Nootropics Powders Huperzine a CAS 102518-79-6
|FOB Unit Price:||US $1 US $0.78|
|Purchase Qty. (g)||FOB Unit Price|
|Production Capacity:||2 Tons/Year|
|Transport Package:||1 Kg/Foil Bag|
|Payment Terms:||T/T, Western Union, Money Gram, Bitcoin|
- Model NO.: Huperzine A
- Customized: Customized
- Suitable for: Adult
- Purity: >99%
- Alias: Huperzine a
- Einecs No: 120786-18-7
- Molecular Weight: 242.32
- Trademark: YC
- Origin: Hubei, China
- Powder: Yes
- Certification: GMP, HSE, ISO 9001
- State: Solid
- Product Name: Huperzine a
- CAS Registry Number: 120786-18-7
- Molecular Formula: C15h18n2o
- Appearance: White Powder
- Specification: USD Standard
- HS Code: 3001200010
|Product Name||Huperzine A|
|CAS Registry Number||120786-18-7|
Synonyms: (+/-)-SELAGINE;[+/-]-SELAGINE;SELAGINE;(+/-)-HUPERAZINE A;HUPERAZINE A;(+/-)-HUPERZINE A;HUPERZINE A;(+/-)-Selagine
Product Categories: Natural Plant Extract;Acetylcholine receptor;Herb extract
Mol File: 120786-18-7.mol
Huperzine A Structure
Huperzine A, used in middle and old aged patients with benign memory disorders and various types of dementia, cognitive function and emotional behavior disorders. Can be used for the treatment of myasthenia gravis.
This product is a reversible inhibitor of choline zymase, selective inhibition of acetylcholinesterase. High biological activity, high fat soluble, small, easily through the blood-brain barrier, enters the central mostly distributed in the brain's frontal, temporal lobe, hippocampus and other brain areas associated with learning and memory, in a low dose of acetylcholinesterase (AChE) inhibition is strong, so the distribution area of synaptic gap of acetylcholine (ACh) content increased, thereby enhancing neuronal excitability conduction, strengthen the excitatory effect of learning and memory of brain regions, to improve cognitive function, enhance memory retention and promote the recovery of memory function. Animal experiments show that the oral absorption of this product is rapid and complete, bioavailability of 96%, 10-30 minutes up to peak plasma concentration, distribution is also fast, easy to pass the blood-brain barrier. Elimination half-life of 4 hours. Mainly through the urine in the form of the original and metabolites excreted in vitro, 24 hours to discharge the amount of 73.6%.
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