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High-purity Insulin Degludec Side Chain, Semaglutide, Tirzepatide, and Liraglutide intermediates. Trusted by global pharmaceutical innovators for R&D and GMP production.
Pukang specializes in high-purity intermediates and functional building blocks for peptide therapeutics, ADCs, PROTACs, RNAi, and advanced drug delivery systems.
High-purity side chain and modified amino acids for GLP-1 analog synthesis. Used in diabetes and obesity therapeutics.
Specialized side chain for ultra-long-acting insulin analogs. Critical for basal insulin formulations.
Dual GIP/GLP-1 receptor agonist building blocks. Includes fatty acid spacers and modified residues.
C16 fatty acid-modified glutamic acid derivatives for GLP-1 analogs. Used in weight management and diabetes.
Functionalized PEGs for bioconjugation, solubility enhancement, and half-life extension in biologics.
Precision linkers for ADC, PDC, PROTAC, and RDC platforms. Cleavable and non-cleavable options.
SNAC, Baricitinib, Eptifibatide, and dipeptides for oral peptide delivery and small molecule APIs.
Comprehensive molecular block library for next-gen long-acting peptide drugs. Rapid screening and customization.
Chengdu Pukang Biotechnology Co., Ltd. was founded in 2008 and is located in the National Cross-Strait Science and Technology Industry Development Park, Chengdu. We specialize in the R&D, production, and global supply of polypeptide modifiers, advanced excipients, and specialty intermediates.
As an integrated manufacturer, Pukang operates a 2,400 sqm R&D center and a 1,000 sqm GMP-compliant production workshop. Our team brings deep expertise in organic synthesis, peptide chemistry, and process scale-up to deliver high-quality products for pharmaceutical innovation.
Pukang combines cutting-edge organic synthesis with scalable manufacturing to deliver reliable, high-purity intermediates for life-saving therapies.
From mg to kg scale, we support custom routes, route scouting, and optimization for complex molecules.
We bridge lab-scale synthesis to pilot and commercial production with robust, reproducible processes.
Strict QC protocols with HPLC, LC-MS, NMR, and elemental analysis ensure batch-to-batch consistency.
Documentation, CoA, and regulatory files available for IND, NDA, and DMF submissions.
Proprietary side chains and molecular blocks for next-generation long-acting peptide drugs.
Trusted partner for biotech and pharma companies across North America, Europe, and Asia.
Tailored synthesis of novel intermediates, side chains, and building blocks based on client specifications.
Route scouting, optimization, and impurity profiling for cost-effective and scalable manufacturing.
Full characterization using HPLC, LC-MS, NMR, and elemental analysis. Method development available.
From gram to multi-kilogram scale with strict process control and documentation.
CoA, stability data, and regulatory files for IND, NDA, and DMF submissions.
Technical consultation and freedom-to-operate analysis for novel peptide therapeutics.
Contact our team for product inquiries, custom synthesis, or technical support.
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