2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile

2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile Struktur
76081-98-6
CAS-Nr.
76081-98-6
Englisch Name:
2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile
Synonyma:
SCH 28080;S28080;SCH-28080,SCH28080;Schering compound 28080;SCH28080, 10 mM in DMSO;imidazo-(1-2-a)pyrine-3-acetonitrile;2-Methyl-8-(phenylmethoxy)imidazo-(1-2-A)pyrine-3-acetonitrile;2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile;2-(8-(Benzyloxy)-2-methylimidazo[1,2-a]pyridin-3-yl)acetonitrile;Imidazo(1,2-A)pyridine-3-acetonitrile, 2-methyl-8-(phenylmethoxy)-
CBNumber:
CB4281209
Summenformel:
C17H15N3O
Molgewicht:
277.32
MOL-Datei:
76081-98-6.mol

2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile Eigenschaften

Dichte
1.16±0.1 g/cm3(Predicted)
storage temp. 
-20°C
Löslichkeit
DMSO: >10 mg/mL, soluble
Aggregatzustand
solid
pka
5.85±0.10(Predicted)
Farbe
white to light tan
InChI
1S/C17H15N3O/c1-13-15(9-10-18)20-11-5-8-16(17(20)19-13)21-12-14-6-3-2-4-7-14/h2-8,11H,9,12H2,1H3
InChIKey
PYKJFEPAUKAXNN-UHFFFAOYSA-N
SMILES
Cc1nc2c(OCc3ccccc3)cccn2c1CC#N

Sicherheit

S-Sätze: 22-24/25
WGK Germany  3
Speicherklasse 11 - Combustible Solids

2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Beschreibung

SCH 28080 is a reversible K+-competitive inhibitor of H+/K+-ATPases that is best known for its ability to block acid secretion through its action against the gastric H+/K+-ATPase (IC50 = 1.3 μM). It is effective against gastric H+/K+-ATPases from a variety of species and can inhibit colonic H+/K+-ATPases, but this activity appears to be species-dependent. SCH 28080 is also used to investigate the role of H+/K+-ATPases in non-mammalian organisms and to distinguish the actions of H+/K+-ATPases from other ATP-dependent transporters.

Verwenden

SCH 28080 is a potent inhibitor of H+,K+-ATPase.

Biologische Aktivität

Potent inhibitor of H + ,K + -ATPase (IC 50 = 20 nM); binds to the K + recognition site and is competitive with respect to K + . Inhibits gastric acid secretion in vitro and in vivo .

2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 76)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037
3bsc@sina.com China 15813 69
Bide Pharmatech Ltd. 400-164-7117 18317119277
product02@bidepharm.com China 40000 60
Sigma-Aldrich 021-61415566 800-8193336
orderCN@merckgroup.com China 51389 80
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266
China 4862 55
EMMX Biotechnology LLC 888-539-0666
info@emmx.com United States 8435 60
Shanghai YuanYe Biotechnology Co., Ltd. 18916372613
yanzihan@shyuanye.com China 87240 60
Shanghai Chaolan Chemical Technology Center QQ:65489617 13301690235
Sales@ATKchemical.com China 9808 58
TargetMol Chemicals Inc. +1-781-999-5354; +1-00000000000
marketing@targetmol.com United States 32431 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767
sales@chemegen.com China 11123 58
Suzhou Chenrui Biotechnology Co. LTD 17625585511
1580084073@qq.com China 994 58

  • 3-(CYANOMETHYL)-2-METHYL-8-(PHENYLMETHOXY)IMIDAZO[1,2-ALPHA]PYRIDINE
  • 2-Methyl-8-(phenylmethoxy)imidazo-(1-2-A)pyrine-3-acetonitrile
  • Imidazo(1,2-A)pyridine-3-acetonitrile, 2-methyl-8-(phenylmethoxy)-
  • S28080
  • Schering compound 28080
  • imidazo-(1-2-a)pyrine-3-acetonitrile
  • SCH-28080,SCH28080
  • 2-(8-(Benzyloxy)-2-methylimidazo[1,2-a]pyridin-3-yl)acetonitrile
  • SCH28080, 10 mM in DMSO
  • SCH 28080
  • 2-Methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile
  • 76081-98-6
  • Ion Pump Inhibitors
  • Ion Channels
  • Monovalent Ion Channels
  • Voltage-gated Ion Channels
  • BioChemical
  • Cell Signaling and Neuroscience
  • Cell Biology
  • ATPase
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