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Theoretically possible but extremely unlikely

It has been reported that BHBA can regulate BDNF transcription by affecting epigenetic modifications, such as increasing the occupancy of the transcriptional activation mark H3K27 acetylation and decreasing that of the transcriptional repression mark H3K27me3 at Bdnf promoters ( Bdnf promoters II and VI in the hippocampal neuron line HT22 ( Bdnf promoters I, II, IV, and VI were also increased after BHBA treatment, indicating that H3K4me3 is involved in the increase of Bdnf expression in response to BHBA stimulations, possibly acting cooperatively with H3K27me3

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Ansamycin derivatives such as 17-AAG (tanespimycin) and 17-DMAG (alvespimycin) reduce tau and -synuclein oligomerization in AD and PD models by promoting their degradation via the ubiquitinproteasome system

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