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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
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Indole alkaloid Property

storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
PXT0002558
Product name
ALSTONINE
Purity
95.00%
Packaging
5MG
Price
$498.96
Updated
2021/12/16
ChemScene
Product number
CS-0078920
Product name
Alstonine
Packaging
5mg
Price
$1200
Updated
2021/12/16
Arctom
Product number
CFN97709
Product name
Alstonine
Purity
≥98%
Packaging
5mg
Price
$448
Updated
2021/12/16
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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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Indole alkaloid Suppliers

Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
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China
ProdList
6011
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BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Fax
0871-65215563
Email
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Country
China
ProdList
5654
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Sichuan Wei Keqi Biological Technology Co., Ltd.
Tel
028-81700200 18116577057
Fax
028-81705658
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3003855609@qq.com
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China
ProdList
7892
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ALB Technology Limited
Tel
702-983-3769
Fax
702-983-3769
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sales@albtechnology.com
Country
United States
ProdList
2993
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Wuhan ChemFaces Biochemical Co., Ltd.
Tel
18607101326 15172504745
Fax
+86-27-84254680
Email
aileen@chemfaces.com
Country
China
ProdList
7059
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EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8449
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Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
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China
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Shanghai ChengShao Biological Technology Co., Ltd.
Tel
021-61847300 13341622919
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China
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Beijing Jin Ming Biotechnology Co., Ltd.
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010-60605840 18892239720
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12308
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Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
400-400-400-9004166 18616739031
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Country
China
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52712
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642-18-2, Indole alkaloidRelated Search:


  • 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)-
  • 642-18-2