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R-C-2205 SU5214 CAS: 186611-04-1 SU5214 is a potent VEGFR2 inhibitor extracted from patent US5834504A,SU5214, has IC50s of 14.8µM(FLK-1)and 36.7µM(EGFR),respectively. price>
R-R-3905 Efaroxan hydrochloride CAS No.89197-00-2 Efaroxan hydrochloride/CAS No.89197-00-2 is a potent, selective and orally active α2-adrenoceptor antagonist, with antidiabetic activity. Efaroxan hydrochloride is a selective I1-Imidazoline receptor antagonist. Efaroxan hydrochloride can be used for the research of cardiovascular disease. price>
R-C-2206 SU5408 CAS:15966-93-5 SU5408(VEGFR2 Kinase Inhibitor I)is a potent and cell-permeable inhibitor of VEGFR2 kinase with an IC50 of 70nM. price>
R-R-3906 NP10679 NP10679 is a selective, pH dependent GluN2B subunit-specific N-methyl-D-aspartate (NMDA) receptor inhibitor with high oral bioavailability and good brain penetration. NP10679 inhibits GluN2B with IC50s of 23 and 142 nM at pH 6.9 and 7.6, respectively. NP10679 is a histamine H1 antagonist and a hERG channel inhibitor with IC50s of 73 and 620 nM, respectively. NP10679 is a reversible inhibitor of human liver CYP enzymes. price>
R-C-2207 SU5205 CAS:3476-86-6 SU5205 is an inhibitor of VEGFR2 (FLK-1),with an IC50 of 9.6μM. price>
R-R-3907 Scopine hydrochloride CAS No.85700-55-6 Scopine hydrochloride (6,7-Epoxytropine hydrochloride)/CAS No.85700-55-6 is the metabolite of anisodine, which is a α1-adrenergic receptor agonist and used in the treatment of acute circulatory shock. price>
R-C-2208 2-D08 CAS:144707-18-6 2-D08 is a cell permeable,mechanistically unique inhibitor of protein sumoylation.It is also inhibits Axl,IRAK4,ROS1,MLK4,GSK3β,RET,KDR and PI3Kα with IC50 values of 0.49,3.9,5.3,9.8,11,11,17 and 35nM respectively in biochemical assays. price>
R-R-3908 Bunazosin CAS No.80755-51-7 Bunazosin/CAS No.80755-51-7 is a potent and selective α1-adrenoceptor antagonist. Bunazosin can be used for antihypertensive and ocular hypotensive research. price>
R-C-2209 CS-2660 (JNJ-38158471) CAS:951151-97-6 CS-2660(JNJ-38158471)is a well tolerated,orally available,highly selective VEGFR-2 inhibitor with IC50 of 40 nM.CS-2660(JNJ-38158471)also inhibits closely related tyrosine kinases such as RET(c-RET)and Kit(c-Kit)with IC50 of 180nM and 500nMwhile it has no significant activity(>1 microM) against VEGFR-1 and VEGFR-3. price>
R-R-3909 Salbutamol-d3 CAS No.1219798-60-3 Salbutamol-d3/CAS No.1219798-60-3 is the deuterium labeled Salbutamol. Salbutamol is a short-acting β2-adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and chronic obstructive pulmonary disease (COPD). price>
R-C-2210 Ningetinib CAS:1394820-69-9 Ningetinib is a potent,orally bioavailable small molecule tyrosine kinase inhibitor(TKI)with IC50s of 6.7,1.9 and<1.0nM for c-Met,VEGFR2 and Axl,respectively. price>
R-R-3910 Midaglizole CAS No.66529-17-7 Midaglizole ((±)-DG5128 free base, DG5128 free base)/CAS No.66529-17-7 is a potent α2-adrenoceptor antagonist. Midaglizole is a hypoglycemic agent. Midaglizole increases blood pressure and reduces blood glucose levels in vivo. price>
R-C-2211 CZC-8004 CAS:916603-07-1 CZC-8004 is a pan-kinase inhibitor and binds a range of tyrosine kinases, including ABL kinase. price>
R-R-3911 ICI 89406 CAS No.53671-71-9 ICI 89406/CAS No.53671-71-9 is a selective β1 adrenergic receptor antagonist amenable to labelling with positron emitters, for PET. price>
R-C-2212 AG-13958 CAS:319460-94-1 AG-13958(AG-013958),a potent VEGFR tyrosine kinase inhibitor,is used for treatment of choroidal neovascularization associated with age-related macular degeneration(AMD). price>
R-R-3912 Phenylephrine-2,4,6-d3 hydrochloride CAS No.1276197-50-2 Phenylephrine-2,4,6-d3 (hydrochloride)/CAS No.1276197-50-2 is the deuterium labeled Phenylephrine hydrochloride. (R)-(-)-Phenylephrine hydrochloride is a selective α1-adrenoceptor agonist with pKis of 5.86, 4.87 and 4.70 for α1D, α1B and α1A receptors respectively. price>
R-C-2213 Donafenib (Sorafenib D3) CAS:1130115-44-4 Sorafenib(D3)(Bay 43-9006 (D3))is the deuterium labeled Sorafenib.Sorafenib is a multikinase inhibitor IC50s of 6nM,20nM,and 22nM for Raf-1, B-Raf,and VEGFR-3, respectively. price>
R-R-3913 Amosulalol CAS No.85320-68-9 Amosulalol (YM 09538)/CAS No.85320-68-9 is an orally active and dual inhibitor of α1/β1-Adrenergic Receptor. Amosulalol exhibits antihypertensive activity via α1-Adrenergic Receptor inhibition. Amosulalol decreases reflexogenic increases in heart rate and plasma renin activity (PRA) via β1-Adrenergic Receptor inhibition in spontaneously hypertensive rats (SHR). price>
R-C-2214 SKLB 610 CAS:1125780-41-7 SKLB610 is a VEGFR inhibitor that potently suppresses human tumor angiogenesis. SKLB610 inhibited angiogenesis-related tyrosine kinase VEGFR2,fibroblast growth factor receptor 2(FGFR2)and platelet-derived growth factor receptor(PDGFR)at rate of 97%,65% and 55%,respectively,at concentration of 10μM in biochemical kinase assays.SKLB610 exhibited its antitumor activity as a multi-targeted inhibitor with more potent inhibition of VEGFR2 activity. price>
R-R-3914 Yohimbine-13C,d3 CAS No.1261254-59-4 Yohimbine-13C,d3/CAS No.1261254-59-4 is the 13C- and deuterium labeled Yohimbine. Yohimbine is a potent and relatively nonselective alpha 2-adrenergic receptor (AR) antagonist, with IC50 of 0.6 μM. price>