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[5aR,(+)]-14aβ-(1,1-Dimethyl-2-propenyl)-5aβ,13aα,14,14a-tetrahydroindolo[3',2':4,5]pyrrolo[2,1-c][1,4]benzodiazepine-7,13(5H,12H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81797-27-5

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81797-27-5 Usage

Uses

Used in Pharmaceutical Industry:
[5aR,(+)]-14aβ-(1,1-Dimethyl-2-propenyl)-5aβ,13aα,14,14a-tetrahydroindolo[3',2':4,5]pyrrolo[2,1-c][1,4]benzodiazepine-7,13(5H,12H)-dione is used as a potential therapeutic agent for various medical conditions due to its diverse biological activities. Its alkaloid nature and unique chemical structure make it a promising candidate for the development of new drugs and treatments.
Used in Research and Development:
In the field of scientific research, [5aR,(+)]-14aβ-(1,1-Dimethyl-2-propenyl)-5aβ,13aα,14,14a-tetrahydroindolo[3',2':4,5]pyrrolo[2,1-c][1,4]benzodiazepine-7,13(5H,12H)-dione serves as a valuable compound for studying its pharmacological properties and exploring its potential applications in medicine. Further research is required to gain a comprehensive understanding of its medicinal properties and to develop effective drug formulations.
Used in Plant Biology and Ethnobotany:
As a compound derived from the plant Catharanthus roseus, [5aR,(+)]-14aβ-(1,1-Dimethyl-2-propenyl)-5aβ,13aα,14,14a-tetrahydroindolo[3',2':4,5]pyrrolo[2,1-c][1,4]benzodiazepine-7,13(5H,12H)-dione is also used in the study of plant biology and ethnobotany. It provides insights into the chemical composition and medicinal properties of plants, contributing to the understanding of traditional uses and potential modern applications of plant-derived compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 81797-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,9 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81797-27:
(7*8)+(6*1)+(5*7)+(4*9)+(3*7)+(2*2)+(1*7)=165
165 % 10 = 5
So 81797-27-5 is a valid CAS Registry Number.

81797-27-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ASZONALENIN

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:81797-27-5 SDS

81797-27-5Downstream Products

81797-27-5Relevant academic research and scientific papers

Stereospecific synthesis of aszonalenins by using two recombinant prenyltransferases

Yin, Wen-Bing,Cheng, Jun,Li, Shu-Ming

, p. 2202 - 2207 (2009)

In previous studies, two prenyltransferases were overproduced and characterised biochemically. AnaPT from Neosartorya fischeri is involved in the biosynthesis of acetylaszonalenin and was shown to catalyse the C3-prenylation of (R)-benzodiazepinedione (6)

Ir-catalyzed reverse prenylation of 3-substituted indoles: Total synthesis of (+)-aszonalenin and (-)-brevicompanine B

Ruchti, Jonathan,Carreira, Erick M.

, p. 16756 - 16759 (2015/02/02)

The selective reverse prenylation of 3-substituted-1H-indoles at C3 is described. The iridium-catalyzed reaction proceeds with high branched to linear selectivity (>20:1) for a variety of indoles. In addition, a diastereoselective reverse prenylation of tryptophan methyl ester is disclosed, and its synthetic utility is demonstrated in the synthesis of (+)-aszonalenin and (-)-brevicompanine B.

The biosynthesis of the mould metabolites roquefortine and aszonalenin from L-[2,4,5,6,7-2H5]tryptophan

Bhat,Harrison,Lamont

, p. 10663 - 10668 (2007/10/02)

L-[2,4,5,6,7-2H5]Tryptophan was incorporated into roquefortine 2 by Penicillium roqueforti and aszonalenin 3 by Aspergillus zonatus with retention in each case of five deuterium atoms; the 5a-hydrogen of both metabolites is derived from the 2-hydrogen of tryptophan.

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