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Description
Virtual compound screening in drug discovery
doi: 134
Simon et al., 1973
& Jefferies, W
Its single-ester pharmacokinetics produce more consistent and predictable hormone levels
Overall, there are no publications to suggest that the consumption of T or T 3 at conventional dietary or supplemental doses may induce the expression of hepatic efflux transporters or cause hepatic membrane-transporter-mediated drug interactions in vivo
