A wellness and youthification drug, and longevity drug could be producible at when Adenosine, the amino acid, at a new drug form where the adenosine is linked to a membrane transport molecule or protein, could possibly increase the amount of adenosine triphosphate that gets made because there is more substrate adenosine at the cytoplasm to enhance with PO4 groups. One possibility is chlorophenoxy adenosine, the chlorophenoxy group gets it past membranes, then it is available adenosine at cytes; I perceive I read that lipophilic molecules have better trasnport past the blood brain barrier, so as those are cytomembranes that get passed, it is possible that a lipophilic variation of adensine could be an ATP heightening supplement. You might just be able to put a /\/\/\/\/\ alkane tail on the adenosine, possibly detachable and at the same molecular location the PO4 attaches to at ATP; it is possible an adenosine-O-/\/\/\/\/\ where an oxygen links to the alkane would still be lipophilic enough to pass the cytomemebrane while the oxygen linker makes it easy for the cyte to metabolize into available adenosine (and the “extra” lipophilic alkane part); another possible cytomembrane passing adenosine molecule is a branched phosphoalkane (like a phosphorus clover, but with methyls or ethyls instead of Os at a PO4 shape).

At adensosine/\/\/\, I do not know how big that alkane has to be to be lipophilic, it is possible, besides an alkane, or branched very mulimethyly alkane, that a lipophilic keytone could provide enough lipophilicity to get the adenosine past the cytomembrane while being harmless when the ATP supplement is converted to adenosine (and thus ATP) as well as the extra molecule parts that are at the cytosol, at doses that imaginably 100 mg to grams a day of supplement. If there are any ketones that are good for people, then those might be beneficial moeities for the adenosine. The other thing I have perceived is that butyls are sort of harmless or beneficial, I have vague memories of circulating butryate being beneficial soperhaps the adenosine/\/\/\/\ could be a butyl, or a branched butyl.

The thing to make a cytosol ATP-available amount increasing supplement with depends on if the phosphorylator reaction chemicals are replete with lots of PO4, and could use more adenosine. If alternatively, they could use more PO4, then PO4 linked to a membrane transport chemical, like something lipophilic, or a peptide or protein could bring PO4 to the cyte, heightening the amount of PO4 available for cycling and recycling at the ADP->ATP cytoprocess; another approach would be to increase P phosphorus recycling at the body, at the cyte and cytoplasm, it is possible there is some sort of phophorous export channel that a drug could downregulate, or possibly heightening the amount of, or upregulating an enzyme that turns phosphorus containing proteins that get recycled or other phosphorus containing stuff, so that there is more available phosphorus to make PO4 from. Another actual amount of ATP at the cytological ADP->ATP available chemical pool raising drug or supplement could be a drug that caused people to only pee out 1/4 to 1/2 as much phosphorus then this could be measured as to if it increased the amount of functioning ATP, or if mice meaured throughout their lives have longer healthspan and greater lifespan from having more ATP, longer, than other mice.

I read 90 lbs of ADP gets turned into ATP each 24 hours, so it is possible that the thing that affects the amount of ATP available at the cyte and cytoplasm is actually the amount of adenosine, as the phosphorylation looks highly available at 90 pounds every 24 hours.

Longevity genes and drugs: different cytes hve different numbers of mitochondria, do existing SNPs of well humans cause different higher amounts of mitochondria at particulr cytotypes. Imaginably leukocytes have 200 mitochondria each, but hepatocytes have 700. Are there naturally occuring genes or SNPs (single nucleotide polymoprhisms) that cause a leukocyte to have 700 mitochondria or a then noting that at those gene variants or SNPs, that a 60% decline of mitochondria number across the lifespan just moves a leukocyte to 200 from 320 mitochondria per cyte, or a hepatocyte to 700 from 1120 mitochondria, or any kind of body cyte or tissue’s mitochondria to the average of that of a gentically pre-optimized person.

Photoactive chemotherapy is described at published literature, and lithotripsy of solid objects at the body is published. It is possible that the double slit/binomat local area bandpass energy or also chemical filter could have local tissue applications as well.

I should think of a pill that cures cancer at the developing world, like a tissue localized chemotherapeutic with really minimal side effects, or a precancer senolytic like chemical that only concentrates at cytes that are precanecrous.

Similarly, it is possible that loading up the cytoplasm with alpha-helice (or better) constructed bandpass binomats, which unless they bioconcentrate in some way automatically (they might, or could be engineerable to custom concentrate kind of like mitochondria or also membranes concentrate chemical colors); If the bandpass binomats do not bioconcentrate then even as diffuse molecules they might have some engineerable effect as cytoplasm thickeners, “modelling with percolation theory new cytoplasm chemicals” which might then also be new drugs

If increasing or decreasing the fluidity of the cytoplasm 20-40% causes some beneficial effect then along with binomat drugs as well as drugs that have effects modellable with percolation theory, are producible. Increasing or decreasing the fluidity of the cytoplasm can also be accomplished with gene therapy. Looking at the wellness and lonvevity of people with differing cytoplasmic fluidity or also cyte as gel-bag stands up from viscosity morphology, and osmotic profile measurables produces data that can be used to find indications of use, and effects of new fluidity/viscosity/osmotics drugs..

