We pioneer integrated cyclic peptides target R&D via AI prediction and experimental validation.
Based on multi-omics data and self-developed AI models, we screen cyclic peptides-suitable targets from disease pathways, focusing on undruggable PPI, GPCR and IDPs. We conduct druggability evaluation, binding analysis and functional verification at cellular and animal levels.
We have built a professional evaluation system for cyclic peptides targets, effectively lowering early R&D risks and boosting the success rate of cyclic peptides drug development.
Based on Sungening Bio’s internationally leading mRNA display technology derived from the PURE system, we construct cyclic peptides libraries with a scale of up to 10¹³. Catering to the screening demands for specific targets (such as protein-protein interaction interfaces and proteins without active pockets), we deliver high-affinity cyclic peptides hit sequences within weeks.
We support high-throughput screening of cyclic peptides hit molecules against undruggable targets, enabling the de novo discovery of cyclic peptides ligands for complex protein-protein interaction interfaces.
Conduct in-depth chemical modification and affinity enhancement of cyclic peptides hit molecules. Systematically introduce tens of thousands of druggable building blocks such as unnatural amino acids and heterocyclic structures into the hit scaffold to construct a cyclic peptides-building block conjugate library. Through high-throughput affinity screening, rapidly identify super binders with elevated affinity and improved druggability after unnatural modification.
We leverage integrated physical models and AI for computation-driven drug design.
We offer full computational support from target analysis, binding pocket recognition to virtual screening and molecular optimization.
We generate novel cyclic peptides via deep learning, apply FEP and molecular dynamics to assess binding affinity, and conduct early ADMET prediction to lower wet-lab costs.
We break the druggability bottleneck of innovative drugs from lead compounds to clinical candidates via systematic in vitro ADMET screening, early toxicity assessment, pre-formulation and in vivo PK/PD studies.
We advance druggability evaluation alongside efficacy optimization, and build structure-property databases to deliver full solutions for high-quality PCC development.
Sungening has optimized multiple projects such as SG6001 and SG1001 with solid practical experience.
We offer full-cycle localized commercialization services for cyclic peptide drug R&D assets throughout their entire lifecycle.
We cover patent planning & risk assessment, value appraisal, clinical and market-based valuation reports, as well as partnership matchmaking and licensing including technology transfer, joint development and exclusive authorization. We also provide financing support and pipeline incubation to maximize commercial value and accelerate industrialization.