C2
NPF · C26H15NO7 · MW 463.40 g/mol
A substrate and reporter group for enzymatic and bioanalytical assays. Enzyme-mediated
hydrolysis or reduction of the nitrophenyl ester bond changes absorbance and fluorescence,
producing an optical signal proportional to enzyme activity or analyte concentration.
- Enzyme activity reporter
- Esterase substrates
- Hydrolase profiling
- Plate-reader compatible
- Readout
- Absorbance · fluorescence
- Stage
- Synthesis to order
- Indicative
- Price on requestby quantity and application
C3
Pyrrolidine-based sphingolipid analogues
Synthetic compounds designed to mimic the structure and function of natural sphingolipids. The
five-membered nitrogen heterocycle improves chemical stability and affinity for specific enzymes,
making these candidates for inhibitor development and lysosomal disorder research.
- Glucosylceramide synthase inhibitors
- Gaucher disease research
- Ceramide regulation
- Anticancer screening
- Evidence
- Synthetic capability · characterisation on request
- Stage
- Synthesis to order · licensing open
- Indicative
- Price on requestby quantity and application
C4
Sphingoid bases · D/L-ribo & D/L-arabino
Natural components of plants, yeasts and human skin. Four stereoisomers differ in the spatial
arrangement of hydroxyl groups, which makes the set useful for enzyme stereoselectivity studies.
D-ribo-phytosphingosine is the most common natural form.
- Cosmetics & dermatology
- Skin barrier
- Anti-acne research
- Enzyme stereoselectivity
- Evidence
- Synthetic capability · characterisation on request
- Stage
- Synthesis to order · licensing open
- Indicative
- Price on requestby quantity and application