As a beauty drug,
lyse a radiolabelled cyte, then put the goop outside the cytomembrane of a well dermatocyte, then find out which specific chemicals at cytoplasm are able to migrate into a cyte. It is possible some of those chemicals, which can be taken up adermatocyte from topical application, are easy and simple to produce. These new membrane-passing fluidity/viscosity/osmological chemicals are topically active things that cause the gel-bag perspective firmness of hydrated skin, and with the gel-bag perspective of cytomorphology have the same gel-bag standupness, whihc possibly causes youthful morphology like youthful skin.

GSK, online content So, find out what at just released cytoplasm will pass the cytomembrane of a well cyte, then make a big list of those chemicals, any of theose chemicals that do something could be new drugs that easily pass the cytomembrane, also new molecular variants on those cytomembrane passing naturally occuring chemicals could be new drugs. Even cytochemicals without an obvious drug effect like cytoplasm thickeners (imaginably NaPCA like proteins) could be used as tissue firming, youthful morphology producing ingredients that are actually absorbed and utilized from topical application..

and possibly also cause the dermatocytes to be bnearer their younger shape, that is morphology.

The production of hyalonuric acid and collagen at dermatocytes is, I perceive, chemicals actually at the cytoplasm of dermatocytes changing stiffness, osmological things, and cytoplasms gelness, conriuting to well tissue. So cytoplasm thickeners and thinners measured as to their longevity and wellness effects could be beneficial new drugs. biological systems where viscosity of cytoplasm has beneficial aspects like dermis exist, so optimizing that viscosity, osmologicalness, and morphology effecting gel-bag function could be a new kind of beneficial drugs.

Actin/tubulin amplifiers, possibly (deuterated actin might be a gradualized motion track, modified actin protein, possibly even a new SNP could make fast travel actin, each of the fast and gradual versions could be measured as to effect on wellness and longevity.

GSK, drug localization and Math: If there is an effect with the double slit stripes being taller than the laser dot, while being narrower, there might be some kind of math or physics relation where if you measure one well, the other measurement beceomes less efffective (atom electron position or velocity as measurable thing), or if there is another, different photonic system where: “if it thinks it can’t go littler it can still make x and y directions different sizes, but equationally resolved to be ok, such that one math/physics funtional measurable, like height, is much larger than another measurable like width” That causes the technology opportunity of making a beam system where if you cannot tell how tall it is, it gets to be arbitrarily skinny? Just thinking if this is a known supported math or physics phenomena, where one characteristic of a thing observable at a high resolution makes the other less observable so the system observability amount remains constant (kind of reminded of position and velocity at atoms and electrons); the idea is that you then take one of these “high resolution at one spatial axis if you skip measuring the rest” math or physics equation relationship function effects, and then build a localization beam out of it, so that way as compared with a laser dot, a cofocalization, or even a venn diagram overlap, you can make a crosshairs, sort of like one double slit “|||||||||” output layered on another “=“ to produce really optimized as tiny areas to localize the beam effect with. So that double slit crosshairs (or similar better approach) is a way to make acoustically activateable drugs, or also photonically activateable drugs have even higher addressible spatial resolution at human tissue.

If tissue has a Kerr effect, then electrically, or electric field (EM field) stimulated tissue could have a gradient refractive index (GRIN) lens effect, focusing light at the interior of the tissue.

So, doing two separate double slit like beams at 90 degrees makes a crosshairs, and the overlap of the crosshairs has more photon (or acoustic wave) energy than the rest of the lines thing is an invention; then making a material with double slit tesseleated repeat or at a biological system or polymer: a protein-based undulating landscape, like a screen of holes, could be used to produce a “interference lines are skinnier than the illuminating laser beam diameter” effect. So a purposed 2d or 3d landscape of crosshairs of heightened narrowness is produced. Tht is beneficial to localization of drug activity when the drug is activated with a beam or field like light or acoustics.

like branched amino acid polymers (noting photo, physical chemistry, or acoustically driven electret, PVDF-like, overlain layers of branches, as well as, I think other things)

can you use pulse sequence build up to

Different than a DNA machine, think of a board with three plates on it.

also, inevitable, a computer, three things seperately addressable at one molecule and considered at one molecule can make :AND, OR, NOT

This might work at diodes and CCD functional aminoacids polymers (and other biopolymers)

Thinking about the effects of a voltage doubler at a PVDF like drug molecule that either has a localization activator (like an acoustic beam some photons, or a physical chemistry thing like warmth, cool, or bending), do you get all the chemical effect from half the physical chemistry bending/molecule motion? Does a frequency doubling diode bridge cause the chemical system to be responsive twice as quickly or twice as often? Can you use diodes to make a frequency halving circuit to make a molecule responsive to higher frequencies of potential input?

