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doi: 10.1016/S0140-6736(20)30566-3 308 ZuoL.PratherE
Discovery of BMS-986339, a pharmacologically differentiated farnesoid X receptor agonist for the treatment of nonalcoholic steatohepatitis
It also increased acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) activity, key enzymes that modulate acetylcholine, the neurotransmitter crucial for learning and memory [1]
2
The absence of a listed interaction is not the same as proof of safety, but the pharmacokinetic analysis above explains why no interaction would be expected
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