NIASCEND | Dr. Dmitry Kats (@NIASCEND) header
NIASCEND | Dr. Dmitry Kats (@NIASCEND) profile picture

Epid @UNCpublichealth | Biostats @usfcoph | Math/CS @XavierU | Biochem @TulaneCBE || 🚀 Ascending beyond just healthy aging mandates https://teapawt.net/t.co/JE2bhVjCml 💎

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Joined October 2023
Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)Photo by NIASCEND | Dr. Dmitry Kats (@NIASCEND)
Imagine when AI consistently generates—not some estimate—but the EXACT causal effect of ANY intervention on ANY outcome possible—down to the VERY DAY it happens! By 2020, I already did. We—@OpenAI, @Merck, & I—seek fellow frontierists ready to lead… 🎯 aging-us.com/article/102916/…
🤖 Made with AI
NA proves it’s the ONLY NAD choice BY the flush—not balk but SIGN of enough potential energy flux as NAADP through NAD/NADP for excess energy expenditure vs accrual along aging/disease that’s STRONGER than exercise—shaking potential energy out stores—exposing NAM/NMN/NR as futile
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NIASCEND | Dr. Dmitry Kats retweeted
Replying to @AlanaDLevin
Wonder why…
Early-life antibiotic dysbiosis impairs microbial tryptophan-nicotinic acid metabolism exacerbating food allergy in adulthood sciencedirect.com/science/ar…
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NIASCEND | Dr. Dmitry Kats retweeted
That they don’t even realize what tryptophan is for?
Early-life antibiotic dysbiosis impairs microbial tryptophan-nicotinic acid metabolism exacerbating food allergy in adulthood sciencedirect.com/science/ar…
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NIASCEND | Dr. Dmitry Kats retweeted
Replying to @AlanaDLevin
But not this eh?
Early-life antibiotic dysbiosis impairs microbial tryptophan-nicotinic acid metabolism exacerbating food allergy in adulthood sciencedirect.com/science/ar…
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They got these people fiendin
bms is literally one of the six partners, big pharma already said yes
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This is money laundering.
Surprise 1: Anthropic acquired a one-person biotech . . . Surprise 2: that person is me Surprise 3: I’m here to tell you all about it Yes, this is what you think it is; after 6 yrs of increasingly loose anonymity: the Professor Oak reveal post …and yes, it has gotten so boring around here that I’m literally doxxing myself to spice up the timeline ------- Ok, allow me to introduce myself. My name is Cody Tranbarger. I mostly tweet, but occasionally find time to dabble in drug dev & starting/building biotechs. My past lives span the VC, crossover, startup continuum; Prof Oak has been my way of keeping a digital foot in those worlds, despite having my physical feet planted elsewhere. The past 18 mo, ‘elsewhere’ was Mithril Medicine, a co. I founded to develop bsAbs for LAMA2-CMD & other ECM-related genetic diseases. Mithril was born out of hands-on building with @MikeNGladstone, @JasonPaulRhodes, @LifeSciVC, & team @atlasventure. Somehow, I made enough half-decent calls along the way (even a broken clock is right twice a day, eh?) to convince them Mithril/I warranted a small seed. While I can hardly rationalize such an outrageously cavalier bet, I’m grateful for it, & I'd partner with Atlas again in a heartbeat. In typical AV fashion, Mithril’s primordial form was virtual, decentralized, & ultra-lean. This stage tends to be short-lived, but for Mithril, it worked surprisingly well, for surprisingly long, thanks in part to the rapid maturation of the AI tools I used liberally. Eventually, Mithril became a bit of an experiment itself - to find the upper bound of how far it could scale as a single operator + a bunch of Claude (+ a stellar bench of part-time consultants). In parallel, I started spending time with @nc_frey, @an1lam, & @CoefficientBio team; and promptly experienced, for the 1st time, AI at the frontier. Soon thereafter, Mithril stopped looking like an experiment, & started looking like a preview of an entirely new operating model. From that spark came “Pipeline-in-a-Person.” The idea immediately resonated when we shared it here back in April; and it was central to the shared vision that led to Anthropic’s acquisition of Mithril, & my joining the team. Why join Anthropic? Three reasons. (1) For Mithril, the programs continue, with more resources & infrastructure behind them, and as much Claude as I can put to work. (2) For me, the chance to start several more programs, & find out how many one person can actually run in parallel - an almost unprecedented luxury for a curious drug hunter. (3) For our mission, a path to institutionalize & scale this new way of working, then put it in the hands of all of biopharma, all over the world - which, candidly, I find the most energizing. Will AI x Bio cure diseases? Unequivocally yes, imo… but not by the route that gets the most airtime. Rather than timeline acceleration & compression, I see orchestration & parallelization as today's low-hanging fruit. Most drug hunters see a handful of go/no-go calls in a career, & spend entirely too much of the rest trading emails (my inbox can attest). Give them the bandwidth to run several programs at once, and the time to focus on scientific judgment, and I’m willing to bet they’ll make better calls. And at scale, better calls translate to more drugs, higher hit rates, broader patient impact, & likely, a disease or 10 or 100 cured. I couldn't be more excited to build toward that future @AnthropicAI. Finally, a heartfelt thank you to BioTwitter/X. The end of anonymity is bittersweet, but if anyone’s earned a proper introduction, you all have. It’s difficult to overstate how much this app has done for me: a decade of education, plenty of friends, many job opportunities, several mentors, a few investors, even a co-founder (fmr). It was the generosity of this community that inspired me to start posting 6 years ago, after just as many years lurking. I hope I’ve been able to pay it forward, in my own small way. But, to be clear, Prof Oak isn’t going anywhere. Same beat, same themes, and now, a front-row seat to drug development at the frontier. Stay tuned for dispatches from the trenches; and remember... Gotta Cure 'Em All
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Hire an avatar and pay "them" absurdly
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7/9 COVID accelerates inflammatory Trp degradation, draining the Trp pool needed to maintain and regenerate tissue. Nicotinic acid specifically activates HCAR2/GPR109A—but niacin alone cannot rebuild Trp-dependent tissue or receptor protein once that substrate has been depleted.