Does having a bunch of diodes at a dendritic PVDF-like polymer Among many possibilities are new kinds of sensor molecules at new drugs, like a sonic, physical chemistry-effect, photonic, electric,

An amino acid that can double voltage; charge cascades at biopolymers or even things like polychrolorophyll to my perception cause a pile of electrons, that is a current. Heightening the voltage also has atechnological value.. I do not know how a diode voltage doubler works, but unidirectional charge flow in a branched polypeptide or protein seems possible. Physically I am reminded of the tesla valve as well. Then there are also possibilities like a photon frequency doubling crystal could be made out of amino acids, or possibly other biomolecules, to cause something like photosynthesis at chlorophyll to emit higher voltage to begin with.

Wikipedia notes how diode bridges double frequency, to double the frequency of a photon effect at something like polychrolophyll, or possibly make a diode voltage doubler, it seems possible to make a diode bridge out of amino acids, Online it says a diode can be made with 11 BP DNA, so with even fewer atoms at a polypeptide (11 suggests further engineerability: imagine a quatrapeptide or decapeptide that could be a diode, then 4 of them at a fequency doubling diode bridge, then arranged at a layered branching thing) a diode (and diode voltage doubler and diode bridge) might be constructible from amino acids alone, other biopolymers, or even something like a boron polymer.

or possibly some other biopolymer like PVDF-like or electret polyhydroxyapatite, cellulose, or even nonorganic Boron polymers, also chitin, or proteins; amino acids have better engineering size and particularly high ease of making; a diode bridge made out of something like

optical isomers might be a basis for making diode bridges out of biopolymers, carbohydrates are well known to rotate light a certain amount, or a diffrent amount, or I think not to, based on the chirality of the molecule like a sugar molecule. Although that is not an antireflectance coating, it is a biopolymer optical effect that might have utility

perhaps 4 antireflection coatings on a piece of optics will actually double the frequency of the light; on absorption that would heighten the voltage of a photoelectric material like chlorophyll
electric eels manage to heighten voltage, perhaps hundreds of times more than ionic voltage difference between electriceelcytes.

Doubling frequency with something very simple: https://en.wikipedia.org/wiki/Diode_bridge ”With AC input, the output of a diode bridge (called a full-wave rectifier for this purpose; there is also half-wave rectification, which does not use a diode bridge) is polarized pulsating non-sinusoidal voltage of the same amplitude but twice the frequency of the input.” So apparently 4 one way thingies at a diamond topology can double frequency when the feeding wave has a frequency to start with.

Things that might function as a photon or EM diode to build a diode bridge frequency doubler from: funky layers (thinking of metal as 180 degree photon EM field reemitter, then modify it to have directionality so that if something meets it head on, it is absent the ability, because of the funky layering, to do a 360 degree (kind of like 180 degree) reflectance reemission; My perception is that antireflection coatings (green look lenses) of a particular thickness work this way; perhaps 4 antireflection coatings on a piece of optics will actually double the frequency of the light; on absorption that would heighten the voltage of a photoelectric material like chlorophyll or a photovoltaic.

something like an antireflective coating that does its thing at 90 degrees might be both impressive and extra-functional at diode-bridge-like freqency doubling and photonic path making; four of 90 degree effectives at the corners looks a lot like the diode DC from AC maker that doubles frequency.

..5b What is an electrical Moire? layeres broomlike trees, or volleyball-net like netting, with a charge locationality and predictability. What is the meaning when you stack them on each other to moire them (sparse moire effect; neural netowrk effect from sparse moire does neural netowrk things at amino-acid sized structure, which are kind of like numerically weightable, if integers as liked, layers. Reminds me of stacks of graphene

A new chemical could exist: a piezoelectric peptide, or possibly protein. This has greater technological function as a piezoelectric peptide sequence, possibly engineered as a branching peptide (or protein), that just tends to hang out in layered, overlayering bunches, with a lots of moveable, releasable electric charge (possibly from, sound or motion, chemicals, light, chemocontact (put it next to metal it wigs out) (put it next to something hydrophilic or hydrophobic and it wigs out)

two electron (or multi-photon, multi electron, or other multi-charge causers like acoustic PVDF-like effect, or even (uh-oh it’s just a battery) ion proximity, molecule effects, noting things like ATP and phosphate groups, to my perception many many nonionic chemical systems, like ATP, GTP, and proteins are published )

systems like chlorophyll polymers with the right branching to channel a bunch of electrons towards a particular area or part of the polychrolophyll (or polychlorophyll-like) molecule.

