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Patients who are homozygous or compound heterozygous for no function DPYD variants (i.e., carry two no function DPYD variants) or are compound heterozygous for a no function DPYD variant plus a decreased function DPYD variant have complete DPD deficiency and are at increased risk for acute early-onset of toxicity and serious life-threatening, or fatal adverse reactions due to increased systemic exposure to XELODA

PSPeptides offers research-grade 5-Amino-1MQ for laboratory studies investigating NNMT biology and adipocyte metabolism

It has been demonstrated to improve brain function and short-term memory in healthy older adults

FD patients as a group have comparable fasting plasma levels to those in health (95)