Environmental Testing Standards
eMolecules 75418-74-5 | Ambeed | Methyl 3-oxo-3-(pyridin-2-yl)propanoate | 1g | 490513745 | A150317 | MFCD11849520 | 179.175 | C9H9NO3
Ambeed | Methyl 3-oxo-3-(pyridin-2-yl)propanoate | 1g | 490513745 | A150317 | 75418-74-5 | MFCD11849520 | 179.175 | C9H9NO3
Apexbio Technology LLC Mefenamic Acid 61-68-7 10g
Mefenamic acid (CAS 61-68-7) is a non-steroidal anti-inflammatory compound that acts by inhibiting cyclooxygenase (COX) enzymes leading to decreased synthesis of prostaglandins involved in inflammation and pain signaling It is extensively studied for its ability to modulate inflammatory pathways and is commonly utilized as a pharmacological tool in research focused on pain mechanisms inflammatory responses and prostaglandin-mediated processes Mefenamic acid is often employed in in vitro and in vivo models to evaluate the effects of COX inhibition on physiological and pathological conditions
Crescent Chemical Co Inc AGAR AGAR SERVA HIGH GEL
Agar Agar SERVA high gel-strength powder research grade Choice quality for in vitro culture of plants or bacteriology, no turbidity with phosphates. Size - 1KG Storage Conditions - +15 °C TO +30 °C Catalog Number - 11396.03 CAS 9002-18-0
Crescent Chemical Co Inc Ethylenediamine Tetraacetic Acid, 6381-92-6, MFCD00150037, 100g
Molecular Formula C10H14N2O8.2Na.2H2O, Molecular Weight 372.236, Analytical Grade, Storage Conditions: +15 °C TO +30 °C
eMolecules 713-57-5 | ChemScene | 4-(Ethoxycarbonyl)benzoic acid | 250mg | 572281933 | CS-0061577 | MFCD00496597 | 194.186 | C10H10O4
ChemScene | 4-(Ethoxycarbonyl)benzoic acid | 250mg | 572281933 | CS-0061577 | 713-57-5 | MFCD00496597 | 194.186 | C10H10O4
eMolecules AstaTech / 5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER / 1g / 112536086 / E58696 / 97.000 / 72030-87-6 / MFCD02179429 / 262.221 / C12H10N2O5
AstaTech / 5-(4-NITRO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER / 1g / 112536086 / E58696 / 97.000 / 72030-87-6 / MFCD02179429 / 262.221 / C12H10N2O5
Apexbio Technology LLC Naproxen Sodium 26159-34-2 10g
Naproxen sodium (CAS 26159-34-2) is a non-selective cyclooxygenase (COX) inhibitor that suppresses both COX-1 and COX-2 activity In vitro it exhibits IC50 values of 35 48 mol/L for COX-1 and 64 62 mol/L for COX-2 Naproxen sodium influences satellite cell biology by affecting proliferation fusion and differentiation particularly when both COX-1 and COX-2 are inhibited In HCA-7 colon cancer cells naproxen reduces cell viability with an IC50 of 1 45 0 07 M after 48-hour exposure Clinically repeated dosing in volunteers results in substantial inhibition of COX isoforms while research in menstrual migraine models shows significant reductions in headache parameters
eMolecules 517870-18-7 | ChemScene | Methyl 5-(3-nitrophenyl)isoxazole-3-carboxylate | 1g | 632284645 | CS-0150739 | MFCD03778971 | 248.194 | C11H8N2O5
ChemScene | Methyl 5-(3-nitrophenyl)isoxazole-3-carboxylate | 1g | 632284645 | CS-0150739 | 517870-18-7 | MFCD03778971 | 248.194 | C11H8N2O5
Cambridge Isotope Laboratories GLYCAN-GNLACNAC UNLABELED, 500 PMOL
GLYCAN-GNLACNAC UNLABELED, 500 PMOL
Apexbio Technology LLC Trimethoprim 738-70-5 10g
Trimethoprim (CAS 738-70-5) is a small-molecule inhibitor targeting bacterial dihydrofolate reductase (DHFR) It is designed to selectively inhibit DHFR thereby disrupting folate metabolism and nucleic acid synthesis in bacteria Trimethoprim exerts its biological activity primarily through competitive inhibition of bacterial DHFR In experimental studies trimethoprim demonstrates inhibitory activity with IC50 values ranging from approximately 5 to 15 nM against bacterial DHFR enzymes Based on these pharmacological properties trimethoprim holds research potential in studies of microbiology urinary tract infections bacterial metabolism folate biosynthesis antimicrobial resistance and in the pharmacological profiling of antibacterial agents
Apexbio Technology LLC Fuchsine base monohydrochloride 632-99-5 10g
Fuchsine base monohydrochloride (632-99-5) is a synthetic dye belonging to the triphenylmethane family It is designed for staining applications to visualize cellular and tissue components in histological and cytological studies Fuchsine base monohydrochloride exerts its biological activity primarily through binding with negatively charged groups particularly carboxyl-rich sites within cell structures Based on these properties Fuchsine base monohydrochloride holds research potential in biomedical cytological and histological applications for the analysis of tissue morphology cellular anatomy and biological process visualization
eMolecules 126937-43-7 | ChemScene | 1-Benzyl 2-methyl piperazine-12-dicarboxylate | 1g | 632316122 | CS-0041205 | MFCD04115344 | 278.308 | C14H18N2O4
Ambeed | 4-Nitrophenyl stearate | 1g | 552599236 | A158930 | 14617-86-8 | MFCD00047733 | 405.579 | C24H39NO4
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