the more things like sonic energy, drug effects, or ; with science can anything in nature be found that has a multiantenna/sensor radio telescope array like effect? Building this on purpose out of protein produces a genetically engineerable basis for new sensors at organisms, including electrical, radio, sonic, new kinds of light, THz waves, microwaves, and other frequencies
CCD protein arrays

With less utility than drugs and chemicals attached to sonic antenna molecules or polymer macromolecule antennas is acoustically activatable eentsy fluid/gel/powder beads, where the outer polymer cover or possibly lipid membrane becomes hyperpermeable or dissolves with acoustic activity like a cofocalized beam at depth in the body, or a near-surface-of-body treatment from noncofocailized, possibly even a spread area, purposefully large area, sonic beam. That activate, whether from dissolved or permeant release, or from PVDF-like surface charge effects from the sonic waves at the beads’ antenna frequency. I like the PVDF-like charge effect at keratin and chitin linked to chemicals and drugs technology more.

With localization possibly with sonic activable drugs, drugs that benefit the fetus, like gene therapy drugs, which when injected could be made to only activate at fetal tissue, which heightens and enhancing the genetics of the baby, is from localization is without risk, or many orders of magnitude reduced risk of nonintended effects on the mother.

The SNPs on the genes of the production of the produced-at-a-human amino acids would have different, and thus optimizable specifiablity at the human genome. It is even possible that the different SNPs of genes humans use to make amino acids has an intelligence:g effect, thus some variations on amino acid production genes could heighten intelligence. A variety of SNPs at amino acid production could also be wellness healthspan genes.

There a a variety of supplements, incresing the use of supplements at the population would have a numerically beneficial effect, so what would cause people to aquire supplements more frequently?

curcurmin makes wound healing more rapid, curcurmin soaked bandages and band-aids could be beneficial. Topical Curcurmin after laser or other skin outer surface layer treatments could be beneficial, but it might not, either rapidity, detailed thoroughness perhaps achievable gradually, normal healing velocity, or with more rapid healing.

Curcurmin could benefit beautification effects of laser skin treatments and other beauty treatments modify the skin or dermis (lasers, chemical peels, sonication, or combinations where something like a beauty peptide, at 2019 AD some were tripeptides or other peptides with less than 10 mino acids) or NMN, combined with a wound healer, causes a simultaneous or near simultaneous multipart effect of dermatocyte proliferation with mitochondrial improvement, greater histonation for higher fidelity protein and cytostucture production, or heightened cytochemical optimization like more collagen or more hyalonicuric acid at part of the cytocontents.

technologies that treat, prevent, cure and or also diagnose cancer ultraffordably (cheaply) notably at the developing world, where the technologies are also functional at the developed world:

perfumed antibody that are an an enteric pill or a snortable cheap think like a drink mix stick pak: 16 for 1$, so 7 cents a snort.

A "fizzy tic tac" is a tic-tac sized diagnostic pill shaped thing that you can put in a container of pee. The idea is that it is a cheap to make as a tic-tac or possibly cheaper. The oter layer has a nonreactive coating, and just underneath it is a layer that fizzes to dissollve like sodium bicarbonate and a harmless organic or polyprotic acid that dissolves away a coating layer to reveal the imunno color changing stripe, shape, or stripes printed on an inner surface.
A "perfumed antibody" is an antibody attached to a chemical that has unique high detetability at minimal solute amount at another antibody test such as a circulatory fluid or pee immunochemical test like the ones in dollar store pregnancy tests; this test would also have higher resolvability with greater ability to distinguish between what I describe as "perfumes" when mentioning the different chemicals. One kind of perfumed antibody could be a unique polypeptide or even artifical amino acid peptide that is linked to the antibody that gloms biologically available chemicals or even biostructures; the perfumed antibody might work even better at seperating when glommed from having an enzymatically degradable linker molecule between the antibody and the perfume, one possible version is antibody:ATP:perfume where the ATP, or one of its phosphates pops off when the antibody gloms onto something.

hyperaffordable antibody tests for cancer (or heart disease) based on $1 dollar store pregnancy test; pregnancy test has three lines, about 7 mm tall. If only one of the lines has antibody-reactive colorant at it then an antibody test with a 1 mm indicator view can be seven times cheaper, or 15 cents a test, more niftier is the version if all three lines at a dollar store pregnancy test are immunoreactive colorized; then there are 21 linear mm of antibody indicator material, which produces 21 cancer antibody tests per dollar, or about 5 cents a cancer diagnostic test.

