According to the paper; starvation appears to be the way to go.
Lithium orotate appears to be the safest way to take a lithium salt and it is available without a prescription because of its safety.
FWIW: I have been taking lithium orotate for decades with no ill effects.
“These results are supportive of the lack of a postmarket safety signal from several decades of human consumption.”
BTW: These were rather massive doses.
I have not taken any anti-aging drugs yet. I will try 1) capers (substitute for rapamycin - has more affinity to Everolimus), 2) myricetin supplement or cranberries (trametinib substitute), and 3) lithium.
The docking studies support Kaempferol to be a potential ligand with docking score values of 33.4 (3CQU-3D structure of AKT1)] and 27.3 (2FAP-3D structure of FRB domain of mTOR) respectively as compared to that of standard drug Everolimus with 24.4 (3CQU-3D structure of AKT1) and 20.1 (2FAP-3D structure of FRB domain of mTOR) respectively. Docking studies along with ADMET results shows that Kaempferol has favorable drug likeliness properties and bind to the same active site (site1) of the targeted proteins (3CQU-3D structure of AKT1) and (2FAP-3D structure of FRB domain of mTOR) where the standard drug Everolimus is known to bind. Conclusion The study exhibited that Kaempferol was having a better binding affinity towards the receptor FKBP12, a Rapamycin Binding Domain and AKT serine/threonine-protein kinase resulting in its better efficacy in the mTORC1 inhibition as when compared with standard drug Everolimus against HCC.
Capers have the highest level of kaempferol.
It just got dried capers in salt two days ago. Rinsed them several times, to remove the salt, and soaked them overnight for good measure. Dried them in a dehydrator. Waiting for the myricetin to arrive in two days. Lithium? I am poking around to find out a suitable dosage.
I plan to take it three days a week. Most people here take rapamycin once a week. Because of the half-life, the rapa, probably stays in the body about three to four days. Myricetin has a half life of eleven hours. But kaempferol has a half life of only 3-4 hours. I have to plan a more frequent dosing, maybe BID or TID.
They got it from LC labs. It looks like Trametinib is only DMSO soluble, “ is practically insoluble in the pH range of 2 to 8 in aqueous media . MEKINIST (trametinib) tablets are supplied as 0.5-mg, 1-mg, and 2-mg tablets for oral administration. Each 0.5-mg tablet contains 0.5635 mg trametinib dimethyl sulfoxide equivalent to 0.5 mg of trametinib non-solvated parent.”
I assume the tablets wouldn’t be able to be ground up and placed in rodent chow?
No need to worry, the ITP guys can get it from a chemical supplier like Sigma-Aldrich or directly from Novartis. You can submit an application to them if you got time to spare.
If you scroll down to the bottom of the link you provided the powder still needs to be formulated with DMSO to be bioavailable I think. If they formulate with DMSO and then grind it all up into rodent chow does that work? Or does it separate it out from the DMSO? I don’t have enough of a chemistry background to know these things