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| Catalog | name | Description | price |
|---|---|---|---|
| R-R-3778 | Bevantolol hydrochloride CAS No.42864-78-8 | Bevantolol hydrochloride/CAS No.42864-78-8 is a selective β1 and α1-adrenergic receptor antagonist with pKi values of 7.83, 6.9 in rat cerebral cortex, respectively. Bevantolol hydrochloride is a potent Ca2+ antagonist. | price> |
| R-C-2079 | E-7046 CAS:1369489-71-3 | E7046 is an orally bioavailable and specific EP4 antagonist,with IC50 of 13.5nM and Ki of 23.14nM,exhibiting anti-tumor activities. | price> |
| R-R-3779 | Bambuterol hydrochloride CAS No.81732-46-9 | Bambuterol hydrochloride/CAS No.81732-46-9 ((±)-Bambuterol hydrochloride; KWD-2183 hydrochloride) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a proagent of terbutaline. | price> |
| R-C-2080 | Bemcentinib (R428) CAS:1037624-75-1 | Bemcentinib(R428,BGB324)is an inhibitor of Axl with IC50 of 14 nM,>100-fold selective for Axl versus Abl.Selectivty for Axl is also greater than Mer and Tyro3(50-to-100- fold more selective)and InsR,EGFR,HER2,and PDGFRβ(100- fold more selective). | price> |
| R-R-3780 | Dabuzalgron CAS No.219311-44-1 | Dabuzalgron (Ro 115-1240)/CAS No.219311-44-1 is an orally active and selective α-1A adrenergic receptor agonist for the treatment of urinary incontinence. Dabuzalgron protects against Doxorubicin-induced cardiotoxicity by preserving mitochondrial function. | price> |
| R-C-2081 | CPI-444 CAS:1202402-40-1 | Ciforadenant(CPI-444,V81444)is a potent and selective Adenosine A2A receptor antagonist.It binds to A2A receptors with a Ki of 3.54 nmol/L and demonstrates a greater than 50-fold selectivity for the A2A receptor over other adenosine receptor subtypes. | price> |
| R-R-3781 | Esmolol hydrochloride CAS No.81161-17-3 | Esmolol hydrochloride/CAS No.81161-17-3 is a beta adrenergic receptor blocker. | price> |
| R-C-2082 | ars-1620 CAS:1698055-85-4 | ARS-1620 is a potent,orally bioavailable covalent inhibitor of KRAS-G12C and could achieve rapid and sustained in vivo target occupancy to induce tumor regression. | price> |
| R-R-3782 | Glaucine CAS No.475-81-0 | Glaucine (O,O-Dimethylisoboldine)/CAS No.475-81-0 is an alkaloid isolated from Glaucium flavum with antitussive, bronchodilation and anti-inflammatory properties. Glaucine is a selective and orally active phosphodiesterase 4 (PDE4) inhibitor with Kis of 3.4 µM in human bronchus and polymorphonuclear leukocytes. Glaucine is also a non-selective α-adrenoceptor antagonist, a Ca2+ entry blocker, and a weak dopamine D1 and D2 receptor antagonist. Glaucine has antioxidative and antiviral activities. | price> |
| R-C-2083 | USP25 and 28 inhibitor AZ-1 CAS:2165322-94-9 | USP25/28 inhibitor AZ1(AZ1)is an orally active,selective,noncompetitive, dual ubiquitin specific protease(USP)25/28 inhibitor with IC50s of 0.7μM and 0.6 μM,respectively.USP25/28 inhibitor AZ1 attenuates colitis and tumorigenesis in the mice model. | price> |
| R-R-3783 | Detomidine hydrochloride CAS No.90038-01-0 | Detomidine hydrochloride/CAS No.90038-01-0, an imidazole derivative, is a potent α2-adrenergic agonist. Detomidine hydrochloride produces dose-dependent analgesic effects. | price> |
| R-C-2084 | Belvarafenib (HM95573) CAS:1446113-23-0 | Belvarafenib(GDC5573,HM95573,RG6185)is a selective and orally bioavailable pan-RAF kinase inhibitor with IC50 values of 41 nM,7nM and 2nM for BRAF WT, BRAF(V600E)and CRAF kinases,respectively. | price> |
| R-R-3784 | Hydrocortisone 17-butyrate CAS No.13609-67-1 | Hydrocortisone 17-butyrate/CAS No.13609-67-1 is an adrenocortical hormone active molecule. | price> |
| R-C-2085 | Q-VD-OPh hydrate CAS:1135695-98-5 | Q-VD-OPh is an irreversible pan-caspase inhibitor with potent antiapoptotic properties,inhibits caspase 7 with an IC50 of 48nM and 25-400nM for other caspases including caspase 1,3,8,9,10,and 12.Q-VD-OPh can inhibits HIV infection.Q-VD-OPh is able to cross the blood-brain barrier. | price> |
| R-R-3785 | Ro 363 hydrochloride CAS No.250580-70-2 | Ro 363 hydrochloride/CAS No.250580-70-2, an effective inotropic stimulant, is a potent and highly selective β1-adrenoceptor agonist. Ro 363 hydrochloride is a cardiovascular modulator that reduces diastolic blood pressure and pronounces increases in myocardial contractility. | price> |
| R-C-2086 | GSK2983559 FREE ACID CAS:1579965-12-0 | GSK2983559 free acid(compound 3)is a potent,specific and oral active receptor interacting protein 2(RIP2)kinase inhibitor.GSK2983559 free acid has excellent activity in blocking many proinflammatory cytokine responses in vivo and in human inflammatory bowel disease explant samples. | price> |
| R-R-3786 | Lofexidine CAS No.31036-80-3 | Lofexidine/CAS No.31036-80-3 is a selective α2-receptor agonist, commonly used to alleviate the physical symptoms of heroin and other types of opioid withdrawal. | price> |
| R-C-2087 | Elexacaftor (VX-445) CAS:2216712-66-0 | Elexacaftor(VX-445,Compound 1)is a modulator of cystic fibrosis transmembrane conductance regulator(CFTR).Elexacaftor(VX-445,Compound 1)facilitates the processing and trafficking of CFTR to increase the amount of CFTR at the cell surface. | price> |
| R-R-3787 | Tulobuterol CAS No.41570-61-0 | Tulobuterol (C-78 free base)/CAS No.41570-61-0 is a long-acting β2-adrenoceptor agonist, which reduces the frequency of exacerbations of chronic obstructive pulmonary disease and bronchial asthma. Tulobuterol is also a sympathomimetic agent used as a transdermal patch, and increases normal diaphragm muscle strength. | price> |
| R-C-2088 | azd4635 CAS:1321514-06-0 | AZD4635(HTL1071)is a potent,selective and orally active adenosine A2A receptor(A2AR)antagonist.AZD4635 binds to human A2AR with a Ki of 1.7nM and shows>30-fold selectivity over other adenosine receptors. | price> |

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