Welcome to LookChem.com Sign In|Join Free
  • or
Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[3-(4-nitrophenoxy)propyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143665-30-9

Post Buying Request

143665-30-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

143665-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143665-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,6 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143665-30:
(8*1)+(7*4)+(6*3)+(5*6)+(4*6)+(3*5)+(2*3)+(1*0)=129
129 % 10 = 9
So 143665-30-9 is a valid CAS Registry Number.

143665-30-9Relevant academic research and scientific papers

Synthesis, electrophysiological properties and analysis of structural requirements of a novel class of antiarrhythmic agents with potassium and calcium channel blocking properties

Nadler, Guy,Faivre, Jean-Francois,Forest, Marie-Claire,Cheval, Brigitte,Martin, Michel,Souchet, Michel,Gout, Bernard,Bril, Antoine

, p. 1993 - 2011 (2007/10/03)

Class III antiarrhythmic agents have been shown to prevent reentrant arrhythmias but also to be responsible for initiating arrhythmias characterised by afterdepolarizations and triggered activities. By combining potassium and calcium channel antagonistic

Synthesis and Activity against Multidrug Resistance in Chinese Hamster Ovary Cells of New Acridone-4-carboxamides

Dodic, Nerina,Dumaitre, Bernard,Daugan, Alain,Pianetti, Pascal

, p. 2418 - 2426 (2007/10/02)

A number of tricyclic carboxamides have been synthesized and tested to evaluate their ability to reverse multidrug resistance in the CHRC/5 cell line.Among them the acridone derivatives were the most potent.A key feature is the presence of a dimethoxybenzyl or phenethylamine cationic site, separated from the tricyclic lipophilic part by a carbamoylphenyl chain.Optimization led to compounds 2 orders of magnitude more active than the prototype inhibitors verapamil and amiodarone.On the basis of in vitro and in vivo activities, 9,10-dihydro-5-methoxy-9-oxo-N-phenyl>-4-acridinecarboxamide (84) has been selected for further development.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 143665-30-9