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| Catalog | name | Description | price |
|---|---|---|---|
| R-R-4227 | A71623 CAS No.130408-77-4 | A71623/CAS No.130408-77-4, a CCK-4-based peptide, is a potent and highly selective CCK-A full agonist. The IC50s for A-71623 are 3.7 nM in guinea pig pancreas (CCK-A) and 4500 nM in cerebral cortex (CCK-B) in radioligand binding assays, respectively. | price> |
| R-C-2528 | Losartan potassium CAS:124750-99-8 | Losartan potassium(DuP-753 potassium)is an angiotensin II receptor type 1 (AT1)antagonist,competing with the binding of angiotensin II to AT1 with an IC50 of 20nM. | price> |
| R-R-4228 | Lorglumide sodium salt CAS No.1021868-76-7 | Lorglumide sodium salt (CR-1409 sodium salt)/CAS No.1021868-76-7 is a potent cholecystokinin (CCK) receptor antagonist. | price> |
| R-C-2529 | Apalutamide (ARN-509) CAS:956104-40-8 | Apalutamide(ARN-509 and JNJ-56021927)is an androgen receptor antagonist with potential antineoplastic activity.ARN-509 binds to AR in target tissues thereby preventing androgen-induced receptor activation and facilitating the formation of inactive complexes that cannot be translocated to the nucleus.This prevents binding to and transcription of AR-responsive genes.This ultimately inhibits the expression of genes that regulate prostate cancer cell proliferation and may lead to an inhibition of cell growth in AR-expressing tumor cells. | price> |
| R-R-4229 | Lintitript CAS No.136381-85-6 | Lintitript (SR 27897)/CAS No.136381-85-6 is a highly potent, selective, orally active, competitive and non-peptide cholecystokinin (CCK1) receptor antagonist with an EC50 of 6 nM and a Ki of 0.2 nM. Lintitript displays > 33-fold selectivity more selective for CCK1 than CCK2 receptors (EC50 value of 200 nM). Lintitript increases plasma concentration of leptin and food intake as well as plasma concentration of insulin. | price> |
| R-C-2530 | Exemestane (FCE 24304) CAS:107868-30-4 | Exemestane is a synthetic androgen analogue.Exemestane binds irreversibly to and inhibits the enzyme aromatase,thereby blocking the conversion of cholesterol to pregnenolone and the peripheral aromatization of androgenic precursors into estrogens. | price> |
| R-R-4230 | Dexloxiglumide CAS No.119817-90-2 | Dexloxiglumide/CAS No.119817-90-2 is a selective cholecystokinin type A (CCKA) receptor antagonist. Dexloxiglumide, the active enantiomer of Loxiglumide, inhibits smooth muscle cell contractions induced by cholecystokinin-octapeptide (CCK-8). | price> |
| R-C-2531 | Fluticasone propionate CAS:80474-14-2 | Fluticasone propionate,a potent topical anti-inflammatory corticosteroid,is a selective glucocorticoid receptor agonist,with an absolute affinity(KD)of 0.5 nM.Fluticasone propionate shows little or no activity at other steroid receptors.Anti-viral activity. | price> |
| R-R-4231 | CCK-B Receptor Antagonist 2 CAS No.155412-88-7 | CCK-B Receptor Antagonist 2/CAS No.155412-88-7, compound 15b, is a potent and orally active Gastrin/CCK-B antagonist with an IC50 value of 0.43 nM. CCK-B Receptor Antagonist 2 also inhibits gastrin/CCK-A activity with an IC50 of 1.82 μM. | price> |
| R-C-2532 | APD668 CAS:832714-46-2 | APD668 is a potent,selective and orally active agonist of G-protein coupled receptor GPR119,with EC50s of 2.7nM and 33nM for hGPR119 and rGPR119, respectively.APD668 shows no significant inhibition of any of the five major CYP isoforms with the exception of CYP2C9(Ki=0.1μM).APD668 can be used for the research of steatohepatitis and diabetes. | price> |
| R-R-4232 | L-365260 hemihydrate | L-365260 hemihydrate is an orally active and selective antagonist of non-peptide gastrin and brain cholecystokinin receptor (CCK-B), with Kis of 1.9 nM and 2.0 nM, respectively. L-365260 hemihydrate interacts in a stereoselective and competitive manner with guinea pig stomach gastrin and brain CCK receptors. | price> |
| R-C-2533 | Canagliflozin (JNJ 28431754) CAS:842133-18-0 | Canagliflozin(JNJ 28431754)is a selective SGLT2 inhibitor with IC50s of 2nM, 3.7nM,and 4.4nM for mSGLT2,rSGLT2,and hSGLT2 in CHOK cells,respectively. | price> |
| R-R-4233 | (Rac)-Sograzepide CAS No.168161-71-5 | (Rac)-Sograzepide/CAS No.168161-71-5 is an antagonist of cholecystokinin B (CCK-B) receptor, and has the potential of reducing the secretion of gastric acid. | price> |
| R-C-2534 | AMG073 CAS:226256-56-0 | Cinacalcet(AMG073,Sensipar,Cin)is an orally active,allosteric agonist of receptors for calcium(CaR)that increases the sensitivity of the CaR to Ca. | price> |
| R-R-4234 | CCK antagonist 1 CAS No.742116-45-6 | CCK antagonist 1 (compound 3d)/CAS No.742116-45-6 is a CCK antagonist with IC50s of 1.1 μM and 4 μM for CCK1 and CCK2, respectively. CCK antagonist 1 can be used for research of cancer and mental disease. | price> |
| R-C-2535 | Ambrisentan(BSF208075,LU208075) CAS No. 177036-94-1 | Ambrisentan(LU-208075,BSF-208075)is a highly selective antagonist of the endothelin-1 type A receptor,used in the treatment of pulmonary arterial hypertension(PAH). | price> |
| R-R-4235 | AMG 487 CAS No.473719-41-4 | AMG 487/CAS No.473719-41-4 is an orally active and selective antagonist of CXC chemokine receptor 3 (CXCR3) which inhibits the binding of CXCL10 and CXCL11 to CXCR3 with IC50s of 8.0 and 8.2 nM, respectively. | price> |
| R-C-2536 | Canagliflozin hemihydrate CAS:928672-86-0 | Canagliflozin hemihydrate(JNJ28431754 hemihydrate) is a selective SGLT2 inhibitor with IC50s of 2nM,3.7nM,and 4.4nM for mSGLT2, rSGLT2,and hSGLT2 in CHOK cells,respectively. | price> |
| R-R-4236 | Reparixin CAS No.266359-83-5 | Reparixin/CAS No.266359-83-5 is a non-competitive allosteric inhibitor of the chemokine receptors CXCR1 and CXCR2 activation with IC50s of 1 and 100 nM, respectively. | price> |
| R-C-2537 | Ipragliflozin (ASP1941) CAS:761423-87-4 | Ipragliflozin(ASP1941)is an orally active and selective SGLT2 inhibitor with IC50s of 7.38 and 1876nM,6.73 and 1166nM,5.64 and 1380nM for human SGLT2 and SGLT1,rat SGLT2 and SGLT1,mouse SGLT2 and SGLT1,respectively.Antidiabetic agent. | price> |

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