personality test

perfumed antibodies liberate the perfume when they glom, and then the perfume, which might be linked to, or part of, a molecule that heightens excretion at the kidneys, is particularly easy and accurate to detect at an antibody pee test. So if an antibody gloms to a acancer site at any place in the body the antibody releases the perfume, which shows up at the antibody pee test; noting the math of false positives

senolytic cancer chemotherapeutics cause an effect where even if you get a flase positive (developing, if you test positive fr cancer, just take the senolytic chemotherapy pills; the cancers being tested for are preferentially, or only the kind that can be cured with pills, so the ill person gets to skip the doctor, the hospital, and skip the costs, just getting the pee test and the senolytic optimized chemotherapy pills. Becasue the chemotherapeutic drug is also a senolytic if you take it for 2 or 3 weeks with a false positive diagnoses, then the senolytic function mkaes you live years longer and be weller anyway, and of course for some that test positive it cures their cancer.

si rna

siRNA or other RNA drugs, like cancer treating or curing chemotherapeutic drugs can be structured to last longer or less long at the circulatory system, it seems possible that a chemotherapy drug that just lasts 45-120 minutes could terminate oncocytes rapidly instead of gradually, and only be felt as a chemotherapeutic experieince for a few minutes; that brings up the opportunity to have a comuter linked to an automatic dosing machine, even one at the person’s dwelling, figure out when the person was completely asleep, in deep sleep, and likely to keep sleeping; then the dosing machine would dose the person with the siRNA or other RNA drug, and all of the acute feelings from the chemotherapy drug would go unexperienced, and the person would feel ok instead; there is a version of this that is better than dosing while asleep: doctors or online software or phone apps could give people a psychiatry quiz or survey that then estimates, at 95% likelihood or higher, that they have a nonaddictive personality. If they have only a 1 per 20 or less chance of craving a euphoria inducing drug or chemical after they end treatment then the patieint can be given MDMA or benzodiazepenes to take for the duration of the siRNA (or other RNA drug)’s duration of action. The person experieincing chemotherapy would feel wonderful.

It is possible there are senolytic siRNA or RNA drugs, if so, some variations on those siRNA or other RNA senolytics could be modified to there is[anticancer|senolytic] physical structure possible at liniear si RNA or other RNA drugs, and at branched siRNA or RNA drugs then the branches can each have a different drug effect at that branches RNA, so perhaps a ratio of three senolytic RNA branches to one highly effective antioncocyte RNA branch; thats a way to tune the senolyticness and anticancerness of the siRNA or other RNA drug.

oncocytecytoreproduction disrupting IPMAT active siRNA or other RNA drugs could disrupt the cytoreproductive cycle, affecting dividing oncocytes more than well tissue
pure siRNA or RNA drugs could be produced at yeast, bacteria, or plants making them decentralized and ultraffordable at the developing owrld.

Cheap, easy to make chemicals approximate the anticancer effects of fluorouracil: wobble uracil; Mg,Ca, Sr, Ag, P uracil versions where the uracil molecules contain a Mg or Ca, or Ag or P atom. Some of the atoms are +2 or -2 electrons so the modified uracil might come as a two-uracil, one Mg or one Ag dimer, or you could just stick a hydrogen on it or something to make a nonionizing water soluble molecule. Notably magnesium aspartate and magnesium threonate exist, and that is an amino acid linked to a magnesium, magnesium threonate crosses the blood brain barrier to be a beneficial nootropic, so MgUracil could be functional at passing the cytomembrane of oncocytes.

along with uracil, anticancer drugs could also be based on the other RNA amino acids, adenine, cytosine, and guanine. So wobble or extra atom versions of any of these could be anticancer drugs.
Ag uracil might be cytotoxic as when the uracil is incorporated into the oncocytes RNA the metal ion at the amino acid completely modifies the shape of any polypeptide, ribosome, or transcription string it is part of, a little like having a halogen atom (like at fluorourcil) disrupt all kinds of cytothings, only with a metal atom that is very cheap to mass produce. There is the possibility that things like Mg-uracil could be produced at bacteria that just had lots of Mg at their growth media, something that would not likely work with halogen atoms.

wobble uracil is where a ultraffordable source of uracil, like a yeast or bacteria, even a modified beverage yeast, has a variety of constructor enzymes and other proteins that direct the assembly of the actual uracil molecule; then those constructor enzymes or proteins’ genes are genetically modified so the constructor enzymes work a little differently, perhaps causing them to do different things like put an extra NH2 on the cyclic part of uracil, or perhaps put an -OH where a =O is on uracil. Possibly wobble uracil does something with novel chemical structure, like putting a P phosphorus on the uracil, or possibly making a multicycle (<=><=>) molecule; so the wobble uracil makes any kind of uracil chemical variant that it actually does from modifications to the genes at the uracil production enzymes, then noting the product developer already has a genetic system that produces it, those nmerous wobble-produced versions of uracil are measured as to their anticancer effects. Perhps the PO4 or PNOH uracil is stable enough to be incorporated into nucelic acid replication structures at the oncocytes but is so novelly HOMO shaped as to halt cytoreproduction of oncocytes. a 1000 times 1000 grid of tissue culture of well tissue cytes and oncocytes could test an actual million variants on the uracil molecule for anti-cancer effects at just one testing plate. It might be possible, and complementary to planned variations on consructor enzymes, to mutate several thousand versions of uracil constructing enzymes on a plate, in place, and then test their output right on the same spot with autopipetted or possibly sliced cheese-overlay on a waffle maker, then clamped to make a whole bunch of array elements, each with its own blob of cheese, so a clamped grid with a sheet of oncocyte tissue culture tissue clamped at it to make an array, could produce a million sample areas of tissue culture tissue at a 1000 times 1000 grid plate. So, clamping the tissue with the waffle maker, would place the tissue above the microwell sample of bacteria with wobbly enzyme gene variations that produce a million different variations on the uracil molecule, the two of them combined test each uracil molecule variant with an oncocyte tissue culture mini-blob to effect.

