AICAR (5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside, CAS 2627-69-2) is a nucleoside analog widely used in metabolic and cardiovascular research as a direct AMPK activator. Reference standard for AMP-activated protein kinase pathway studies, exercise-mimetic mechanism research, and preclinical cardioprotection assays. ≥98% HPLC purity, MS-verified identity, per-lot CoA. Not for human or veterinary use.
We maintain regulatory dossiers in the following jurisdictions for AICAR (Acadesine)-relevant molecules. Letter of Authorization (LoA) and CEP / DMF / ASMF references are issued at no charge to qualified buyers.
AICAR (Acadesine) is supplied as a pharmaceutical-grade peptides for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using AICAR (Acadesine) typically reference it under CAS Registry Number 2627-69-2.
Our AICAR (Acadesine) is manufactured under WHO-GMP and ISO 9001:2015 conditions in Pune, India. Per-batch Certificate of Analysis (CoA) is released against USP / Ph. Eur. / IP / JP specifications depending on destination market. We hold US FDA Drug Master File and EDQM Certificate of Suitability dossiers for the molecules where regulatory recognition is required; Letter of Authorization (LoA) is issued at no charge to qualified buyers.
Quote requests for AICAR (Acadesine) are turned around within 24 business hours (IST, Pune). Bulk APIs typically ship within 7-10 business days of confirmed PO; air freight to North America and Europe runs 4-5 days door-to-door. Sample agreements are signed before shipping QC-grade material to your formulation laboratory.
We export AICAR (Acadesine) to 50+ countries including the United States, Canada, Mexico, Brazil, the European Union, the United Kingdom, Japan, Australia, South Korea, the GCC and across South-East Asia. All regulatory documents (DMF / CEP / LoA) and shipping incoterms (EXW, FCA, CIP, DAP, DDP) are negotiated per buyer.
Other peptides molecules from Longshine Boi-Tech's WHO-GMP catalogue — each with active regulatory filings, audit-ready CoA, and samples available under CDA.
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