Enyan Dai


2026

Goal-directed molecular generation requires satisfying heterogeneous constraints such as protein–ligand compatibility and multi-objective drug-like properties, yet existing methods often optimize these constraints in isolation, failing to reconcile conflicting objectives (e.g., affinity vs. safety), and struggle to navigate the non-differentiable chemical space without compromising structural validity. To address these challenges, we propose CAGenMol, a condition-aware discrete diffusion framework over molecular sequences that formulates molecular design as conditional denoising guided by heterogeneous structural and property signals. By coupling discrete diffusion with reinforcement learning, the model aligns the generation trajectory with non-differentiable objectives while preserving chemical validity and diversity. The non-autoregressive nature of diffusion language model further enables iterative refinement of molecular fragments at inference time. Experiments on structure-conditioned, property-conditioned, and dual-conditioned benchmarks demonstrate consistent improvements over state-of-the-art methods in binding affinity, drug-likeness, and success rate, highlighting the effectiveness of our framework. The code is available at https://github.com/Lee612-1/CAGenMol.
Large language models (LLMs) are considered valuable Intellectual Properties (IP) due to the enormous computational cost of training, making their protection against malicious stealing or unauthorized deployment crucial.Despite efforts in watermarking and fingerprinting, existing methods either affect text generation or rely on white-box access, limiting practicality.To address this, we propose DuFFin, a novel Dual-Level Fingerprinting framework for black-box ownership verification.DuFFin jointly extracts trigger patterns and knowledge-level fingerprints to identify the source of a suspect model.We conduct experiments on diverse open-source models, including four popular base LLMs and their fine-tuned, quantized, and safety-aligned variants released by large companies, start-ups, and individuals.Results show that DuFFin accurately verifies the copyright of protected LLMs on their variants, achieving an IP-ROC greater than 0.99.Our code is available at https://github.com/yuliangyan0807/llm-fingerprint.
Cost-aware routing dynamically dispatches user queries to models of varying capability to balance performance and inference cost. However, the routing strategy introduces new security concern that adversaries may manipulate router to consistently select expensive high-capability models. Existing routing attacks depend either on white-box access or heuristic prompts, rendering them ineffective in real-world black-box scenarios. In this work, we propose R2A, which aims to mislead black-box LLM routers to expensive models via adversarial suffix optimization. Specifically, R2A deploys a hybrid ensemble surrogate router to mimic the black-box router. A suffix optimization algorithm is further adapted for the ensemble-based surrogate. Extensive experiments on multiple open-source and commercial routing systems demonstrate that R2A significantly increases the routing rate to expensive models on queries of different distributions. Code and examples: https://github.com/thcxiker/R2A-Attack.

2020

The competition of extracting COVID-19 events from Twitter is to develop systems that can automatically extract related events from tweets. The built system should identify different pre-defined slots for each event, in order to answer important questions (e.g., Who is tested positive? What is the age of the person? Where is he/she?). To tackle these challenges, we propose the Joint Event Multi-task Learning (JOELIN) model. Through a unified global learning framework, we make use of all the training data across different events to learn and fine-tune the language model. Moreover, we implement a type-aware post-processing procedure using named entity recognition (NER) to further filter the predictions. JOELIN outperforms the BERT baseline by 17.2% in micro F1.