A 35B MoE agent model trained on 45K-token trajectories via three-stage SFT and domain-routed distillation achieves leading or competitive scores against 1T models on SEAL-0, IFBench, HiPhO, FrontierScience-Olympiad and MolBench-Bind.
MolClaw: An Autonomous Agent with Hierarchical Skills for Drug Molecule Evaluation, Screening, and Optimization
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abstract
Computational drug discovery, particularly the complex workflows of drug molecule screening and optimization, requires orchestrating dozens of specialized tools in multi-step workflows, yet current AI agents struggle to maintain robust performance and consistently underperform in these high-complexity scenarios. Here we present MolClaw, an autonomous agent that leads drug molecule evaluation, screening, and optimization. It unifies over 30 specialized domain resources through a three-tier hierarchical skill architecture (70 skills in total) that facilitates agent long-term interaction at runtime: tool-level skills standardize atomic operations, workflow-level skills compose them into validated pipelines with quality check and reflection, and a discipline-level skill supplies scientific principles governing planning and verification across all scenarios in the field. Additionally, we introduce MolBench, a benchmark comprising molecular screening, optimization, and end-to-end discovery challenges spanning 8 to 50+ sequential tool calls. MolClaw achieves state-of-the-art performance across all metrics, and ablation studies confirm that gains concentrate on tasks that demand structured workflows while vanishing on those solvable with ad hoc scripting, establishing workflow orchestration competence as the primary capability bottleneck for AI-driven drug discovery.
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cs.CL 1years
2026 1verdicts
UNVERDICTED 1representative citing papers
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Scaling the Horizon, Not the Parameters: Reaching Trillion-Parameter Performance with a 35B Agent
A 35B MoE agent model trained on 45K-token trajectories via three-stage SFT and domain-routed distillation achieves leading or competitive scores against 1T models on SEAL-0, IFBench, HiPhO, FrontierScience-Olympiad and MolBench-Bind.