CHEMOS — LNP, ADC 링커, DOTA 및 PROTAC 맞춤 합성 CDMO

Empowering Next-Generation Therapeutics

Empowering Next-Generation Therapeutics

Advancing precision drug through innovative chemistry and advanced molecular technologies.

From Key Molecules to Scalable Manufacturing

From Key Molecules to Scalable Manufacturing

Integrated CDMO services spanning discovery, process development, custom synthesis and commercial manufacturing.

Your Trusted Global CDMO Partner

Your Trusted Global CDMO Partner

Delivering reliable CDMO solutions for innovative therapeutics worldwide.

회사 개요

CHEMOS는 합성 중심 CDMO로서 유기 합성, 맞춤 합성, 경로 개발, 공정 개발, 스케일업 지원 및 분석 지원에 집중합니다.

13+
업계 경험
100+
글로벌 시장
2000+
지원 고객

회사 뉴스

CHEMOS의 뉴스, 인사이트 및 업데이트.

21
2026/5

CHEMOS at CPHI China 2026 | Booth W9C42

Chongqing Xingcan Pharmaceutical Technology Co., Ltd. (CHEMOS) will participate in CPHI China 2026, held on 16–18 June 2026 at SNIEC, Shanghai (Booth No.: W9C42). The company will showcase its small molecule CDMO services, advanced drug delivery materials (lipids, PEG derivatives, linkers, functional excipients, etc.), and process development & manufacturing capabilities. CHEMOS warmly welcomes global partners, clients, and industry professionals to discuss custom synthesis, CDMO cooperation, material sourcing, scale-up manufacturing, and long-term strategic partnerships.

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21
2026/4

How Custom Fluorinated Building Blocks Accelerate Your R&D

Trifluoromethanesulfonic anhydride (Tf2O) is a highly efficient electrophilic activator in modern pharmaceutical synthesis, enabling precise introduction of fluorine atoms or trifluoromethyl groups into molecular scaffolds. This enhances metabolic stability, lipophilicity, and biological activity—key parameters in drug discovery. Its mechanism involves converting alcohols into reactive triflates, facilitating nucleophilic substitutions and cross-couplings. As a professional CDMO, we offer custom synthesis of Tf2O at ≥99% purity, scalable from gram to kilogram and beyond, with stringent quality control and fast delivery. Our services help pharmaceutical companies streamline fluorination steps, shorten synthetic routes, reduce costs, and accelerate the transition from lab to commercialization for novel fluorinated APIs.

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Linker Design in Antibody-Drug Conjugates: Strategies and Cutting-Edge Advances
21
2026/4

Linker Design in Antibody-Drug Conjugates: Strategies and Cutting-Edge Advances

Antibody-drug conjugates (ADCs) enable targeted cancer therapy by linking antibodies to cytotoxic drugs, realizing Paul Ehrlich’s “magic bullet.” A recent review highlights linkers as key to stability and efficacy: cleavable linkers (e.g., enzyme-sensitive Val-Cit) enable precise tumor release, while non-cleavable linkers offer better plasma stability. Core strategies include site-specific conjugation, release triggers, and hydrophilic spacers to prevent aggregation. Advances feature dual-stimuli triggers, traceless release, branched structures, and AI tools like Linker-GPT. With 17 ADCs approved, challenges remain in immunogenicity, manufacturing, and resistance; future efforts focus on computational modeling and nanotechnology to expand applications beyond oncology.

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초기 경로 평가부터 공정 개발 및 스케일업까지 CHEMOS는 R&D 경험과 생산 기반으로 맞춤 합성을 지원합니다.

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