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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000377808 RAVOXERTINIB HYDROCH 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000377574 SAG-524 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000377485 SSRNA41 SODIUM 1MG
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eMolecules 128-08-5 | N-Bromosuccinimide (< 0.1% wt chlorine content) | Oakwood Chemical | MFCD00005510 | 177.985 | C4H4BrNO2 | 99.000 | BrN1C(=O)CCC1=O | 25g | 705862206
N-Bromosuccinimide (< 0.1% wt chlorine content) | Oakwood Chemical | 128-08-5 | MFCD00005510 | 177.985 | C4H4BrNO2 | 99.000 | BrN1C(=O)CCC1=O | 25g | 705862206
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Medchemexpress LLC 1,4,7,10-Tetraazacyclododecane | 294-90-6 | 172.28 | 25 G
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1,4,7,10-Tetraazacyclododecane | 294-90-6 | 172.28 | 25 G
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Medchemexpress LLC 2,4,6-Trihydroxybenzaldehyde | 487-70-7 | 154.12 | 25 G
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2,4,6-Trihydroxybenzaldehyde is an orally active NF-κB inhibitor that demonstrates anti-tumor, anti-cancer cell proliferative, and anti-obesity activities. It inhibits adipocyte differentiation and lipid accumulation in 3T3-L1 cells and down-regulates PPARγ, C/EBPα, SREBP-1c, and FAS protein expression levels. In vivo, oral administration reduces high-fat diet-induced weight gain and lowers serum levels of glucose, triglycerides, and total cholesterol.
- Inhibits adipocyte differentiation
- Reduces lipid accumulation
- Down-regulates PPARγ, C/EBPα, SREBP-1c, and FAS protein expression
- Reduces high-fat diet-induced weight gain
- Lowers serum levels of glucose, triglycerides, and total cholesterol
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383268 LEVOMEDETOMIDINE HY 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000381579 DISUFENTON SODIUM 10MM 1ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383135 NECROSTATIN-34 10MM 1ML
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eMolecules 128-08-5 | N-Bromosuccinimide | AA Blocks LLC | MFCD00005510 | 177.985 | C4H4BrNO2 | 0.000 | BrN1C(=O)CCC1=O | 100g | 410148706
N-Bromosuccinimide | AA Blocks LLC | 128-08-5 | MFCD00005510 | 177.985 | C4H4BrNO2 | 0.000 | BrN1C(=O)CCC1=O | 100g | 410148706
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eMolecules 551-93-9 | 2'-Aminoacetophenone | Apollo Scientific US - Building Blocks | MFCD00007717 | 135.166 | C8H9NO | 95.000 | CC(=O)c1ccccc1N | 100g | 398006245
2'-Aminoacetophenone | Apollo Scientific US - Building Blocks | 551-93-9 | MFCD00007717 | 135.166 | C8H9NO | 95.000 | CC(=O)c1ccccc1N | 100g | 398006245
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Alkali Scientific Magenta Gal [5 Bromo 6 chloro 3 indolyl β D galactopyranoside], 100 Mg
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Magenta Gal (5 Bromo 6 chloro 3 indolyl β D galactopyranoside) is a chromogenic substrate designed for laboratory use in the detection of galactosidase activity. This 100 mg reagent is widely used in biochemical assays where the presence of β-galactosidase is of interest. The compound reacts with the enzyme to produce a colorimetric change, allowing for the identification and quantification of enzyme activity. It is commonly used in microbiological assays, gene expression studies, and diagnostic tests where the detection of β-galactosidase is required for understanding enzyme function and metabolic processes in cells and organisms.
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eMolecules 202865-59-6 | 2-Bromo-4,6-difluoroanisole | Ambeed | MFCD00070754 | 223.017 | C7H5BrF2O | 98.000 | COc1c(F)cc(F)cc1Br | 5g | 552552809
2-Bromo-4,6-difluoroanisole | Ambeed | 202865-59-6 | MFCD00070754 | 223.017 | C7H5BrF2O | 98.000 | COc1c(F)cc(F)cc1Br | 5g | 552552809
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eMolecules 516-12-1 | N-Iodosuccinimide | AA Blocks LLC | MFCD00005512 | 224.985 | C4H4INO2 | 0.000 | IN1C(=O)CCC1=O | 25g | 410168214
N-Iodosuccinimide | AA Blocks LLC | 516-12-1 | MFCD00005512 | 224.985 | C4H4INO2 | 0.000 | IN1C(=O)CCC1=O | 25g | 410168214
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Medchemexpress LLC Diphenylmethanimine | 1013-88-3 | 181.23 | 500 G
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Diphenylmethanimine is a biochemical reagent useful in life science related research. It serves as a biological material or organic compound, applicable in the preparation of nitrogen ylide dimers, and as an ammonia surrogate, also functioning as an intermediate for organic chemical synthesis.
- Useful in the preparation of nitrogen ylide dimers.
- Functions as a benzophenone imine as ammonia surrogate.
- An intermediate material for the synthesis of organic chemicals.
- Catalytic enantioselective alkylation of the benzophenone imine of glycine t-butyl ester using phosphazene (Schwesinger) bases and chiral quaternary ammonium salts yields either enantiomer of amino acid derivatives in excellent yield.
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