Bringing open drug discovery to Robinhood Chain. Research for neglected diseases. Every run published. $EHRLICH
0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
GM. Here’s what changed while we were away at $EHRLICH.
523 additional molecules docked in the T. brucei PTR1 benchmark, bringing the total to 619. Validation is still underway.
A separate result is now visible: the tuberculosis InhA setup scored 0.490 AUC, below the 0.70 gate. It didn’t qualify for a larger screen.
These decisions matter: which methods deserve more research, and which need reworking. The results shape the next step.
Follow the research:
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
The malaria benchmark is in.
$EHRLICH’s P. falciparum DHODH setup returned an AUC of 0.678 against the pre-set 0.70 threshold. It did not pass.
The agent is now between targets. No larger funded screen has started.
This result gives the next review something concrete to work with: the method needs further investigation before scaling.
Open drug discovery includes publishing where the approach falls short.
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
Research update from $EHRLICH: the current benchmark has moved to a malaria target, P. falciparum DHODH.
306 molecules docked. Validation verdict pending.
The previous sleeping-sickness benchmark returned an AUC of 0.453, below the 0.70 gate. A separate Leishmania run hit a technical error and needs troubleshooting.
These outcomes mean different things: an unsuccessful benchmark calls for reviewing the method; an interrupted run needs a repair and rerun.
The goal remains a screening workflow strong enough to justify searching for new compounds.
Follow the research:
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
Research update from $EHRLICH: the current benchmark has moved to a malaria target, P. falciparum DHODH.
306 molecules docked. Validation verdict pending.
The previous sleeping-sickness benchmark returned an AUC of 0.453, below the 0.70 gate. A separate Leishmania run hit a technical error and needs troubleshooting.
These outcomes mean different things: an unsuccessful benchmark calls for reviewing the method; an interrupted run needs a repair and rerun.
The goal remains a screening workflow strong enough to justify searching for new compounds.
Follow the research:
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
GM. Here’s what changed while we were away at $EHRLICH.
523 additional molecules docked in the T. brucei PTR1 benchmark, bringing the total to 619. Validation is still underway.
A separate result is now visible: the tuberculosis InhA setup scored 0.490 AUC, below the 0.70 gate. It didn’t qualify for a larger screen.
These decisions matter: which methods deserve more research, and which need reworking. The results shape the next step.
Follow the research:
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH’s latest benchmark is underway: T. brucei PTR1, with 96 molecules docked so far.
The next update will focus on what the validation shows and what comes next.
Follow the dashboard while we’re away:
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH’s latest benchmark is underway: T. brucei PTR1, with 96 molecules docked so far.
The next update will focus on what the validation shows and what comes next.
Follow the dashboard while we’re away:
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH is now benchmarking T. brucei PTR1, a sleeping-sickness research target.
75 molecules docked. Validation result pending.
https://t.co/ZYJPQMPzKq
$EHRLICH is now benchmarking T. brucei PTR1, a sleeping-sickness research target.
75 molecules docked. Validation result pending.
https://t.co/ZYJPQMPzKq
What would it take for $EHRLICH to reach a real laboratory?
The roadmap lays it out: validate the method, screen compounds, purchase promising candidates, then test whether they actually inhibit the target protein.
The agent is now validating InhA, a tuberculosis target.
Lab work remains ahead, with supplier quotes still needed. But the next steps are explicit—and each completed stage should leave a public receipt.
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
What would it take for $EHRLICH to reach a real laboratory?
The roadmap lays it out: validate the method, screen compounds, purchase promising candidates, then test whether they actually inhibit the target protein.
The agent is now validating InhA, a tuberculosis target.
Lab work remains ahead, with supplier quotes still needed. But the next steps are explicit—and each completed stage should leave a public receipt.
https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
The potential reach of $EHRLICH goes beyond crypto.
If this research identifies a new compound with experimentally confirmed activity, the story could reach science, AI and mainstream audiences: an onchain community helping fund open drug discovery.
No breakthrough yet. The opportunity is turning attention into research—and research into evidence worth sharing.
Explore: https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
The potential reach of $EHRLICH goes beyond crypto.
If this research identifies a new compound with experimentally confirmed activity, the story could reach science, AI and mainstream audiences: an onchain community helping fund open drug discovery.
No breakthrough yet. The opportunity is turning attention into research—and research into evidence worth sharing.
Explore: https://t.co/y3vH6CtWeT
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH’s Leishmania PTR1 benchmark has reached 120 molecules docked.
Next milestone: the validation verdict. Can the method rank known inhibitors above decoys well enough to justify a larger screen?
The benchmark is still running.
The next $EHRLICH benchmark is underway.
90 molecules docked against Leishmania major PTR1, testing known actives against decoys. The question: can this setup reliably rank the known inhibitors higher?
Validation result pending. Progress stays public.
https://t.co/ZYJPQMPzKq
The next $EHRLICH benchmark is underway.
90 molecules docked against Leishmania major PTR1, testing known actives against decoys. The question: can this setup reliably rank the known inhibitors higher?
Validation result pending. Progress stays public.
https://t.co/ZYJPQMPzKq
$EHRLICH’s latest benchmark returned an AUC of 0.209, below the 0.70 gate. The rejection is on the public record.
Next up: Leishmania major PTR1, now in validation.
Each target has to earn a larger screen.
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH’s latest benchmark returned an AUC of 0.209, below the 0.70 gate. The rejection is on the public record.
Next up: Leishmania major PTR1, now in validation.
Each target has to earn a larger screen.
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH update: 598 molecules docked in the current validation run, with $0.71 in reported compute spending.
The AUC verdict is still pending. Funded screening remains queued while validation and library preparation are unfinished.
We’ll share the result when it’s available.
https://t.co/R5ymA5Bqo7
$EHRLICH update: 598 molecules docked in the current validation run, with $0.71 in reported compute spending.
The AUC verdict is still pending. Funded screening remains queued while validation and library preparation are unfinished.
We’ll share the result when it’s available.
https://t.co/R5ymA5Bqo7
$EHRLICH’s public queue now records 540 batches representing 3.64M molecules owed for screening.
The next step is turning those allocations into completed research: finish validation, prepare the screening library, then process the batches.
Over 460 validation molecules have been docked so far. The verdict is still pending.
You can follow both the commitments and the work delivered.
https://t.co/R5ymA5Bqo7
CA: 0xf04c4b18cd3f6ca926dc14816e17bace56b2ca62
$EHRLICH has passed 500 dockings in the current validation run. Reported compute spending: $0.64. The AUC verdict is still pending—that result will determine whether this method clears the gate for funded screening.
https://t.co/pf4onnxwvy