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627034-85-9,MFCD03791135
Catalog No.:AA00EETC

627034-85-9 | NF449

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1mg
≥95%
in stock  
$53.00   $37.00
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5mg
≥95%
in stock  
$129.00   $90.00
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10mg
≥95%
in stock  
$230.00   $161.00
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50mg
≥95%
in stock  
$1,006.00   $704.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00EETC
Chemical Name:
NF449
CAS Number:
627034-85-9
Molecular Formula:
C41H24N6Na8O29S8
Molecular Weight:
1505.0902
MDL Number:
MFCD03791135
SMILES:
O=C(Nc1cc(cc(c1)C(=O)Nc1ccc(cc1S(=O)(=O)[O-])S(=O)(=O)[O-])C(=O)Nc1ccc(cc1S(=O)(=O)[O-])S(=O)(=O)[O-])Nc1cc(cc(c1)C(=O)Nc1ccc(cc1S(=O)(=O)[O-])S(=O)(=O)[O-])C(=O)Nc1ccc(cc1S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
Properties
Computed Properties
 
Complexity:
2890  
Covalently-Bonded Unit Count:
6  
Formal Charge:
-3  
Heavy Atom Count:
89  
Hydrogen Bond Acceptor Count:
29  
Hydrogen Bond Donor Count:
6  
Rotatable Bond Count:
10  

Literature

Title: Activation of transmembrane bile acid receptor TGR5 stimulates insulin secretion in pancreatic β cells.

Journal: Biochemical and biophysical research communications 20121026

Title: Effect of development on [Ca2+]i transients to ATP in petrosal ganglion neurons: a pharmacological approach using optical recording.

Journal: Journal of applied physiology (Bethesda, Md. : 1985) 20120415

Title: Molecular basis of selective antagonism of the P2X1 receptor for ATP by NF449 and suramin: contribution of basic amino acids in the cysteine-rich loop.

Journal: British journal of pharmacology 20120101

Title: Prostaglandin E2 induces spontaneous rhythmic activity in mouse urinary bladder independently of efferent nerves.

Journal: British journal of pharmacology 20120101

Title: Study of the reversal effect of NF449 on neuromuscular blockade induced by d-tubocurarine.

Journal: Life sciences 20110606

Title: Ionotropic NMDA and P2X1/5 receptors mediate synaptically induced Ca2+ signalling in cortical astrocytes.

Journal: Cell calcium 20101001

Title: NF449 is a novel inhibitor of fibroblast growth factor receptor 3 (FGFR3) signaling active in chondrocytes and multiple myeloma cells.

Journal: The Journal of biological chemistry 20100702

Title: Low doses of bisphenol A promote human seminoma cell proliferation by activating PKA and PKG via a membrane G-protein-coupled estrogen receptor.

Journal: Environmental health perspectives 20090701

Title: Bradykinin inhibits the transient outward K+ current in mouse Schwann cells via the cAMP/PKA pathway.

Journal: American journal of physiology. Cell physiology 20090601

Title: Spontaneous purinergic neurotransmission in the mouse urinary bladder.

Journal: The Journal of physiology 20081201

Title: Ectodomain lysines and suramin block of P2X1 receptors.

Journal: The Journal of biological chemistry 20081031

Title: Characterization of pharmacologically active compounds that inhibit poliovirus and enterovirus 71 infectivity.

Journal: The Journal of general virology 20081001

Title: Genistein potentiates protein kinase A activity in porcine coronary artery.

Journal: Molecular and cellular biochemistry 20080401

Title: Inhibition of human and mouse plasma membrane bound NTPDases by P2 receptor antagonists.

Journal: Biochemical pharmacology 20071115

Title: Primary and secondary agonists can use P2X(1) receptors as a major pathway to increase intracellular Ca(2+) in the human platelet.

Journal: Journal of thrombosis and haemostasis : JTH 20070501

Title: P2X purinergic receptor-mediated ionic current in cardiac myocytes of calsequestrin model of cardiomyopathy: implications for the treatment of heart failure.

Journal: American journal of physiology. Heart and circulatory physiology 20070201

Title: Histamine decreases myogenic tone in rat cerebral arteries by H2-receptor-mediated KV channel activation, independent of endothelium and cyclic AMP.

Journal: European journal of pharmacology 20061010

Title: Mechanisms of disease: role of purinergic signaling in the pathophysiology of bladder dysfunction.

Journal: Nature clinical practice. Urology 20060401

Title: Inhibition of platelet functions and thrombosis through selective or nonselective inhibition of the platelet P2 receptors with increasing doses of NF449 [4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis-(carbonylimino)))tetrakis-benzene-1,3-disulfonic acid octasodium salt].

Journal: The Journal of pharmacology and experimental therapeutics 20050701

Title: Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist.

Journal: Neuropharmacology 20050301

Title: Progesterone upregulates calcitonin gene-related peptide and adrenomedullin receptor components and cyclic adenosine 3'5'-monophosphate generation in Eker rat uterine smooth muscle cell line.

Journal: Biology of reproduction 20050201

Title: Structure-activity relationships of analogues of NF449 confirm NF449 as the most potent and selective known P2X1 receptor antagonist.

Journal: European journal of medicinal chemistry 20040401

Title: ATP-induced ATP release from astrocytes.

Journal: Journal of neurochemistry 20040101

Title: NF449, a novel picomolar potency antagonist at human P2X1 receptors.

Journal: European journal of pharmacology 20030530

Title: Development of Gs-selective inhibitory compounds.

Journal: Methods in enzymology 20020101

Title: NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors.

Journal: Naunyn-Schmiedeberg's archives of pharmacology 20010901

Title: Induction of Galphas contributes to the paradoxical stimulation of cytosolic phospholipase A2alpha expression by cortisol in human amnion fibroblasts.

Journal: Molecular endocrinology (Baltimore, Md.)

Title: Rettinger J, et al. Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist. Neuropharmacology. 2005;48(3):461-468.

Title: Hohenegger M, et al. Gsalpha-selective G protein antagonists. Proc Natl Acad Sci U S A. 1998;95(1):346-351.

Title: Hechler B, et al. Inhibition of platelet functions and thrombosis through selective or nonselective inhibition of the platelet P2 receptors with increasing doses of NF449 ,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis-(carbonylimino)))tetrakis-benzene-1,3-disulfonic acid octasodium salt J Pharmacol Exp Ther. 2005;314(1):232-243.

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