phenylalanine production at yeast, bacteria, or plants as source of the phenyl group to produce enjoyable phenyl<alkane>amines at with biological systems like plants, yeast and yogurt bacteria. Phenylethylamine is different than the chemical produced but it is one of many stimulating, nootropic, near-euphoria producing chemicals that I perceive can be made, and have been published, that arise from a phenyl, and an amino group at the same molecule. This phenyl amino chemical makes people actually like and enjoy the experience of the beverage, yogurt or plant. With an optimal phenyl<chemical>amine the experience could be much better than tea and a really beneficial experience that was physiologically harmless.

and uracil dimers that function a lot like fluorouracil but are particularly chep to make, wobble uracil might be easily and cheaply produced at yeast or bacteria or plants, that means than a cancer treating fermented beverage, yogurt, or vegetation plant can be produced on demand, without central authority, and ultraffordably at the developing world.

rapamycin, the chemotherapeutic molecule, slightly modified to be a senolytically effective version of the rapamycin chemotherapy drug. That way if you get a false positive on a cancer test, and take senolytic-rapamycin for 10 weeks your lifespan and healthspan go way up. based on the name -mycin it is possible rapamycin started out as a fungi product, if so, perhaps senolytic rapamycin could be engineered to be produced at yeast or bacteria so is available as decentralized, autorenewing longevity and wellness senolytic drug that treats or cures cancer;

one of the things about the perfumed antibody pee test for cancer is that a math structure where if the detection rate finds one cancer in 10,000 concerned persons, and one false positive in 5,000 concerned persons, the likelihood that he cancer test actually found cancer is only 1 in three; so the math of the part where treatment with a senolytic longevity and healthspan enhancing drug that also happens to be an anti-cancer chemotherapeutic drug causes decades of greater longevity and healthspan at a well person and saves decades of living at each person when the drug effectively treats or cures the cancer; that makes treating a false positive, without using any followup tests or even medical practicioner visits, net beneficial to each individual, and more net beneficial to the group as a whole. The nonoptimal part of course is that the person spends 10 weeks on rapamycin or dasimutib or someother chemotherapy drug, and likely feeling nonptimal while they are on it. So, at the developing world, they could use senolytic anticancer drugs and skip actual visits to medical practicioners, further tests, imaging, and hospital stays; notably though, the cancer tests could only test for those cancers with a 90% pills-only cure rate. So if cancer were detected with a 2.5 cent pee test, 9 out of 10 could be cured with just pills, and if the confirmationless test was a false positive the longevizing and healthspan of the senolytic anticancer drugs would cause net benefit to the treated person.

At the developing world, aligning promoted, automatic tests around things that have ultraffordable treatments could be a group longevity and wellness optimizing strategy; if social and fiscal resources could only cover a part of testing and treatment at all the possible illnesses that might occur at the developing world.

dasimutib, molecularly modified to treat and cure the most curable cancers, that the perfumed antibody cancer tests looks for; dasimutib, or the actual name of the d-something-ib senolytic drug that is also a chemotherapy drug. It makes mice live longer from the senolytic effect. Modifying name-like-dasimutib (tested with quercetain)(called DQ here) anticancer senolytic to be effective at treating breast cancer causes a numeric effect where DQ causes such a number of increased person-years of living

tamoxifen molecularly modified to be a longevity and healthspan increasing senolytic; notably wikipedia says tamoxifen is produced now with either yeast or bacteria at bioreactors, so a beverage yeast or yogurt bacteria source is a technology beneficial at the developing world, decentralized and ultraffordable technology, that is apparently a slight modification of what already exists.

aminocurcurmin, curcurmin is like a 50% active senolytic at a graph I saw, so a modification to the curcurmin molecule could produce an anticancer chemotherapeutic drug. An ultraffordbale version produced at a plant or yeast might be possible as curcurmin is already a plant product; as a plant product it is possible that even a modified curcurmin, like an aminocurcurmin, where the amino group placed on the curcurmin, or some peptide or protein on the curcurmin causes it to be actively transported across the cytomembrane causing oncocytes to gather it.

