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52659-57-1

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  • 2,6,10,17-Tetraoxatricyclo[11.3.1.11,5]octadecane-7,11-dione,3-[(1S,4S)-4-(2-bromo-5-hydroxyphenyl)-4-methoxy-1-methylbutyl]-13-hydroxy-9-[(1R)-1-hydroxyethyl]-4,14,16,16-tetramethyl-,(1S,3R,4S,5S,9R,

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  • 2,6,10,17-Tetraoxatricyclo[11.3.1.11,5]octadecane-7,11-dione,3-[(1S,4S)-4-(2-bromo-5-hydroxyphenyl)-4-methoxy-1-methylbutyl]-13-hydroxy-9-[(1R)-1-hydroxyethyl]-4,14,16,16-tetramethyl-,(1S,3R,4S,5S,9R,

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  • 2,6,10,17-Tetraoxatricyclo[11.3.1.11,5]octadecane-7,11-dione,3-[(1S,4S)-4-(2-bromo-5-hydroxyphenyl)-4-methoxy-1-methylbutyl]-13-hydroxy-9-[(1R)-1-hydroxyethyl]-4,14,16,16-tetramethyl-,(1S,3R,4S,5S,9R,

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52659-57-1 Usage

Description

Aplysiatoxin, a cyanotoxin, is the parent member of the class of aplysiatoxins. It is produced by various species of freshwater and marine cyanobacteria, as well as algae and molluscs. Aplysiatoxin possesses potent biological activities and has been a subject of interest for its potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
Aplysiatoxin is used as a pharmaceutical compound for its potent biological activities. It has been studied for its potential applications in the development of new drugs, particularly in the areas of cancer treatment and other therapeutic applications. The toxin's unique properties make it a promising candidate for the creation of novel therapeutic agents.
Used in Research and Development:
Aplysiatoxin is used as a research tool in the field of biochemistry and pharmacology. Its potent biological activities and complex structure make it an interesting subject for studying the mechanisms of action and potential applications in drug development. Researchers utilize aplysiatoxin to better understand the interactions between toxins and biological systems, which can lead to the discovery of new therapeutic targets and strategies.
Used in Environmental Monitoring:
Aplysiatoxin is used as a biomarker for monitoring the presence of harmful cyanobacteria and algae in freshwater and marine environments. The detection of aplysiatoxin can indicate the presence of toxic species, which can pose risks to human health and the ecosystem. Monitoring aplysiatoxin levels can help in the early detection of harmful algal blooms and inform appropriate management actions to protect public health and the environment.

Hazard

A poison.

Safety Profile

poison by intraperitoneal route.Mutation data reported. When heated to decomposition itemits toxic vapors of Br-??.

Check Digit Verification of cas no

The CAS Registry Mumber 52659-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,5 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52659-57:
(7*5)+(6*2)+(5*6)+(4*5)+(3*9)+(2*5)+(1*7)=141
141 % 10 = 1
So 52659-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C32H47BrO10/c1-17(8-11-24(39-7)22-12-21(35)9-10-23(22)33)29-19(3)26-15-32(42-29)30(5,6)14-18(2)31(38,43-32)16-28(37)40-25(20(4)34)13-27(36)41-26/h9-10,12,17-20,24-26,29,34-35,38H,8,11,13-16H2,1-7H3/t17-,18+,19-,20+,24-,25+,26-,29+,31-,32-/m0/s1

52659-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name aplysiatoxin

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:52659-57-1 SDS

52659-57-1Upstream product

52659-57-1Downstream Products

52659-57-1Relevant articles and documents

Absolute Stereochemistries of the Aplysiatoxins and Oscillatoxin A

Moore, Richard E.,Blackman, Adrian J.,Cheuk, Chad E.,Mynderse, Jon S.,Matsumoto, Gayle K.,et al.

, p. 2484 - 2489 (2007/10/02)

Optical and proton NMR spectral studies of the aplysiatoxins and derivatives, degradation products of the toxins and an X-ray crystallographic analysis of 19,21-dibromoaplysiatoxin show that the absolute configurations of the ten asymmetric carbons are 3S,4R,7S,9S,10S,11R,12S,15S,29R,30R.The 31-nor compound, oscillatoxin A, has the same absolute stereochemistry at C(3), C(4), C(7), C(9), C(10), C(11), C(12), C(15), and C(29).

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