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Filtered Search Results
Aobchem N-methyl-5-(p-tolyl)thiazol-2-amine | 97% | CAS 1600075-40-8 | C11H12N2S | 250mg
N-methyl-5-(p-tolyl)thiazol-2-amine | 97% | CAS 1600075-40-8 | C11H12N2S | 250mg
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Aobchem N-methyl-5-(p-tolyl)thiazol-2-amine | 97% | CAS 1600075-40-8 | C11H12N2S | 1g
N-methyl-5-(p-tolyl)thiazol-2-amine | 97% | CAS 1600075-40-8 | C11H12N2S | 1g
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Chemscene CHEMSCENE
5000576502 ETHYL 2-P-TOLYL ACETATE 5G
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Medchemexpress LLC N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride | 4272-74-6 | 99.0% | 369.31 | 25 MG
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N-alpha-Tosyl-L-lysine chloromethyl ketone (TLCK) is a trypsin-like protease inhibitor that sensitizes HeLa cells to Fas-mediated cell death. It also exhibits an inhibitory effect on IFN-γ activities. This product is for research use only.
- Trypsin-like protease inhibitor
- Sensitizes HeLa cells to Fas-mediated cell death
- Exhibits an inhibitory effect on IFN-γ activities
- Soluble in H2O and DMSO at concentrations ≥ 100 mg/mL (270.78 mM)
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Medchemexpress LLC Pyridine, 4-[4-(4-fluorophenyl)-2-[4-(methylsulfonyl)phenyl]-1H-imidazol-5-yl]- | 152121-46-5 | 98.4% | 393.43 | 10 MM/1 ML
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SB 203580 sulfone is an analog of p38 MAP kinase inhibitor SB 203580. It inhibits IL-1 production (IC50 of 0.2 μM in monocytes), binds competitively with CSAID binding proteins (CSBP), inhibits stress response signaling with an IC50 of 0.03 μΜ, and inhibits 5-LO with an IC50 value of 24 μM. This compound can be used in the research of inflammatory diseases.
- Analog of p38 MAP kinase inhibitor.
- Inhibits IL-1 production (IC50 of 0.2 μM in monocytes).
- Binds competitively with CSAID binding proteins (CSBP).
- Inhibits stress response signaling (IC50 of 0.03 μΜ).
- Inhibits 5-LO (IC50 of 24 μM).
- Suitable for research of inflammatory diseases.
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eMolecules 36635-61-7 | p-Toluenesulfonylmethyl isocyanide | Chem-Impex | MFCD00000005 | 195.240 | C9H9NO2S | 99.000 | Cc1ccc(cc1)S(=O)(=O)C[N+]#[C-] | 100g | 603112008
p-Toluenesulfonylmethyl isocyanide | Chem-Impex | 36635-61-7 | MFCD00000005 | 195.240 | C9H9NO2S | 99.000 | Cc1ccc(cc1)S(=O)(=O)C[N+]#[C-] | 100g | 603112008
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Aobchem 2 4-Difluoro-1-(1-(p-tolyl)ethyl)benzene | ≥95% | CAS 2484888-98-2 | C15H14F2 | 250mg
2 4-Difluoro-1-(1-(p-tolyl)ethyl)benzene | ≥95% | CAS 2484888-98-2 | C15H14F2 | 250mg
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Aobchem 1-Methoxy-4-(1-(p-tolyl)ethyl)benzene | ≥97% | CAS 196489-67-5 | C16H18O | 1g
1-Methoxy-4-(1-(p-tolyl)ethyl)benzene | ≥97% | CAS 196489-67-5 | C16H18O | 1g
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Aobchem Ethyl 2 2-difluoro-2-(p-tolyl)acetate | ≥97% | CAS 131323-06-3 | C11H12F2O2 | 1g
Ethyl 2 2-difluoro-2-(p-tolyl)acetate | ≥97% | CAS 131323-06-3 | C11H12F2O2 | 1g
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Aobchem 1-Methoxy-4-(1-(p-tolyl)ethyl)benzene | ≥97% | CAS 196489-67-5 | C16H18O | 250mg
1-Methoxy-4-(1-(p-tolyl)ethyl)benzene | ≥97% | CAS 196489-67-5 | C16H18O | 250mg
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TARGETMOL CHEMICALS INC Lansoprazole sulfone 5MG
Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Lansoprazole sulfone is a metabolite of the gastric pump inhibitor Lansoprazole. Purity 100%
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Medchemexpress LLC Lansoprazole sulfone | 131926-99-3 | 99.5% | 385.36 | 5 MG
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Lansoprazole sulfone is an orally active and selective inhibitor of H+, K+-ATPase. It can significantly stimulate gastric acid secretion by inhibiting H+, K+-ATPase. This compound has potential applications in duodenal ulcer, gastric ulcer, gastroesophageal reflux disease, and Zolinger Ellison disease.
- Orally active
- Selective inhibitor of H+, K+-ATPase
- Significantly stimulates gastric acid secretion by inhibiting H+, K+-ATPase
- Potential applications in duodenal ulcer, gastric ulcer, gastroesophageal reflux disease, and Zolinger Ellison disease
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Medchemexpress LLC 2-[[4-(3-methoxypropoxy)-3-methyl-2-pyridinyl]methylsulfonyl]-1H-benzimidazole | 117976-47-3 | MFCD08063743 | 1g
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Rabeprazole sulfone is a metabolite of the proton pump inhibitor Rabeprazole and is an impurity reference for Rabeprazole[1]
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Medchemexpress LLC Lansoprazole sulfone | 131926-99-3 | 99.5% | 385.36 | 100 MG
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Lansoprazole sulfone (AG-1813) is an orally active and selective inhibitor of H+, K+-ATPase. It significantly stimulates gastric acid secretion by inhibiting H+, K+-ATPase. It has potential applications in duodenal ulcer, gastric ulcer, gastroesophageal reflux disease, and Zollinger-Ellison disease. It is for research use only and not sold to patients.
- Orally active and selective inhibitor of H+, K+-ATPase.
- Significantly stimulates gastric acid secretion by inhibiting H+, K+-ATPase.
- Potential applications in duodenal ulcer, gastric ulcer, gastroesophageal reflux disease, and Zollinger-Ellison disease.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC N-Boc-O-tosyl hydroxylamine | 105838-14-0 | MFCD22201097 | 287.33 | 5 G
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N-Boc-O-tosyl hydroxylamine is a safe and efficient nitrogen source for N-amination of aryl and alkyl amines. It promotes electrophilic N-amination of aryl amines and alkyl amines to generate β-Boc-protected aryl hydrazines and alkyl hydrazines.
- Safe and efficient nitrogen source
- Promotes electrophilic N-amination of aryl amines
- Promotes electrophilic N-amination of alkyl amines
- Generates β-Boc-protected aryl hydrazines
- Generates β-Boc-protected alkyl hydrazines
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