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The latter compound is androgenically inactive, but it is a pyrogen (e.g., a fever-producing agent) that has been associated clinically with some febrile conditions.
The latter compound was primarily distributed in the perinuclear region.
The latter compound reacts with Gibbs reactive (2,6-dibromchinon-chloramide) resulting in a blue precipitate.
A stereoselective synthesis was projected to obtain single enantiomer of the latter compound.
The latter compound represents the first example of all-carbon linked arabinofuranotriose analogue.
However, despite larger capacity, this latter compound remains to be optimized in term of cycle life.
This latter compound seems to be synthesized for the first time.
Differing from the latter, compound 2 has one more hydroxy group and a ∆15 double bond in its structure.
Preliminary clinical data on Y1-targeted tumor imaging with the latter compound in breast cancer patients are encouraging [18].
For the latter compound, DCNP depletion occurred ca. 80-fold faster than in the absence of organocatalysts.
The latter compound was subsequently deprotonated and used to polymerize ethylene oxide by a classical core-first approach.
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