Indole alkaloid
- Product Name
- Indole alkaloid
- CAS No.
- 642-18-2
- Chemical Name
- Indole alkaloid
- Synonyms
- Aids002662;Aids-002662;3,4,5,6,16,17-Hexadehydro-16-(methoxycarbonyl)-19.alpha.-methyl-20.alpha.- oxayohimbanium;Oxayohimbanium,3,4,5,6,16,17-hexadehydro-16-(methoxycarbonyl)-19-methyl-, inner salt, (19a,20a)-
- CBNumber
- CB92493188
- Molecular Formula
- C21H20N2O3
- Formula Weight
- 348.4
- MOL File
- 642-18-2.mol
Indole alkaloid Property
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- form
- Solid
- color
- White to yellow
N-Bromosuccinimide Price
- Product number
- PXT0002558
- Product name
- ALSTONINE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $498.96
- Updated
- 2021/12/16
- Product number
- CS-0078920
- Product name
- Alstonine
- Packaging
- 5mg
- Price
- $1200
- Updated
- 2021/12/16
- Product number
- CFN97709
- Product name
- Alstonine
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $448
- Updated
- 2021/12/16
Indole alkaloid Chemical Properties,Usage,Production
Definition
ChEBI: Alstonine is an indole alkaloid with formula C21H20N2O3, isolated from several Rauvolfia species and exhibits antipsychotic activity. It has a role as an antipsychotic agent. It is a methyl ester, an organic heteropentacyclic compound, a zwitterion and an indole alkaloid. It is a conjugate base of an alstonine(1+).
Biological Activity
Alstonine is the main indole alkaloid compound of a botanical drug. Alstonine has antipsychotic, anxiolytic, anticancer and antimalarial properties.
in vitro
Alstonine has the capacity to distinguish cancer DNA from healthy tissue DNA; it inhibits DNA in vitro synthesis when DNA from different cancerous tissues or cells is used as template. Practically without effects on DNA from healthy tissues.
in vivo
In mice models Alstonine shows a clear, dose-dependent, potent antipsychotic profile. Alstonine (ip) prevents amphetamine-induced lethality, with active doses within the range of 0.5-2.0 mg/kg.
Alstonine (0.1, 0.5 and 1.0 mg/kg) prevents MK-801 induced hyperlocomotion. Because Alstonine partially reverses MK-801-induced increase in locomotion both at the hole-board and locomotor activity cages.
Alstonine successfully treats a relatively important proportion of BALB/C mice inoculated with transplantable YC8 lymphoma ascites cells as well as Swiss mice bearing Ehrlich ascites carcinoma cells.
Indole alkaloid Preparation Products And Raw materials
Raw materials
Preparation Products
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