gem-Difluorinated Amines for Drug Design
Fluorinated derivatives play an important role in medicinal chemistry. The selective incorporation of a fluoroalkyl group into bioactive compounds often affects their binding affinity, metabolic stability, lipophilicity, membrane permeability and bioactivity. gem-difluoromethylene group (CF2) is a valuable fluorinated motif that is present in pharmaceuticals and biologically active compounds. In particular, gem-CF2-group improves ADME- and PK-properties. In this context, Enamine offers a library of unique difluoro-substituted cyclic amines for drug design.
Concept
We offer:
>100 gem-difluorinated amines on gram-scale from stock.
MedChem Highlights
- Aliphatic Trifluoroborates (-BF3) for C-C couplings
- Functionalized Vinyl Boronates for C-C couplings
- Unique 3D-shaped Spirocycles
- Water-soluble non-classical benzene mimics
- gem-Difluorinated Amines for Drug Design
- Fluorosulfates and Sulfamoyl Fluorides
- Alkyne-containing Linkers
- Structurally optimized tetrazines for rapid biological labeling
- Building blocks and linkers for PROTAC synthesis
- Heterocyclic Sulfonyl Fluorides
- Silicon-Containing Building Blocks
- Epoxides for Drug Design
- Analogues of CF3-Pyridine for Drug Design
- Piperazine Bioisosteres for Drug Design
- Sugar-like Building Blocks for Drug Design
- Cyclic Sulfonamides for Drug Design
- Morpholine Bioisosteres for Drug Design
- P(O)Me2-containing Building Blocks
- Saturated Bioisosteres of ortho-/meta-substituted Benzenes
- Saturated bioisosteres of para-substituted benzenes
- Sulfonyl fluorides (-SO2F)
- Diazirines
- Oxetane-containing Building Blocks
- SF5-Building Blocks
- Stannanes for coupling reactions
- Sulfoximines for Drug Design
- Heterocyclic scaffolds
- Azide-linkers for Drug Design
- Unnatural Amino Acids
- Cubane-containing building blocks
- Benzoxaboroles for Drug Design