INNOVATION FIRST · SCIENCE POWERED · AI ACCELERATED 源头创新 · 科学驱动 · AI加速

Reshaping drug discovery with AI large models and atomic-level structural biology AI生物大模型 与冷冻电镜结构生物学 重构新药发现范式

GenTide Biotech is an international innovative drug enterprise powered by an AI Bio-Large Model Platform. We integrate AI with Cryo-EM structural biology to discover first-in-class therapies in metabolic disease, pain, oncology, and aging. 睿联生物科技是一家以AI生物大模型平台为核心发动机的国际化创新药企业。 我们深度融合人工智能与冷冻电镜结构生物学,在代谢疾病、疼痛管理、 肿瘤治疗与抗衰老领域开发 first-in-class 创新药。

Explore the Platform 了解技术平台 View Pipeline 查看研发管线
Platform Performance 平台性能

Faster, cheaper, higher hit rate 更快、更低成本、更高命中率

Our AI-driven DTBL closed-loop compresses drug discovery timelines while improving the chances of delivering a viable clinical candidate. 我们的 AI 驱动的 DTBL 研发闭环大幅缩短新药发现周期, 同时显著提升临床前候选化合物的命中率与成药性。

40%↓
R&D Time Reduction 研发周期缩短
70%↓
Cost Savings 成本降低
50%↑
Hit Rate Increase 命中率提升
20–50×
Targeting Enhancement 靶向浓度提升
Science First 科学是根基

AI is only as good as the science underneath it. We never forget that. AI 的上限,取决于它所依托的科学根基。 我们从不忘记这一点。

GenTide's edge is not a software stack — it is the combination of deep biological insight and AI that makes each other sharper. Our algorithms are built on published research. Our models are trained on real structural data. Our hypotheses are tested in actual cells and in-vivo. 睿联的竞争力不是一套软件栈——而是深度生物学洞察与 AI 的结合,二者互相磨砺、相互增益。 我们的算法建立在已发表的研究之上。我们的模型用真实结构数据训练。 我们的假设在真实细胞和体内模型中验证。

Algorithms grounded in biology 算法根植于生物学

NBI, SGEDiff, ComplexDnet — models developed from first-principles structural biology research, not fine-tuned generalist LLMs. NBI、SGEDiff、ComplexDnet——从第一性原理结构生物学研究中发展而来的模型,而非通用 LLM 微调。

Cryo-EM closes the loop 冷冻电镜形成闭环

Atomic-resolution structural validation in-house — not outsourced. Each structure solved feeds directly back into the next generation of AI models. 原子分辨率结构验证在内部完成,不外包。每一张解析的结构直接反馈到下一代 AI 模型。

Technology serves the pipeline 技术服务于管线

Every platform investment is justified by its ability to produce better drug candidates faster. We build what we need to win. 每项平台投资都以能否更快产出更好的候选药物为衡量标准。我们只构建赢所必需的能力。

Why GenTide 为什么选择睿联

Four core differentiators 四大核心差异化优势

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AI-First Algorithmic Base AI First 算法基座

10+ core algorithms and a 10M+ compound library drive source-innovation and a high-druggability chemical space. 10+ 核心算法与千万级分子库,驱动源头创新, 构建高成药性化学空间。

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Original Anti-Aging Target 原创抗衰靶点突破

Novel PAGln/PAA pro-aging mechanism backed by Nature Aging publications and proprietary p16 reporter mice. 揭示全新 PAGln/PAA 促衰老致病机制, 发表于 Nature Aging,依托独家 p16 报告基因小鼠。

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DTBL Efficient R&D Loop DTBL 高效研发闭环

Seamless dry-wet experiment synergy solves the high trial-and-error cost of traditional drug discovery. 干湿实验无缝协同,破局传统新药发现试错成本极高的行业痛点。

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Global Synergistic Network 全球化协同网络

US / Singapore / China global layout with full NMPA + FDA dual IND filing capability. 美国 / 新加坡 / 中国全球布局, 具备 NMPA 与 FDA 中美双报核心能力。

Strategic R&D Directions 四大战略研发方向

Four programs targeting large unmet needs 聚焦四大未满足医疗需求

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Multi-target Peptides 多靶点多肽

GLP-1R / GIPR / GCGR tri-agonist for metabolic disease and obesity. GLP-1R / GIPR / GCGR 三靶点激动剂,靶向代谢疾病与肥胖。