perfumed antibodies increase sensitivity, resolution, and the number of chemicals that an immunochemical pee test can respond to

gel capsules are perhaps less than 1 cent, noting fiber optic magnifying a color, It seems possible that a particular shape of gel could magnify a 1mm sized immunodot, noting there are 21 of them at a three line imunnochemical pregnancy test to make them 5c and 1c gel magnifier

a new to me immunochemical diagnostic, like a dollar storepregnancy test, would be breathing out at a microstraw or regular sized straw so that moisture condenses, then having the immunochemical color shift chemical react to the exhaled condensate. I have no idea what biochemicals concentrate at breath condensate, but they could make a list of all of them, and any that predicted or indicated wellness or illness could be the basis of useful antibody-color shift diagnostics. I perceive beverage stirring microstraws might be less than 1 c each. the part where immunochemicals are printed, or rinsed through, the interior of the microstraw is one thing; It is possible that coating the microstraw (or full sized straw) with a deliquescent material that liquefies when breath is breathed on it could make the immunochemical much more rapid to react, and able to react with less human moments spent blowing on the straw. Another possibility is that or, possibly NaPCA combined with a acylamide gel, to make a fast inflating liquid gel reservoir with color change indicator at it, possibly making positioning of a “readout line” from a particular viewing angle, possibly near a part of the microstraw that had a lensish blob of plastic near the gel blob; that way the more regular environment and structure of the NaPCA with polyacrilimide gel blob causes more predictable reactivity, and lens-located readability than colored NaPCA syrup would; also the gel blob technology could be near 1c as the amount of immunochemical could be much less than the amount required to make an NaPCA syrup turn color enough to see. (although the microstraw might be another 1c) Also, with a condensate immunoscreening straw, the autohydrating gel blobs could be at a linear or geometric array, and each blob at the arrary could report on the immunodetection of a different chemical. Although it could be possible to heap up or multiplex some immunodetected chemicals to provide benefit, for example, 10 immunochemical responses that test fro cancer could all heap into one gel blob at a line or geometry of 7 or 20. If that one gel blob is nontransparent then perhaps there is a 1/3 or 2/3 chance the sample provider, who breathed into the straw

comparing immunoscreening the entire volume of a few liters of comparatively concentrated circulatory fluid with the few hundred ml of pee at a pee test, the number of different chemical-form or cytosurface things that can be antibody-glommed is possibly tens of thousands of times to millions of times higher as to the number of available chemicals and outer cytostructure to a immonodiagnosis from, that means the diagnostic is much better at finding disease, or even finding wellness. Also, as the perfumed antibodies release the perfume, which is another way of saying the chemically unique, high affinity, possibly linked to a molecule that the kidney preferentially excretes, reporter chemical (possibly a uniquely sequentially coded peptide or biopolymer, the production of the peptide or biopolymer sequences could be automated so that they are automatically produced in peptide codes for digits 0 to 1 or 2,000) that is excreted at pee; Then when the person puts the

fizzy tic-tac or microcoated aspirin at 2 c to less than 1 c each. They turn blue to communicate that cancer chemicals were detected,notably at cancers that are very easy and affordable to cure.

Minimizing false positives at a cancer test: multiple simultaneous immunoactive diagnostic antibodies: find (immunodetect) say three chemicals, each a separate independent indicator of cancer, although the false positive might be 1 per 1000, three chemicals have a combined preence false positive of 1 per billion. such as perfume from perfumed antibodies, but it could just be nonperfumed naturally occuring cancer predictive chemicals at pee. Also, although it seems possible to come up with a different system, an immunochemical pee test, similar to a dollar store pregnancy test, could have histograms made from antibody-color bar segments. If the cancer bar was three rectangles high then it is the one false positive in a billion, three antibody simultaneous response. If the cancer histogram bar is only one rectangle high it might just mean “think” or perhaps, “senolytics make you live longer and be weller, the cancer being tested for has a 95% cure rate from oral chemotherapy alone, so you are in great shape if you just get the chemotherapy pills and take them” Then because the test makers and distributors have structured the antibody tests to find cancers that have high treatability, the person can have a medically beneficial, senolytic, lifespan heightening cancer treatment that cures 95% of cancers of their tested type without further medical assistance, imaging, hospitalization or even physician contact. That makes cancer treatment, of cancers that can be successfully be treated, much more affordable and also more widely treated at the developing world.

