Dear All,
 does anyone have any clever suggestion/s for handling the solubility problem
 of highly hydrophobic compound, during co-crystallization or inhibition
 assays? The ligands I am using are almost insoluble in aquous medium
 (precipitates out or becomes turbid at ~1 micro molar conc.). In DMSO, the
 solubility is upto 50mM. Ligands are not soluble in MeOH or EtOH.
 Besides crystallization,  this solubility is also a hindrance for
 in-vitro or in-vivo assays requiring higher conc. of ligand (keeping in
 mind, the final DMSO conc. <5%)!
 Some of the ligands have benzoic acid groups. Does it help to convert them
 to Na benzoate form?
Thanks for your time,
Tuhin.

Dept. of Physics
Indian Institute of Science.




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