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Filtered Search Results
Aobchem 2 3-Dihydro-N-(1-methylethyl)-1 4-benzodioxin-6-sulfonamide | 95% | CAS 333453-79-5 | C11H15NO4S | 500mg
2 3-Dihydro-N-(1-methylethyl)-1 4-benzodioxin-6-sulfonamide | 95% | CAS 333453-79-5 | C11H15NO4S | 500mg
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eMolecules 1965304-73-7 | 2-(2-Pyridyl)-4-(2-hydroxyphenyl)thiazole | Oakwood Chemical | MFCD28166215 | 254.310 | C14H10N2OS | 97.000 | Oc1ccccc1-c1csc(n1)-c1ccccn1 | 5g | 537706222
2-(2-Pyridyl)-4-(2-hydroxyphenyl)thiazole | Oakwood Chemical | 1965304-73-7 | MFCD28166215 | 254.310 | C14H10N2OS | 97.000 | Oc1ccccc1-c1csc(n1)-c1ccccn1 | 5g | 537706222
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Aobchem -Dimethyl-3-(1-methylethyl)benzenemethanol | ≥95% | CAS 14860-89-0 | C12H18O | 250mg
-Dimethyl-3-(1-methylethyl)benzenemethanol | ≥95% | CAS 14860-89-0 | C12H18O | 250mg
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![Aobchem 4-[(1-Methylethyl)thio]benzenemethanol | ≥97% | CAS 152595-89-6 | C10H14OS | 250mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000960321.png-250.jpg)
Aobchem 4-[(1-Methylethyl)thio]benzenemethanol | ≥97% | CAS 152595-89-6 | C10H14OS | 250mg
4-[(1-Methylethyl)thio]benzenemethanol | ≥97% | CAS 152595-89-6 | C10H14OS | 250mg
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Aobchem (2-(Ethoxycarbonyl)-4-fluorophenyl)boronic acid | ≥95% | CAS 1072951-40-6 | C9H10BFO4 | 5g
(2-(Ethoxycarbonyl)-4-fluorophenyl)boronic acid | ≥95% | CAS 1072951-40-6 | C9H10BFO4 | 5g
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![Aobchem 3-[4-(1-Methylethyl)phenyl]-2-propynoic acid | ≥95% | CAS 1181589-49-0 | C12H12O2 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000974111.png-250.jpg)
Aobchem 3-[4-(1-Methylethyl)phenyl]-2-propynoic acid | ≥95% | CAS 1181589-49-0 | C12H12O2 | 1g
3-[4-(1-Methylethyl)phenyl]-2-propynoic acid | ≥95% | CAS 1181589-49-0 | C12H12O2 | 1g
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Aobchem -Methyl- -(1-methylethyl)-3-(methylthio)benzenemethanol | ≥95% | CAS 1379311-12-2 | C12H18OS | 5g
-Methyl- -(1-methylethyl)-3-(methylthio)benzenemethanol | ≥95% | CAS 1379311-12-2 | C12H18OS | 5g
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Aobchem 6-Chloro- -(1-methylethyl)-3-pyridinemethanol | 97% | CAS 1525037-90-4 | C9H12ClNO | 250mg
6-Chloro- -(1-methylethyl)-3-pyridinemethanol | 97% | CAS 1525037-90-4 | C9H12ClNO | 250mg
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Aobchem 4-Ethoxycarbonyl-2-methoxyphenylboronic acid | ≥97% | CAS 603122-86-7 | C10H13BO5 | 10g
4-Ethoxycarbonyl-2-methoxyphenylboronic acid | ≥97% | CAS 603122-86-7 | C10H13BO5 | 10g
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Aobchem 1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 5g
1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 5g
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Aobchem 1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 1g
1-Methylethyl 2-cyano-3-(4-fluorophenyl)-2-propenoate | 95% | CAS 328262-43-7 | C13H12FNO2 | 1g
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Aobchem 2-(1-Methylethyl)-1 1 -biphenyl | 95% | CAS 19486-60-3 | C15H16 | 500mg
2-(1-Methylethyl)-1 1 -biphenyl | 95% | CAS 19486-60-3 | C15H16 | 500mg
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Aobchem 3 4-Dichloro-N-(1-methylethyl)benzenesulfonamide | 95% | CAS 28298-41-1 | C9H11Cl2NO2S | 500mg
3 4-Dichloro-N-(1-methylethyl)benzenesulfonamide | 95% | CAS 28298-41-1 | C9H11Cl2NO2S | 500mg
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Apexbio Technology LLC nor-Binaltorphimine dihydrochloride 113158-34-2 50mg
nor-Binaltorphimine dihydrochloride (CAS 113158-34-2) is a highly selective antagonist of the -opioid receptor By inhibiting -opioid receptor-mediated signaling pathways this compound modulates processes such as nociceptive transmission and regulation of affective states Its selectivity enables precise investigation of -opioid receptor function in experimental models nor-Binaltorphimine dihydrochloride is widely utilized in pain research and neuroscience to elucidate the physiological and behavioral roles of -opioid receptor signaling
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Apexbio Technology LLC IT1t dihydrochloride 1092776-63-0 5mg
IT1t dihydrochloride (CAS 1092776-63-0) is a small-molecule antagonist targeting the chemokine receptor CXCR4 It is designed to inhibit CXCR4-mediated signaling by disrupting interactions with its natural ligand CXCL12 as well as the HIV envelope protein gp120 thereby interfering with cellular chemotaxis and viral entry mechanisms IT1t dihydrochloride exerts its biological activity primarily by antagonizing CXCR4 to inhibit receptor-mediated Ca2 mobilization and virus attachment In in vitro assays IT1t dihydrochloride demonstrates potent inhibition with IC50 values of approximately 8 nM in human CXCR4 receptor binding assays 1 1 nM in Ca2 mobilization assays and 7 nM in HIV attachment assays Based on these pharmacological properties IT1t dihydrochloride holds research potential in CXCR4-related signaling and HIV entry studies
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