Depending on how you look at the numbers, an oral perfumed antibody pill could be as little as 5 C Online, one gram of various antibodies at bulk is $573, and imaginably, 100 nanograms could be a perfume antibody dose for glomming of just one chemical. So that makes a 100 chemical diagnostic amplifying pill with 10 micrograms of antibodies, so at 100K doses per $573, the amount of C on the antibodies at each perfumed antibody pill is about one half cent per pill. Now the way the perfumed antibodies are linked to ATP and have a numeric-like biopolymer antigen for the pee test to respond to goes with a 10 or 20 times higher C amount, so 5 to 10 c a pre-pee test pill that causes 1000 different body chemicals to be visible at a 5 C gel bead 1mm active chemical pee test.
chronological interval of perfumed antibody delivery, ok, if you snort perfumed antibodies, they start circulating in 5-20 minutes, then possibly use another 20 minutes to glom onto some easy things at the circulation; If the perfumed antibodies perfume part is attached to a molecule that the kidney preferentially excretes, then it is possible that diagnostic, detectable amounts of perfume accumulate at the bladder in 15-30 minutes. So 45-50 minutes after you snort it, a pee test diagnostic reads what it says.

Comparing this to an oral perfumed antibody pill, an enteric coated pill, that fizzes automatically to dissolve at the part of the upper GI tract least destructive to antibodies; so it takes 4-6 hours before it fizzes and the perfumed antibodies can commence a 4 hour absorption to the circulatory system period. At 4.5 hours the bladder concentration of perfume from the perfumed antibodies is high enough to diagnose with a pee test. So an oral version is 8-10 hours after dosing to getting a diagnostic from the pee test.

Accumulation of perfume molecules at the bladder from attaching the perfume molecule to drugs that cause excretion of the chemical; (the perfume is after separating from the antibody that glommed a particular, protein, peptide, cytostructure, or chemical at the body, notably all the capillary containing tissues as well as all the material at the circulatory system.

So, a perfumed antibody could possibly travel through a capillary, sometimes make its way to the cytes adjacent to the capillaries epithilial lining, and sometimes actually attach to the chemically unique antibody glommable outer surface chemistry of an actual cancer cyte. Other times perfumed antibodies could just glom onto circulating biochemicals that are only produced at oncocytes, or possibly glom onto some protein or even leukocyte surface that goes with finding and glomming a systemic response to oncocytes and oncostructures. These all utilize antibodies to find cancer, or find cancer is basent.

perfumed antibodies that leukocytes and macrophages eat: noting that the perfumed antibodies that get eaten, then possibly digested at the vacuole of a leukocyte or macrophage: The perfumed antibody could be constructed and engineered to have molecular parts so durable they made it past vacuole digestion; the durable molecular parts being pooedout at the leukocytes or macrophages that leave durable molecular pieces that another different antibody is tuned to to cause a different perfumed antibody to glom it, and send sufficient perfume to the pee to say “leukocytes at the body are eating things that TGW300 glommed onto. TGW300 attaches to: highly easy to cure cancer cyte surface protein. So if the other perfumed antibody that glommed the biopolymer remains of the first immunochemical at the poo of the leukocyte or macrophage, is excreted at the bladder, then peeing on the test diganostic would say that leukocytes are meeting oncocytes at a person’s body.

Possibly strong popypeptides, or some other oligomer-like biopolymer like a custom-shaped starch (cyclodextrin or godel escher bach dextrin lumps that have high and unique antibody affinity), or the material degradable sutures are made from, or keratin.

perfumed antibodies at pee test during pregnancy describe fetal biochemistry from fetal metablic products that pass the placenta; paternity test while abortion pill still has weeks of available function and can abort if the pregnant person finds the genetics, personality, or situation of the paternal gene source to be nonoptimal from the pregnant person’s perspective.

technology I do not know: a drug, that is actively beneficial to a fetus and possibly also the mother, possibly a snortable peptide or protein, that, like antabuse prevents drinking EtOH. People could take this to benefit their fetus and potential baby, and as a side effect it would keep them from consuming EtOH, but I do not actually know how it works. some thing like antibodies to the actual eentsy molecule EtOH, that when they glom

perfumed antibody with fluorophores, three simultaneous antibody different chemical gloms, makes a 1 per thousand antibody glom false positive occurence go to a one per 100 million or 1 billion false positive occurrence if all three antibodies to completely different chemicals are there simultaneously.

That multi-antibody response to build a diagnosis is beneficial as a fluorophore antibody diagnostic could test 1000 different chemicals at fluid from the circulatory system; fluorophore:ATP:antibody a fluorophore with an ATP linking it to the chemical glomming antibody; when the antibody gloms, the ATP snaps off a PO4, and the fluorophore is then at the circulatory system, with part of an ATP such as an ADP or AMP attached to it, which makes it particularly distinguishable to the computer reading the fluid sample at the test (noting there would be fluorophores attached to unglommed antibodies, and that telling the difference between these and reacted fluorophores antibodies produces daignostic data at the test)
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All technologies, ideas, and inventions of Treon Sebastian Verdery are public domain at JUly 8,2023AD and previously, as well as after that date