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Non-opioid Analgesics 非阿片镇痛剂

Nav1.8 selective inhibitor — safer pain management without addiction risk. Nav1.8 选择性抑制剂,消除成瘾风险的安全镇痛方案。

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Multi-target TKI 多靶点 TKI

MET / RET / ROS1 allosteric inhibitor with AI conjugates to overcome resistance. 针对 MET / RET / ROS1 的变构抑制剂,AI 偶联突破耐药。

Anti-Aging Drugs 抗衰新药

β2-AR original mechanism with PAGln/PAA validation loop. β2-AR 原创机制,PAGln/PAA 促衰老验证闭环。

Business Model 商业模式

Three revenue tracks, de-risked by design 三条收入来源,内置风险分散

GenTide runs a dual-track model — pipeline assets plus platform services — so early-stage milestones generate real cash flow while the major programs advance. GenTide 采用"管线资产 + 平台服务"双轨模式,让早期里程碑即产生真实现金流, 同时推动核心管线持续前进。

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Platform Enablement 平台服务收入

Open the DTBL + Cryo-EM platform to pharma partners under a fee-plus-milestone model. Stable early cash flow while validating platform value and building License-out relationships. 向大型药企开放 DTBL + 冷冻电镜平台,收取服务费 + 里程碑费用。 早期最稳定的现金流来源,同时验证平台价值,为后续授权铺路。

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Asset-Level Licensing 管线资产授权

At PCC or IND stage, license regional rights to big pharma for upfront + milestone + royalties. Nav1.8 is the leading License-out candidate targeting US/EU rights. Target: ¥80M–120M near-term, ¥500M–800M mid-term. 在 PCC 或 IND 节点将地区权益授权给大药企,收取预付款 + 里程碑 + 销售分成。 Nav1.8 为首要 License-out 候选。近期目标 8,000 万—1.2 亿元,中期 5—8 亿元。

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Regional Co-Development 区域联合开发

Retain Greater China rights, partner with US/Europe for co-funded clinical development. Shared risk, shared upside — without diluting our core China market position. 保留大中华区权益,与美国 / 欧洲合作伙伴联合资助临床开发。 风险共担、收益共享,同时保留中国市场核心地位。

Milestones 战略里程碑

2026 — 2030 roadmap 2026 — 2030 研发路线图

2026
Q2–Q3Q2–Q3

Platform Validation平台验证期

Core team assembled · DTBL data pipeline live · GLP-1 & Nav1.8 in-vitro positive data核心团队到位 · DTBL 数据管道上线 · GLP-1 & Nav1.8 体外阳性数据

2026
Q3–Q4Q3–Q4

First PCC Candidates首批 PCC 候选确认

GLP-1 PCC confirmed · Nav1.8 in-vivo validation · β2-AR PCC announced · DTBL first full closed-loopGLP-1 PCC 确认 · Nav1.8 体内验证阳性 · β2-AR PCC 宣布 · DTBL 首次完整闭环

2027

IND-Enabling StudiesIND 使能研究

GLP-1 & Nav1.8 IND-enabling studies launched · First CMC filing drafted · TKI PCC confirmedGLP-1 & Nav1.8 IND 使能研究启动 · 首份 CMC 文件起草 · TKI PCC 确认

2028 ⭐

Dual IND Approval中美双 IND 获批

Nav1.8 + GLP-1 IND approved (NMPA & FDA dual-track) · Nav1.8 first License-out LOI signedNav1.8 + GLP-1 双 IND 获批(中美双轨)· Nav1.8 首个 License-out LOI 签署

2028–29

First Patients首例患者入组

Nav1.8 Phase I enrollment begins · GLP-1 Phase I starts · Major License-out deal closedNav1.8 I 期首例入组 · GLP-1 I 期启动 · 首个重大 License-out 完成

2030+

Clinical Data Readout临床数据读出

Nav1.8 Phase I/II data · GLP-1 Phase II designed · β2-AR clinical path definedNav1.8 I/II 期数据读出 · GLP-1 II 期方案设计 · β2-AR 临床路径明确