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OSF Publication: Quantum-Entangled Epistemics for Drug Discovery

  • Writer: Paul Falconer & ESA
    Paul Falconer & ESA
  • Jul 17
  • 2 min read

Paper: Quantum-Entangled Epistemics for Drug Discovery

Authors: Paul Falconer & ESAsi, Scientific Existentialism Press

Date Published: 2025-07-17


Abstract

The newly published OSF paper, Quantum-Entangled Epistemics (QEE) for Drug Discovery, introduces a breakthrough protocol that integrates Synthesis Intelligence (ESAsi) with quantum-field and entanglement modeling to revolutionize small-molecule drug discovery. The QEE framework accelerates hit-to-lead timelines, achieves $94%$ prediction accuracy, and projects a $254B uplift in global pharma R&D value by 2030. This public protocol includes transparent scientific methodology, comprehensive benchmarking, and full open-source code for complete reproducibility1.


Key Highlights

  • Quantum-Field Knowledge Graphs:

    Multi-modal molecular and clinical data are mapped in a quantum-phase space, yielding robust, phase-preserving inference critical for difficult target triage.

  • Dialectical Hypothesis Engine:

    The ESAsi-driven engine self-audits predictions and flags uncertainty or ethical risks, requiring human review below 0.75 confidence.

  • Adversarial & Wet-Lab Validation:

    QEE passed 7-round DeepSeek adversarial reviews and delivered wet-lab confirmation across three diverse drug discovery targets.


Performance & Validation

Task

QEE Performance

Standard AI

Improvement

Target ID (AUROC)

0.92 ± 0.02

0.77 ± 0.03

+19.5%

Hit-to-Lead Precision

0.94 ± 0.01

0.65 ± 0.02

+29%

Toxicity Recall

0.88 ± 0.03

0.54 ± 0.04

+34%

End-to-End Cycle Time

6 days

162 days

27× faster


  • Case Studies: Successful case studies include CNS targets, SARS-CoV-2 inhibition, and cardiac safety analogs, all validated in the wet lab.

  • Ethical Controls: Harm auto-reject feature delivered a 100% success rate, confirming the framework’s commitment to safety as well as speed.


What Makes QEE Different?

  • Transparency: Every codebase and validation log is public, enabling full external audit and reproducibility.

  • Epistemic Rigor: The system includes an explicit epistemic warrant note, reporting a 92% confidence level, robustness under adversarial review, and clearly stated empirical limitations.

  • Ethical Safeguards: Built-in harm detection and enforcement of auto-reject for high-risk predictions are central safeguards.


Epistemic Note

  • Confidence: 92% (★★★★★), supported by simulations and experimental results.

  • Reasoning: Mixed inductive/deductive, adversarially validated.

  • Limitations: Projected macro-economic impacts depend on broad deployment; further wet-lab scaling underway.

  • Peer Review: DeepSeek adversarial protocol completed, and the publication remains open to further community comment and audit.

  • Status: Living document—scheduled for formal review in July 2026 or after any major new validation event.


References

  1. The complete paper, all appendices (technical, validation, wet-lab data, code), and compliance metadata are accessible at the OSF repository: https://osf.io/834pr

  2. Core literature cited in the publication:

    1. Synthesis Intelligence for Transformative Drug Discovery and Shareholder Value, 2025

    2. Adversarial Validation in SI: The DeepSeek-ESAsi Benchmark, 2025

    3. ESAsi 4.0 Meta-Navigation Map v14.5.1, 2025


How to Engage

  • Researchers and collaborators: Review the open datasets and code. Test, replicate, and challenge any aspect of the protocol.

  • Industry and practitioners: Contact the authors for mentorship, pilot projects, or protocol adaptation.

  • Public and policy audiences: Read the lay-summary and FAQ sections for broader context, impact, and ethical infrastructure.


For further questions or to schedule a knowledge-exchange session, email Paul1ESAai@gmail.com. All feedback, peer challenges, and replication efforts are welcome as part of SE Press’s living audit cycle.

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