating chronic inflammatory disorders. | price> |
| R-R-3806 | Bucindolol CAS No.71119-11-4 | Bucindolol/CAS No.71119-11-4 is a β1-adrenergic receptor blocker, with intrinsic sympathomimetic activity, used in the research of heart failure. | price> |
| R-C-2107 | PZ-2891 CAS:2170608-82-7 | PZ-2891 is an orally bioavailable,brain penetrant pantothenate kinase (PANK)modulator.PZ-2891 act as an orthosteric inhibitor at high concentrations and an allosteric activator at lower sub-saturating concentrations.PZ-2891 inhibits human pantothenate kinases PANK1β,PANK2,and PANK3 with IC50s of 40.2 nM,0.7nM and 1.3nM,respectively. | price> |
| R-R-3807 | (R)-Terazosin CAS No.109351-34-0 | (R)-Terazosin/CAS No.109351-34-0 is an active R-enantiomer of Terazosin. (R)-Terazosin is a potent α1-adrenoceptor antagonist with Ki values of 6.51 nM, 1.01 nM and 1.97 nM for α1a, α1b and α1d-adrenoceptor, respectively. | price> |
| R-C-2108 | LJ570 CAS:2252488-69-8 | LJ570 is the first PPARα/γDual Agonist Able To Bind to Canonical and Alternative Sites of PPARγ and To Inhibit Its Cdk5-Mediated Phosphorylation. LJ570 is a potent partial agonist of both PPARα and γ subtypes.LJ570 inhibited the Cdk5-mediated phosphorylation of PPARγ at serine 273 that is currently considered the mechanism by which some PPARγ partial agonists exert antidiabetic effects similar to thiazolidinediones,without showing their typical side effects.LJ570 may be useful for treatment of dyslipidemic type 2 diabetes. | price> |
| R-R-3808 | Phentolamine CAS No.50-60-2 | Phentolamine/CAS No.50-60-2 is a potent, selective and orally active α1 adrenergic and α2 adrenergic receptor antagonist. Phentolamine can be used for the research of erectile dysfunction. | price> |
| R-C-2109 | AWZ1066S CAS:2239272-16-1 | AWZ1066S is a highly specific anti-Wolbachia drug candidate for a short-course treatment of filariasis,with an EC50 of 2.5nM in cell assay. | price> |

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