Cyclogalegigenin CAS 84605-18-5
Chemical Name: Cyclogalegigenin
CAS No.: 84605-18-5
Molecular Formula: C30H50O5
Molecular Weight: 490.71
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Description
Cyclogalegigenin Details
Chemical Name: Cyclogalegigenin
CAS No.: 84605-18-5
Molecular Formula: C30H50O5
Molecular Weight: 490.71
Molecular?Structure:
Appearance: Powder
Cyclogalegigenin Typical Properties
Melting point
>220??C (dec.)
Boiling point
617.2??55.0 ??C(Predicted)
Density
1.20
Storage
Refrigerator
Appearance
Powder
Colour
White
Cyclogalegigenin Usage
Used for content determination/identification/experiments, etc.
Cyclogalegigenin Packaging and Shipping
Packing: 25KG/Drum
Cyclogalegigenin Storage
Keep in a well-closed,?light-resistant, dry and cool place.
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- 2-diallylpent-4-en-1-amine
- 4
- 95-16-9
- Ammonium sulfamate
- Benzothiazole
- cas:67889-00-3ح2
- cas:83524-75-8 | pigment black 32
- cas:928836-00-4 | 2
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- Chemical Minerals
- Coconut diethanolamide
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- discount
- for sale
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- hexyl D-glucoside
- in stock
- Lauramidopropyl betaine
- LAURIC ACID MONOETHANOLAMIDE
- Petroleum Additives
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- Ploymers
- price
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- Raw Materal
- Remove term: Petroleum Additives Petroleum Additive
- SODIUM ETHYL 2-SULFOLAURATE
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Huperzine A is a natural plant extract. Compared with similar AD treatment drugs approved by the US FDA, Huperzine A has a unique chemical structure and has extremely high selectivity to inhibit acetylcholinesterase in the brain and enhance cholinergic in the brain. function of neurons. In addition, Huperzine A has obvious effects on improving memory and improving cognitive ability.
Huperzine A has a small relative molecular weight, high lipid solubility, and is easy to pass through the blood-brain barrier. After entering the central nervous system, it is mostly distributed in the frontal lobe, temporal lobe, hippocampus and other parts of the brain. Its pharmacological effects have multiple targets. In addition to inhibiting the activity of acetylcholinesterase, it can also antagonize oxidative stress and apoptosis induced by ??-amyloid peptide (A??), hydrogen peroxide and other neurotoxins, by activating the protein kinase C (PKC) signal transduction pathway. Activation of ??-secretase promotes the decomposition of ??-amyloid precursor protein (APP) in a non-amyloidogenic manner to produce sAPP??, reducing A??-mediated toxicity, while sAPP?? can effectively promote cell proliferation, axonal growth, and protect nerves. cell.


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