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NF 279 is a suramin analog that functions as a highly selective, competitive, and reversible ATP-antagonist of the P2X receptor. It effectively differentiates between P2Y and P2X receptors without impacting other receptors such as α1A adrenoceptors, adenosine A1 and A2B receptors, histamine H1, muscarinic M3, and neuronal nicotinic acetylcholine receptors. NF 279 exhibits a selectivity profile of P2X1 > P2X2 > P2X3 > P2X4 and is not degraded by ecto-nucleotidases.

202983-32-2

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202983-32-2 Usage

Uses

Used in Pharmaceutical Industry:
NF 279 is used as a potent and selective P2X1 antagonist for the development of therapeutic agents targeting the P2X1 receptor. Its high selectivity and potency make it a valuable compound for research and drug development in various conditions where the P2X1 receptor plays a significant role.
Used in Smooth Muscle Research:
In smooth muscle, NF 279 is used as a selective antagonist for studying the role of P2X receptors in muscle contraction and relaxation. Its IC50/KB value of approximately 1 μM makes it a useful tool for investigating the underlying mechanisms of smooth muscle function and potential therapeutic applications.
Used in Xenopus Oocytes Expression System:
NF 279 is used as a selective antagonist in the Xenopus oocytes pre-incubated with ATP to study the selectivity profile of P2X1, P2X2, P2X3, and P2X4 receptors. This application aids in understanding the receptor interactions and their roles in various physiological processes.
Used in Rat and Human Tissue Studies:
NF 279 is used to investigate the potency profile of rat P2X1, human P2X1, rat P2X2, rat P2X3, human P2X7, and human P2X4 receptors in rat and human tissues. This helps researchers to comprehend the differences in receptor activity and potential species-specific therapeutic approaches.

Biological Activity

A potent and selective P2X 1 antagonist (IC 50 = 19 nM). Displays good selectivity over P2X 2 ,(IC 50 = 0.76 μ M), P2X 3 (IC 50 = 1.62 μ M), P2X 4 (IC 50 > 300 μ M), P2Y receptors and ecto-nucleotidases.

Biochem/physiol Actions

Cell permeable: yes

Check Digit Verification of cas no

The CAS Registry Mumber 202983-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,9,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 202983-32:
(8*2)+(7*0)+(6*2)+(5*9)+(4*8)+(3*3)+(2*3)+(1*2)=122
122 % 10 = 2
So 202983-32-2 is a valid CAS Registry Number.

202983-32-2SDS

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 N-[4,6,8-tris(methylsulfonyl)naphthalen-1-yl]-4-[[4-[[4-[[4-[[4,6,8-tris(methylsulfonyl)naphthalen-1-yl]carbamoyl]phenyl]carbamoyl]phenyl]carbamoylamino]benzoyl]amino]benzamide

1.2 Other means of identification

Product number -
Other names NF 279

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:202983-32-2 SDS

202983-32-2Upstream product

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