CHEMOS — CDMO de síntesis a medida para LNP, enlazadores ADC, DOTA y PROTAC

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.

Perfil de la empresa

CHEMOS es un CDMO impulsado por la síntesis, centrado en síntesis orgánica, síntesis a medida, desarrollo de rutas, desarrollo de procesos, apoyo al escalado y soporte analítico. Trabajamos con materiales de administración avanzada de fármacos, bloques de bioconjugación, quelantes radiofarmacéuticos, intermediarios PROTAC y compuestos orgánicos especializados.

13+
Años de experiencia
100+
Mercados globales
2000+
Clientes atendidos

Noticias de la empresa

Noticias, perspectivas y actualizaciones de CHEMOS.

17
2026/7

Lipfendra Approval Puts Oral Macrocyclic Peptide Process Design in Focus

FDA announced on July 16, 2026 that Lipfendra (enlicitide) was approved to be used with diet and exercise to reduce LDL-C in adults with high cholesterol or heterozygous familial hypercholesterolemia. FDA also states that Lipfendra is a tablet taken by mouth once daily and is the first oral therapy that blocks PCSK9.

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17
2026/7

LUNA18 Shows Why N-Alkyl-Rich Cyclic Peptides Need Route-Specific Process Design

The key correction is that the ACS Organic Process Research & Development paper describes LUNA18 (paluratide) through a liquid-phase peptide synthesis process, not a simple SPPS plus three-fragment route. The paper’s abstract says the authors departed from conventional solid-phase peptide synthesis and developed an LPPS process for an N-alkyl-rich cyclic undecapeptide KRAS inhibitor.

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Reported Inclisiran GalNAc-siRNA Architecture: Conjugation and DMPK
17
2026/7

Reported Inclisiran GalNAc-siRNA Architecture: Conjugation and DMPK

The reported inclisiran architecture illustrates why an siRNA conjugate cannot be reduced to a sequence plus a targeting ligand. Descriptions of that architecture place a triantennary N-acetylgalactosamine (GalNAc) unit at the sense-strand terminus, combine 2'-fluoro and 2'-O-methyl ribose substitutions with terminal phosphorothioate linkages, and rely on the antisense strand for RNA-induced silencing complex (RISC) loading. Each element addresses a different constraint: cell uptake, nuclease exposure, strand handling, or intracellular recognition.

Contacto

Conecte su proyecto con un equipo químico práctico

Desde la evaluación temprana de una ruta hasta el desarrollo de procesos y el escalado, CHEMOS ofrece soporte de síntesis a medida basado en experiencia de I+D y base productiva.

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