SCH 28080 - ≥98% , CAS No.76081-98-6

CAS: 76081-98-6 Cat. No.: S286840 Peso molecular: 277.33 PubChem CID: 108137
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
LP00439 | S28080 | Lopac-S-4443 | NCGC00015953-01 | NCGC00015953-03 | S 4443 | SCH28080 | Sch-28080 | FT-0641585 | SDCCGSBI-0050424.P002 | (8-Benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-yl)-acetonitrile | (8-Benzyloxy-2-methylimidazo[1,2-a]pyridin-3-yl)ace
Storage
Conservar a -20°C
Shipped In
Hielera + almohadillas de hielo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
S286840-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
61,90US$
5mg
S286840-5mg
2
219,90US$
10mg
S286840-10mg
2
349,90US$
25mg
S286840-25mg
2
787,90US$
50mg
S286840-50mg
2
1.399,90US$
100mg
S286840-100mg
2
2.379,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservar a -20°C Ships Hielera + almohadillas de hielo Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Descripción del producto

SCH28080 es un inhibidor reversible, K+-competitivo de la H,K-ATPasa gástrica, con un Ki de 0,12 μM. El SCH28080 es un inhibidor eficaz de la secreción ácida in vivo y con actividad antiúlcera gástrica.


Aplicacióndel producto

El SCH-28080 se utilizó en el tratamiento de embriones de pez cebra para estudiar el papel de la H+/K+-ATPasa en el establecimiento del eje izquierda-derecha durante el desarrollo.


Specifications

Sinónimos
LP00439 | S28080 | Lopac-S-4443 | NCGC00015953-01 | NCGC00015953-03 | S 4443 | SCH28080 | Sch-28080 | FT-0641585 | SDCCGSBI-0050424.P002 | (8-Benzyloxy-2-methyl-imidazo[1, 2-a]pyridin-3-yl)-acetonitrile | (8-Benzyloxy-2-methylimidazo[1, 2-a]pyridin-3-yl)ace
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Potente inhibidor de la H+, K+-ATPasa (IC50= 20 nM); se une al sitio de reconocimiento del K+ y es competitivo con respecto al K+. Inhibe la secreción ácida gástrica in vitroe in vivo.
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Tipo de acción
INHIBITOR
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasCC1=C(N2C=CC=C(C2=N1)OCC3=CC=CC=C3)CC#N
IUPAC Name2-(2-methyl-8-phenylmethoxyimidazo[1,2-a]pyridin-3-yl)acetonitrile
InChIKeyPYKJFEPAUKAXNN-UHFFFAOYSA-N
INCHI1S/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
Isómeros SMILES CC1=C(N2C=CC=C(C2=N1)OCC3=CC=CC=C3)CC#N
WGK Alemania 3
PubChem CID 108137
Peso molecular 277.33

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseImidazopyridines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentImidazopyridines
Alternative Parents Imidazo[1,2-a]pyridines  Alkyl aryl ethers  Pyridines and derivatives  N-substituted imidazoles  Benzene and substituted derivatives  Heteroaromatic compounds  Nitriles  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Imidazopyridine - Imidazo[1,2-a]pyridine - Alkyl aryl ether - Monocyclic benzene moiety - N-substituted imidazole - Pyridine - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Nitrile - Carbonitrile - Ether - Azacycle - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as imidazopyridines. These are organic polycyclic compounds containing an imidazole ring fused to a pyridine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CYP1A2 Tchem Cytochrome P450 1A2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ARSA Tbio Cerebroside-sulfatase (655 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsomes (16955 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATP4A Tclin Potassium-transporting ATPase (493 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SHMT2 Tchem Serine hydroxymethyltransferase, mitochondrial (242 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATP4A Potassium-transporting ATPase alpha chain 1 (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Schistosoma mansoni (6170 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sus scrofa (849 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeFechaArticulo
G2307949Certificate of AnalysisApr 07, 2026 S286840
G2307951Certificate of AnalysisApr 07, 2026 S286840
G2307952Certificate of AnalysisApr 07, 2026 S286840
G2307953Certificate of AnalysisApr 07, 2026 S286840
G2307954Certificate of AnalysisApr 07, 2026 S286840
K2527043Certificate of AnalysisMay 30, 2023 S286840
Propiedades químicas y físicas
SolubilidadSolvent:ethanol, Max Conc. mg/mL: 2.77, Max Conc. mM: 10; Solvent:DMSO, Max Conc. mg/mL: 6.93, Max Conc. mM: 25
Peso molecular277.320 g/mol
XLogP33.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass277.122 Da
Monoisotopic Mass277.122 Da
Topological Polar Surface Area50.300 Ų
Heavy Atom Count21
Formal Charge0
Complexity385.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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