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Catch up!
Mainstream longevity marketing reframed the harmless flush as a structural flaw to push patented, non-flushing amides like NMN & NR, steering public focus away from direct nicotinic acid, locking consumers into fruitless derivative pathways, and hiding the kinetic reality. (1/6)
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NIASCEND | Dr. Dmitry Kats retweeted
Imagine when AI consistently generates—not some estimate—but the EXACT causal effect of ANY intervention on ANY outcome possible—down to the VERY DAY it happens! By 2020, I already did. We—@OpenAI, @Merck, & I—seek fellow frontierists ready to lead… 🎯 aging-us.com/article/102916/…
🤖 Made with AI
NA proves it’s the ONLY NAD choice BY the flush—not balk but SIGN of enough potential energy flux as NAADP through NAD/NADP for excess energy expenditure vs accrual along aging/disease that’s STRONGER than exercise—shaking potential energy out stores—exposing NAM/NMN/NR as futile
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NIASCEND | Dr. Dmitry Kats retweeted
NA proves it’s the ONLY NAD choice BY the flush—not balk but SIGN of enough potential energy flux as NAADP through NAD/NADP for excess energy expenditure vs accrual along aging/disease that’s STRONGER than exercise—shaking potential energy out stores—exposing NAM/NMN/NR as futile
The [anti-inflammatory] flush [which for those more pellagric from the start is far less hostile coming w/ necessary tryptophans to restore tissue niacin binds to—GPR109A—that grew fried away as a result of decades w/o niacin]—remember—is nothing more than a random “side effect”!
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Quite a haunted house 🏚️
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NIASCEND | Dr. Dmitry Kats retweeted
I would take HOM3OSTASIS.com/NIASCEND seriously—and monogamously Tryptophan-Nicotinic Acid Metabolism in Patients with Tumours of the Bladder and Kidney pmc.ncbi.nlm.nih.gov/article… Cheers!
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NIASCEND | Dr. Dmitry Kats retweeted
Not cures. But many treatments can get you back to a functional human. Have you tried Niacin therapy? Helped me bigtime in 2020 then they wiped @NIASCEND off the social medias
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NIASCEND | Dr. Dmitry Kats retweeted
Marketing amides over nicotinic acid defies logic. NMN, NR, and NAM start behind, choked by deamidation bottlenecks that can never yield or realize high-level NA flux. Paying a premium for amides buys an inherently throttled pathway that fails where direct NA succeeds.
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NIASCEND | Dr. Dmitry Kats retweeted
Mainstream longevity marketing reframed the harmless flush as a structural flaw to push patented, non-flushing amides like NMN & NR, steering public focus away from direct nicotinic acid, locking consumers into fruitless derivative pathways, and hiding the kinetic reality. (1/6)
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NIASCEND | Dr. Dmitry Kats retweeted
Commercial amides hit strict low-capacity NAMPT limits, requiring slow, rate-limited deamidation just to yield free nicotinic acid, meaning they deliver only a weak, metered trickle instead of the uncompromised metabolic surge required for real disease reversal. (2/6)
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NIASCEND | Dr. Dmitry Kats retweeted
While conventional studies track static, superficial biomarker snapshots, my advanced MCMC-simulated Bayesian joint models of life-course ARIC cohort data—rigorously accounting for non-ignorable attrition—proved uncompromised nicotinic acid flux is completely irreplaceable. (3/6)
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NIASCEND | Dr. Dmitry Kats retweeted
Chronic cellular stress creates an unrelenting metabolic demand for NAD+, rapidly draining and degrading natural tryptophan reserves through inflammatory cascades, leaving cellular engines completely underpowered when patched with dead-end amides. (4/6)
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