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2-METHYL-8-(PHENYLMETHOXY)IMIDAZO[1,2-A]PYRIDINE-3-ACETONITRILE, also known as SCH 28080, is a reversible K+-competitive inhibitor of H+/K+-ATPases. It is best known for its ability to block acid secretion through its action against the gastric H+/K+-ATPase (IC50 = 1.3 μM). SCH 28080 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.

76081-98-6

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76081-98-6 Usage

Uses

Used in Pharmaceutical Industry:
2-METHYL-8-(PHENYLMETHOXY)IMIDAZO[1,2-A]PYRIDINE-3-ACETONITRILE is used as a potent inhibitor of H+,K+-ATPase for the treatment of gastric acid-related disorders. It works by blocking acid secretion in the stomach, providing relief from symptoms associated with excess stomach acid.
Used in Research Applications:
2-METHYL-8-(PHENYLMETHOXY)IMIDAZO[1,2-A]PYRIDINE-3-ACETONITRILE is used as a research tool to investigate the role of H+/K+-ATPases in various biological processes. It helps researchers understand the function and regulation of these enzymes in both mammalian and non-mammalian organisms.
Used in Drug Development:
2-METHYL-8-(PHENYLMETHOXY)IMIDAZO[1,2-A]PYRIDINE-3-ACETONITRILE is used as a lead compound in the development of new drugs targeting H+/K+-ATPases. Its unique mechanism of action and selectivity make it a valuable starting point for designing more effective and targeted therapies for acid-related disorders.

Biological Activity

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 .

Biochem/physiol Actions

SCH-28080 is a potent inhibitor of gastric H+ and K+-ATPase. The novel antiulcer agents, SCH-28080 and SCH-32651 were examined for their ability to inhibit the H+K+ ATPase enzyme activity in a preparation of microsomal membranes from rabbit fundic mucosa. SCH- 28080 inhibited the isolated enzyme activity with a potency similar to omeprazole, IC50s of 2.5 and 4.0 μM respectively. SCH 32651 was less potent exhibiting an IC50 of 200.0 μM. Both compounds may therefore exert their antisecretory activity via a direct inhibition of the parietal cell H+K+ ATPase.

Check Digit Verification of cas no

The CAS Registry Mumber 76081-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,8 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76081-98:
(7*7)+(6*6)+(5*0)+(4*8)+(3*1)+(2*9)+(1*8)=146
146 % 10 = 6
So 76081-98-6 is a valid CAS Registry Number.
InChI:InChI=1/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

76081-98-6 Well-known Company Product Price

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  • Sigma

  • (S4443)  SCH-28080  ≥98% (HPLC), solid

  • 76081-98-6

  • S4443-10MG

  • 1,755.00CNY

  • Detail
  • Sigma

  • (S4443)  SCH-28080  ≥98% (HPLC), solid

  • 76081-98-6

  • S4443-50MG

  • 7,833.15CNY

  • Detail

76081-98-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methyl-8-phenylmethoxyimidazo[1,2-a]pyridin-3-yl)acetonitrile

1.2 Other means of identification

Product number -
Other names -

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:76081-98-6 SDS

76081-98-6Relevant academic research and scientific papers

Skin Lightening Compositions

-

, (2011/08/02)

Compositions and methods for lightening and/or depigmenting skin are provided, the compositions comprising compounds having the structure: or having the structure: as defined herein.

IMIDAZO(1,2-a)(PYRIDAZINES OR PYRAZINES) FOR TREATMENT OF DISEASES RELATED TO BONE LOSS

-

, (2008/06/13)

A method for the treatment of diseases related to loss of bone mass such as osteoporosis, Paget's disease of bone, hy-perparathyroidism, malignant neoplasms causing hypercalcinemia, parodontal diseases and implant-related bone loss comprising administration to a patient suffering thereform an amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.

Antinuclear Agents. 1. Gastric Antisecretory and Cytoprotective Properties of Substituted Imidazopyridines

Kaminski, James J.,Bristol, James A.,Puchalski, Chester,Lovey, Raymond G.,Elliott, Arthur J.,et al.

, p. 876 - 892 (2007/10/02)

A novel class of antinuclear agents, the substituted imidazopyridines, is described.The present compounds are not histamine (H2) receptor antagonists nor are they prostaglandin analoques, yet they exhibit both gastric antisecretory and c

Imidazo[1,2-A]pyridines and use

-

, (2008/06/13)

This invention relates to imidazo[1,2-a]pyridine derivatives which are useful in the treatment of peptic ulcer diseases.

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