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So when a product sold as CJC-1295 no-DAC is described using the Teichman half-life or IGF-1 numbers, it is borrowing data from a different molecule with a fundamentally different pharmacokinetic profile

For instance, in M1 pro-inflammatory macrophages (Ms), there is a metabolic break at isocitrate dehydrogenase in the TCA cycle due to suppression of its mRNA expression, leading to the accumulation of citrate and itaconate, which drive lipid synthesis and stabilization of anti-inflammatory transcription factors, such as nuclear factor-erythroid factor 2-related factor 2 (NRF2) and activating transcription factor 3 ( Unlike nicotinamide adenine dinucleotide (NAD + ), nicotinamide adenine dinucleotide phosphate (NADP + ) has an additional phosphate on the 2 position of the ribose ring that attaches to an adenine moiety and has a lower intracellular concentration than NAD + ( Figure 1A )

Its going to be a tough sell both to consumers and to pharma partners

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