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Details

Stereochemistry ACHIRAL
Molecular Formula C17H15N3O
Molecular Weight 277.3205
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SCH-28080

SMILES

CC1=C(CC#N)N2C=CC=C(OCC3=CC=CC=C3)C2=N1

InChI

InChIKey=PYKJFEPAUKAXNN-UHFFFAOYSA-N
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

HIDE SMILES / InChI

Molecular Formula C17H15N3O
Molecular Weight 277.3205
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/2993001

SCH-28080 is an inhibitor of H+, K+-ATPase. Administration of SCH-28080 led to significant reduction in the volume, acid output and peptic activity of gastric secretions in a clinical trial.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.12 µM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Stable expression of gastric proton pump activity at the cell surface.
2002-06
Functional expression of the cDNA encoded by the human ATP1AL1 gene.
1996-09
Patents

Patents

Sample Use Guides

In a clinical trial, SCH-28080 was administered intragastrically via the tube as a 50 ml suspension at dosages of 50 - 200 mg.
Route of Administration: Intragastric
In Vitro Use Guide
Increasing concentrations of SCH 28080 inhibited the H + K + ATPase activity in a preparation of rabbit microsomal membranes. Compound didn't affect the basal (Mg 2+ only) enzyme activity at concentrations as high as 100 uM.
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:52:12 GMT 2025
Edited
by admin
on Mon Mar 31 17:52:12 GMT 2025
Record UNII
00427X161I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IMIDAZO(1,2-A)PYRIDINE-3-ACETONITRILE, 2-METHYL-8-(PHENYLMETHOXY)-
Preferred Name English
SCH-28080
Code English
2-METHYL-8-(PHENYLMETHOXY)IMIDAZO(1,2-A)-PYRIDINE-3-ACETONITRILE
Systematic Name English
SCH28080
Code English
Code System Code Type Description
CAS
76081-98-6
Created by admin on Mon Mar 31 17:52:12 GMT 2025 , Edited by admin on Mon Mar 31 17:52:12 GMT 2025
PRIMARY
PUBCHEM
108137
Created by admin on Mon Mar 31 17:52:12 GMT 2025 , Edited by admin on Mon Mar 31 17:52:12 GMT 2025
PRIMARY
FDA UNII
00427X161I
Created by admin on Mon Mar 31 17:52:12 GMT 2025 , Edited by admin on Mon Mar 31 17:52:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID10226971
Created by admin on Mon Mar 31 17:52:12 GMT 2025 , Edited by admin on Mon Mar 31 17:52:12 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY