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1192750-33-6

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1192750-33-6 Usage

Uses

PE 154 is a potent and fluorescent inhibitor of human acetylcholinesterase

Check Digit Verification of cas no

The CAS Registry Mumber 1192750-33-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,7,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1192750-33:
(9*1)+(8*1)+(7*9)+(6*2)+(5*7)+(4*5)+(3*0)+(2*3)+(1*3)=156
156 % 10 = 6
So 1192750-33-6 is a valid CAS Registry Number.

1192750-33-6 Well-known Company Product Price

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  • Sigma

  • (SML0624)  PE 154  ≥97% (HPLC)

  • 1192750-33-6

  • SML0624-10MG

  • 2,315.43CNY

  • Detail
  • Sigma

  • (SML0624)  PE 154  ≥97% (HPLC)

  • 1192750-33-6

  • SML0624-50MG

  • 9,014.85CNY

  • Detail

1192750-33-6SDS

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 2-(4-(((7-(diethylamino)-2,4-dioxo-2H-chromen-3(4H)-ylidene)methyl)amino)phenyl)-N'-1,2,3,4-tetrahydroacridin-9-ylacetohydrazide

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:1192750-33-6 SDS

1192750-33-6Downstream Products

1192750-33-6Relevant articles and documents

A Gorge-spanning, High-affinity cholinesterase inhibitor to explore β-amyloid plaques

Elsinghorst, Paul W.,Haertig, Wolfgang,Goldhammer, Simone,Grosche, Jens,Guetschow, Michael

, p. 3940 - 3946 (2009)

Cholinesterases are involved in the pathological formation of β-amyloid plaques. To investigate this pathohistological hallmark of Alzheimer's disease we prepared a high-affinity, fluorescent cholinesterase inhibitor. Its fluorescence intensity was significantly enhanced upon binding to cholinesterases. Using this probe, brain samples from mice and humans affected by Alzheimer's disease were successfully analyzed for β-amyloid plaques. Unexpectedly, it was discovered, by competition experiments, that the compound binds to amyloid structures, rather than to cholinesterases inside of the plaques.

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