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ChemicalBook >> CAS DataBase List >> NF 279

NF 279

NF 279 price.
  • $212 - $2065
  • Product name: NF 279
  • CAS: 202983-32-2
  • MF: C49H37N6NaO23S6
  • MW: 1293.2
  • EINECS:604-604-1
  • MDL Number:MFCD01861187
  • Synonyms:NF 279;8,8'-(CARBONYLBIS(IMINO-4,1-PHENYLENECARBONYLIMINO-4,1-PHENYLENECARBONYLIMINO))BIS-1,3,5-NAPHTHALENETRISULFONIC ACID, NA;8,8'-[CARBONYLBIS(IMINO-4,1-PHENYLENECARBONYLIMINO-4,1-PHENYLENECARBONYLIMINO)]BIS-1,3,5-NAPHTHALENETRISULFONIC ACID HEXASODIUM SALT;8,8[Carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-1,3,5-naphthalenetrisulfonicacidhex;8,8'-[Carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-1,3,5-naphthalene-trisulphonic acid hexasodium salt;8,8'-[Carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-1,3,5-naphthalenetrisulfonic acid;8,8'-[Carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-1,3,5-naphthalenetrisulfonic acid sodium salt;8,8'-[Carbonylbis(imino-4,1-phenylenecarbonylimino-4,1-phenylenecarbonylimino)]bis-1,3,5-naphthalenetrisulfonicacidhexasodiumsalt
Price8 Properties Safety Information Description
8 prices
Selected condition：
Brand
  • American Custom Chemicals Corporation
  • ApexBio Technology
  • Medical Isotopes, Inc.
  • Sigma-Aldrich
  • Tocris
  • TRC
  • Usbiological
Package
  • 10
  • 50
  • 5MG
  • 10mg
  • 50mg
  • 250mg
  • ManufacturerAmerican Custom Chemicals Corporation
  • Product numberAPI0009856
  • Product descriptionNF 279 95.00%
  • Packaging5MG
  • Price$505.15
  • Updated2021-12-16
  • Buy
  • ManufacturerApexBio Technology
  • Product numberB6629
  • Product descriptionNF279
  • Packaging50mg
  • Price$1290
  • Updated2021-12-16
  • Buy
  • ManufacturerMedical Isotopes, Inc.
  • Product number41692
  • Product descriptionNF279
  • Packaging10mg
  • Price$650
  • Updated2021-12-16
  • Buy
  • ManufacturerSigma-Aldrich
  • Product number480418
  • Product descriptionNF279 - CAS 202983-32-2 - Calbiochem
    A suramin analog that acts as a highly selective, competitive, and reversible ATP-antagonist of P2X receptor (IC /KB ~ 1 μM in smooth muscle).
  • Packaging5mg
  • Price$251
  • Updated2024-03-01
  • Buy
  • ManufacturerTocris
  • Product number1199
  • Product descriptionNF279 ≥95%(HPLC)
  • Packaging10
  • Price$212
  • Updated2021-12-16
  • Buy
  • ManufacturerTocris
  • Product number1199
  • Product descriptionNF279 ≥95%(HPLC)
  • Packaging50
  • Price$887
  • Updated2021-12-16
  • Buy
  • ManufacturerTRC
  • Product numberN391680
  • Product descriptionNF279
  • Packaging250mg
  • Price$2065
  • Updated2021-12-16
  • Buy
  • ManufacturerUsbiological
  • Product number255973
  • Product descriptionNF 279
  • Packaging10mg
  • Price$466
  • Updated2021-12-16
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
American Custom Chemicals Corporation API0009856 NF 279 95.00% 5MG $505.15 2021-12-16 Buy
ApexBio Technology B6629 NF279 50mg $1290 2021-12-16 Buy
Medical Isotopes, Inc. 41692 NF279 10mg $650 2021-12-16 Buy
Sigma-Aldrich 480418 NF279 - CAS 202983-32-2 - Calbiochem
A suramin analog that acts as a highly selective, competitive, and reversible ATP-antagonist of P2X receptor (IC /KB ~ 1 μM in smooth muscle). 		5mg $251 2024-03-01 Buy
Tocris 1199 NF279 ≥95%(HPLC) 10 $212 2021-12-16 Buy
Tocris 1199 NF279 ≥95%(HPLC) 50 $887 2021-12-16 Buy
TRC N391680 NF279 250mg $2065 2021-12-16 Buy
Usbiological 255973 NF 279 10mg $466 2021-12-16 Buy

Properties

storage temp. :Desiccate at -20°C
solubility :DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form :White solid
Water Solubility :Soluble to 25 mM in water
Stability :Hygroscopic

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

NF 279 is a suramin analog that acts as a highly selective, competitive, and reversible ATP-antagonist of P2X receptor (IC50/KB ~ 1 μM in smooth muscle). Effectively discriminates between P2Y and P2X receptors with no effect on α1A adrenoceptors, adenosine A1 and A2B receptors, histamine H1, muscarinic M3 and neuronal nicotinic acetylcholine receptors. Displays a selectivity profile of P2X1 >P2X2 >P2X3 >P2X4 (IC50 = 19 nM, 770 nM, 1.62 μM and >300 μM, respectively) in Xenopus oocytes pre-incubated with ATP. In rat and human tissues, exhibits a potency profile of rat P2X1 > human P2X1 > > rat P2X2 > rat P2X3 ~ human P2X7 > > human P2X4. Not degraded by ecto-nucleotidases.

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Suppliers and manufacturers

Career Henan Chemica Co
LEAPCHEM CO., LTD. 3B Pharmachem (Wuhan) International Co.,Ltd. AdooQ BioScience, LLC Jinan Mingya Medical Technology Co., Ltd. AdooQ Bioscience CHINA Sigma-Aldrich BOC Sciences Changzhou Chenhong Biotechnology Co., Ltd. Cckinase, Inc.