Tirzepatide (CAS 2023788-19-2) is a GMP-compliant, high-purity dual GIP/GLP-1 receptor agonist peptide API. FDA-approved for type 2 diabetes glycemic control and chronic weight management, it delivers robust glucose-lowering and sustained weight loss efficacy. It fully meets ICH, USP and EP standards for injectable pharmaceutical R&D and commercial manufacturing.
Atropine Sulfate (CAS 5908-99-6) is a GMP-compliant, high-purity anticholinergic active pharmaceutical ingredient (API). With potent muscarinic receptor blocking activity, it is widely used in antispasmodic, anti-bradycardia, ophthalmic mydriasis and organophosphate poisoning rescue, fully complying with USP/EP/CP pharmacopoeia standards.
Benzgalantamine Gluconate (CAS 1542321-58-3) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a prodrug of galantamine and reversible acetylcholinesterase inhibitor. With low gastrointestinal side effects and proven cognitive-improving efficacy, it is FDA-approved for treating mild-to-moderate Alzheimer's dementia, meeting global pharmaceutical quality standards.
Cilostazol (CAS 73963-72-1) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a selective phosphodiesterase 3 (PDE3) inhibitor with dual antiplatelet and vasodilatory effects. Globally approved for intermittent claudication from peripheral arterial disease, it fully meets USP/EP/CP pharmacopoeia standards.
Dotinurad (CAS 1285572-51-1) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a highly selective URAT1 inhibitor that suppresses renal uric acid reabsorption. Approved in Japan for hyperuricemia and gout treatment, it delivers potent urate-lowering efficacy with favorable safety, fully complying with ICH and global pharmacopoeia standards.
Edoxaban (CAS 1229194-11-9) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a selective direct factor Xa inhibitor oral anticoagulant. Globally approved for stroke prevention in non-valvular atrial fibrillation and venous thromboembolism treatment & prevention, it fully meets ICH, USP and EP pharmacopoeia standards.
Ertugliflozin L-Pyroglutamic Acid (CAS 1210344-83-4) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a highly selective SGLT2 inhibitor. By blocking renal glucose reabsorption, it delivers robust glycemic control, globally approved for type 2 diabetes mellitus treatment, fully meeting ICH, USP and EP pharmacopoeia quality standards.
Esaxerenone (CAS 1632006-28-0) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a highly selective non-steroidal mineralocorticoid receptor antagonist (MRA). Approved in Japan for primary hypertension and type 2 diabetic nephropathy treatment, it delivers robust antihypertensive efficacy with reduced endocrine side effects, fully complying with ICH, JP and USP pharmacopoeia standards.
Galantamine Hydrobromide (CAS 1953-04-4) is a GMP-compliant, high-purity active pharmaceutical ingredient (API), a reversible, centrally selective acetylcholinesterase inhibitor. Globally approved for mild-to-moderate Alzheimer's dementia cognitive improvement, it fully meets USP/EP/CP and ICH international quality standards.
Lemborexant (CAS 1369764-02-2) is a high-purity, GMP-compliant dual orexin receptor antagonist (DORA) API. It is clinically indicated for the treatment of insomnia disorder in adults, improving sleep onset and maintenance with favorable next‑day residual effects. It complies with ICH, USP and EP pharmacopoeial standards.
Mirogabalin Besylate (CAS 1138245-21-2) is a GMP-compliant, high-purity API, a selective α2δ-1 ligand of voltage-gated calcium channels. Approved for peripheral neuropathic pain (diabetic peripheral neuropathic pain & postherpetic neuralgia), it delivers sustained analgesia with favorable CNS safety, meeting ICH, JP, and USP pharmacopoeial standards.
Olmesartan Medoxomil (CAS 144689-63-4) is a high-purity, GMP-grade angiotensin II receptor antagonist (ARB) API. It is indicated for the treatment of hypertension, providing long-lasting blood pressure control with good tolerability. It meets USP, EP, and ICH quality standards, suitable for pharmaceutical formulation development and commercial production.
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