Saturated hydrocarbons

Medchemexpress LLC PENTADECANE-D32 50 mg

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PENTADECANE-D32 50MG

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Ambeed AMBEED

5000882545 DODECANE-112-DIOL 100G

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Ambeed AMBEED

5000884755 CYCLOHEPTANE-13-DIONE 5G

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Ambeed AMBEED

5000883742 2-METHYLCYCLOPENTANE-13- 100G

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Ambeed AMBEED

5000887637 CIS-CYCLOPENTANE-13-DIOL 250MG

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Chemscene CHEMSCENE

5000577611 CIS-CYCLOPENTANE-1 2-DICA 100G

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000757455 DIMETHYL TETRADECANE 5G

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Medchemexpress LLC TETRADECANE-1 14-DIO 50G

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TETRADECANE-1 14-DIO 50G

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Chemscene CHEMSCENE

5000576455 2 2- CYCLOPENTANE-1 1-DIYL 5G

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Chemscene CHEMSCENE

5000576358 CYCLOHEPTANE CARBOXYLIC ACI 5G

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eMolecules​ 6760-99-2 | 8-azabicyclo[3.2.1]octane hydrochloride | Pharmablock | MFCD19982561 | 147.650 | C7H14ClN | 97.000 | Cl.C1CC2CCCC1N2 | 25mg | 551186727

8-azabicyclo[3.2.1]octane hydrochloride | Pharmablock | 6760-99-2 | MFCD19982561 | 147.650 | C7H14ClN | 97.000 | Cl.C1CC2CCCC1N2 | 25mg | 551186727

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Medchemexpress LLC 18-azido-stearic acid | 1529763-58-3 | MFCD35066654 | ≥95.0% | 325.49 g/mol | C18H35N3O2 | 10 MG

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18-Azido-stearic acid is an azide-functionalized long-chain fatty acid used as a hydrophobic bioconjugation linker for click chemistry. It enables efficient attachment of lipophilic tags or cargos to biomolecules via copper-catalyzed or strain-promoted azide-alkyne cycloaddition, and is supplied as a stable powder for laboratory research use.

• Contains a terminal azide functional group for click reactions.
• Compatible with CuAAC and SPAAC bioconjugation methods.
• Hydrophobic stearic backbone facilitates membrane incorporation or lipophilic tagging.
• Solid powder form with recommended storage for long-term stability.
• Available in small milligram pack sizes suitable for research applications.

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Cambridge Isotope Laboratories n-Tetradecane (D30 98%) 1 g

n-Tetradecane (D30 98%) 1 g

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Medchemexpress LLC I-287 | 2014368-93-3 | 99.4% | 565.04 | 1 ML

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I-287 is an orally active, selective PAR2 inhibitor that acts as a negative allosteric regulator on Gαq and Gα12/13 activity and their downstream effectors. It has been shown to reduce Complete Freund's adjuvant-induced inflammation in mice and can be used for inflammation/immunology research.

• Inhibits PAR2-mediated activation of Gαq and Gα12/13
• Inhibits PAR2-mediated ERK1/2 activation in HEK293 cells
• Inhibits PAR2-induced secretion of IL-8 cytokine in HCT-116 and A549 cells
• Reduces Complete Freund's adjuvant-induced inflammation in C57BL/6J mice

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Medchemexpress LLC Hexadecane-1-thiol-d33 | 218956-22-0 | 98% | 291.71 | 1 MG

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Hexadecane-1-thiol-d33 is the deuterium labeled Hexadecane-1-thiol. Deuteration has gained attention due to its potential to affect the pharmacokinetic and metabolic profiles of drugs. Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, primarily as tracers for quantitation during the drug development process.

• This compound can be used as a tracer.
• This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.

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