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CAS RN: 4429-63-4 | Product Number: T3500
Tabersonine
Purity: >98.0%(T)(HPLC)
Synonyms:
- Methyl 5α,12β,19α-2,3,6,7-Tetradehydroaspidospermidine-3-carboxylate
- Methyl (3aR,3a1S,10bR)-3a-Ethyl-3a,3a1,4,6,11,12-hexahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
250MG |
€ 248,00
|
1 | 22 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | T3500 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__2__1H__2__4N__2O__2 = 336.44 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Light Sensitive,Air Sensitive,Heat Sensitive |
Packaging and Container | 250MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 4429-63-4 |
Reaxys Registry Number | 50163 |
MDL Number | MFCD28140545 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Volumetric Analysis) | min. 98.0 % |
Melting point | 89.0 to 93.0 °C |
NMR | confirm to structure |
Properties (reference)
Melting Point | 91 °C |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H302 : Harmful if swallowed. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P270 : Do not eat, drink or smoke when using this product. P264 : Wash skin thoroughly after handling. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. |
Related Laws:
EC Number | 224-615-0 |
RTECS# | CJ0150000 |
Transport Information:
HS Number | 2939799090 |
Application
Tabersonine: An Indole Alkaloid with Neuroprotective Properties
Tabersonine is an indole alkaloid found in the beans of Voacanga africana, a plant traditionally used for religious purposes in Africa. There are reports that tabersonine exhibits specific and synergistic multiple neuroprotective properties, including inhibition of amyloid beta (Aβ) fibril-induced cytotoxicity.1,2) Tabersonine is also an intermediate in the biological and chemical synthesis of indole alkaloids, including the anticancer agent vincristine [V0129].1,3,4) (The product is for research purpose only.)
References
- 1) Tabersonine Inhibits Amyloid Fibril Formation and Cytotoxicity of Aβ(1-42)
- 2) Natural spirocyclic alkaloids and polyphenols as multi target dementia leads (a review)
- 3) Completion of the seven-step pathway from tabersonine to the anticancer drug precursor vindoline and its assembly in yeast
- 4) Vincamine by synthesis and semi-synthesis (a review)
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