Senolytic compounds and compositions
preclinicaldrug program · medium · Thu Oct 19 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Create selective senolytic agents suitable for anti-aging applications by targeting senescent cells.
Patent-covered compositions including senolytic agents; the record references magnolol and formulations for oral, topical, or transdermal administration.
US patent application published and listed as pending.
Compositions that protect cells from oxidative and mitochondrial stress
discontinuedother · medium · Thu Jan 16 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
Mitigate effects of aging by enhancing cellular resistance to DNA damage, oxidative stress, and mitochondrial stress.
Patent-covered compositions for oral, topical, or transdermal application intended to protect cells from oxidative and mitochondrial stress.
PCT patent publication listed as ceased.
Nuchido TIME+
undisclosedconsumer product · high
Increase NAD+ and support healthy aging, cellular health, energy, vitality, performance, recovery, inflammation, sleep quality, and brain fog.
Dietary NAD+ boosting supplement developed using a systems-based approach targeting multiple points in the NAD+ salvage pathway; evaluated in a double-blind, randomised, crossover human trial.
Published human trial evidence showing Nuchido TIME+ increased whole-blood NAD+ and affected biomarkers associated with healthier aging.
Increased NAD+ concentration in whole blood; associated with increased SIRT1 and NAMPT in peripheral blood mononucleocytes, lower pro-inflammatory cytokines including IL2, reduced glycated serum protein, and IgG glycosylation shifted toward a younger biological age.
Systems approach to NAD+ restoration
exploratoryresearch program · medium
Develop more reliable interventions to restore NAD+ by addressing biological complexity behind age-related NAD+ decline.
Research program proposing multi-node targeting of the NAD+ interactome rather than single-target NAD+ precursor supplementation.
Published review and rationale for a systems approach to NAD+ restoration.
The publication argues that variability in NAD+ supplement efficacy may result from single-target approaches and that targeting multiple key nodes in the NAD+ interactome is likely to be more efficacious and reliable.