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Biperiden Hydrochloride (KL 373 Hydrochloride) is an anticholinergic antiparkinsonian agent that selectively blocks central M1 cholinoreceptors while exerting atropine-like effects on peripheral parasympathetic structures. Biperiden Hydrochloride is approved for the adjunctive treatment of postencephalitic, idiopathic, and arteriosclerotic Parkinson’s disease, demonstrates minimal impairment of novelty preference compared with other anticholinergics in comparative cognitive studies, and is associated with known adverse effects including drowsiness, vertigo, headache, and dizziness.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | $558 | 35 days | 35 days | |
| 50 mg | $2,370 | 35 days | 35 days |
| Description | Biperiden Hydrochloride (KL 373 Hydrochloride) is an anticholinergic antiparkinsonian agent that selectively blocks central M1 cholinoreceptors while exerting atropine-like effects on peripheral parasympathetic structures. Biperiden Hydrochloride is approved for the adjunctive treatment of postencephalitic, idiopathic, and arteriosclerotic Parkinson’s disease, demonstrates minimal impairment of novelty preference compared with other anticholinergics in comparative cognitive studies, and is associated with known adverse effects including drowsiness, vertigo, headache, and dizziness. |
| In vitro | In human pancreatic ductal adenocarcinoma cell lines (Panc-1, Panc-2, and BxPC3), treatment with Biperiden Hydrochloride (29.6 μg/mL) for 72 hours inhibited cell proliferation and induced apoptosis [1]. |
| In vivo | In a subcutaneous xenograft mouse model using Panc-1 pancreatic cancer cells, intraperitoneal administration of Biperiden Hydrochloride (10 mg/kg, Daily) for 3 weeks resulted in an 83% reduction in tumor size via MALT1 inhibition [4]. Separately, in a pilocarpine-induced epilepsy model, Biperiden treatment (8 mg/kg, i.p., every 8 hours) for 10 days modified the progression of epileptogenesis. It reduced the frequency of spontaneous recurrent seizures and lowered extracellular glutamate levels in the hippocampus, leading to a long-term decrease in hippocampal excitability [5]. |
| Synonyms | KL-373 Hydrochloride, KL373 Hydrochloride, KL 373 Hydrochloride |
| Molecular Weight | 347.92 |
| Formula | C21H30ClNO |
| Cas No. | 1235-82-1 |
| Smiles | Cl.OC(C=1C=CC=CC1)(CCN2CCCCC2)C3CC4C=CC3C4 |
| Relative Density. | 1.31g/cm3 |
| Storage | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| Solubility Information | DMSO: 2.6 mg/mL (7.47 mM), Sonication is recommended. H2O: 5 mg/mL (14.37 mM), Sonication is recommended. | |||||||||||||||||||||||||
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H2O
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