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10245-81-5

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10245-81-5 Usage

Description

Pentabromopseudilin is a metabolite derived from Chromobacterium, a bacterium found in a seawater sample from the North Pacific Gyre. It exhibits significant antibiotic properties and is known to play a role in autoinhibition within the Chromobacterium itself.

Uses

Used in Pharmaceutical Industry:
Pentabromopseudilin is used as an antibiotic agent for its antibiotic action against various types of bacteria. The compound has demonstrated the ability to inhibit bacterial growth, making it a potential candidate for the development of new antibiotics to combat bacterial infections.
Used in Research and Development:
Pentabromopseudilin is also used as a research tool to study the mechanisms of autoinhibition in Chromobacterium and other similar bacteria. Understanding these mechanisms can provide insights into bacterial behavior and contribute to the development of targeted therapies and treatments for bacterial infections.

Check Digit Verification of cas no

The CAS Registry Mumber 10245-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10245-81:
(7*1)+(6*0)+(5*2)+(4*4)+(3*5)+(2*8)+(1*1)=65
65 % 10 = 5
So 10245-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H4Br5NO/c11-3-1-4(9(17)5(12)2-3)8-6(13)7(14)10(15)16-8/h1-2,16-17H

10245-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibromo-6-(3,4,5-tribromo-1H-pyrrol-2-yl)phenol

1.2 Other means of identification

Product number -
Other names 2,4-dibromo-6-(3,4,5-tribromo-pyrrol-2-yl)-phenol

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:10245-81-5 SDS

10245-81-5Relevant articles and documents

Two-step total synthesis of an anti-MRSA and myosin-inhibiting marine natural product pentabromopseudilin via Suzuki-Miyaura coupling of a MIDA boronate ester

Kum, Dong-Young,Nazari, Mohamad,McPhail, Kerry L.,Cooper, Christina S.,Suyama, Takashi L.

, p. 3374 - 3376 (2017)

A marine natural product isolated from Pseudoalteromonas sp., pentabromopseudilin, with promising anti-MRSA and myosin ATPase inhibition activities was synthesized in two steps using recently developed MIDA boronate Suzuki-Miyaura coupling technology. Add

Silver(I)-catalyzed route to pyrroles: Synthesis of halogenated pseudilins as allosteric inhibitors for myosin atpase and x-ray crystal structures of the protein-inhibitor complexes

Martin, Rene,Risacher, Celia,Barthel, Andre,Jaeger, Anne,Schmidt, Arndt W.,Richter, Sabine,Boehl, Markus,Preller, Matthias,Chinthalapudi, Krishna,Manstein, Dietmar J.,Gutzeit, Herwig O.,Knoelker, Hans-Joachim

, p. 4487 - 4505 (2014/08/05)

The pentahalogenated 2-arylpyrrole-type alkaloids pentabromopseudilin and pentachloropseudilin represent a new class of isoform-specific allosteric inhibitors of myosin ATPase. Herein, we describe an application of the silver(I)-catalyzed cycloisomerizati

MEANS FOR TREATING MYOSIN-RELATED DISEASES

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Page/Page column 16-17, (2011/05/08)

The present invention provides a method of designing a modulator of a myosin, the method comprising molecular modeling of a compound such that the modeled compound interacts with at least three amino acid residues of said myosin, said residues being selec

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