ZSET1446 - Moligand™, ≥98% , CAS No.887603-94-3

CAS: 887603-94-3 Cat. No.: Z647181 Formule: C15H12N2O Poids moléculaire: 236.27 PubChem CID: 10220323
DISPONIBLE À COMMANDE
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
A13764 | HY-11013 | spiro[1,3-dihydroindene-2,3'-imidazo[1,2-a]pyridine]-2'-one | BCP33073 | 1',3'-Dihydro-2H-spiro[imidazo[1,2-a]pyridine-3,2'-inden]-2-one | Q27268838 | ZSET-1446 | ST101 | SB18912
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Allemagne (EU)
USA*
Price
Qty
1mg
Z647181-1mg
—
5 En stock
63,26€
5mg
Z647181-5mg
—
3 En stock
143,96€
25mg
Z647181-25mg
—
3 En stock
381,72€
100mg
Z647181-100mg
—
1 En stock
734,02€
Enter a quantity for the sizes you want to add.
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Why this grade

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

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

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

Vue d’ensemble

ZSET1446 is a novel cognitive enhancer that significantly improves learning deficits in various types of Alzheimer disease (AD) models.

In Vitro

ZSET1446 (100 pM-10 nM) exerts limited effects on the basal neuronal excitability and synaptic transmission. ZSET1446 potentiates the facilitatory effect of nAChR stimulation on sPSC frequency. ZSET1446 potentiates the increase in sIPSC frequency by local application of nicotine (5 µM; 2 minutes) without affecting the basal sIPSC frequency at the range of 10 pM to 1 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

ZSET1446 enhances object recognition memory in mice and ameliorates cognitive impairment caused by scopolamine in rats. Concomitant administration of subeffective doses of ZSET1446 and memantine significantly ameliorates the cognitive performance in the novel object recognition task in both mice and rats. Moreover, oral administration of ZSET1446 or memantine increases the extracellular level of ACh in the hippocampus as compared with the control. Further, concomitant administration of subeffective doses of ZSET1446 and memantine significantly increases the extracellular level of ACh as compared with the group of ZSET1446 or memantine alone. ZSET1446 (0.002, 0.01, and 0.1 mg/kg, p.o.) ameliorates cognitive deficits of SAMP8 after 4, 8, 12, and 16 weeks of treatment in a novel object recognition test. ZSET1446 also reduces grading scores of SAMP8 after 16 weeks of treatment. Further, 8-week treatment of ZSET1446 significantly reduces the total number of Aβ-positive granules in the hippocampus. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal administration

The experimental apparatus consists of a Plexiglas open-field box [25 cm (width) × 41 cm (length) × 17 cm (depth), model TP-105], the floor of which is covered with sawdust. The apparatus is located in a sound-attenuated room. The procedure for the novel object recognition task consists of three different sessions: habituation, training, and retention sessions. Each mouse is individually habituated to the box, with 10 min of exploration in the absence of objects (day 1: habituation session). ZSET1446 at doses of 0.001, 0.003, 0.01, and 0.03 mg/kg and/or memantine at doses of 3 and 10 mg/kg is orally administered 60 min before the training trial. In the experiment of injection of nicotinic receptor antagonists, oral administration of ZSET1446 and i.p. injection of mechamylamine or DHbE at each dose of 1 mg/kg are given 60 min before the training trial. During the training session, two different novel objects are symmetrically fixed to the floor in the box, and each animal is allowed to explore in the box for 10 min (day 2: training session). These objects are different in shape and color but similar in size. The mice are considered to be exploring the object when the mouse is facing, touching, or sniffing the object. The time spent for exploring each object is manuallymeasured by a stopwatch. In the training session, locomotor activity is simultaneously measured for a period of 10 min automatically, using an Animex Auto placed under the open-field box. After the training trial, mice are immediately returned to their home cages. aladdin has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Specifications

Synonymes
A13764 | HY-11013 | spiro[1,3-dihydroindene-2,3'-imidazo[1,2-a]pyridine]-2'-one | BCP33073 | 1',3'-Dihydro-2H-spiro[imidazo[1,2-a]pyridine-3,2'-inden]-2-one | Q27268838 | ZSET-1446 | ST101 | SB18912
Spécifications et pureté
Moligand™, ≥98%
Mécanismes biochimiques et physiologiques
ZSET1446 is a novel cognitive enhancer that significantly improves learning deficits in various types of Alzheimer disease (AD) models.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Moligand™
Pureté
≥98%
Noms et identifiants
Pubchem Sid528768581
Sourires canoniquesC1C2=CC=CC=C2CC13C(=O)N=C4N3C=CC=C4
IUPAC Namespiro[1,3-dihydroindene-2,3'-imidazo[1,2-a]pyridine]-2'-one
InChIKeyQZWYXEBIQWJXAR-UHFFFAOYSA-N
INCHI1S/C15H12N2O/c18-14-15(17-8-4-3-7-13(17)16-14)9-11-5-1-2-6-12(11)10-15/h1-8H,9-10H2
Isomères SMILES C1C2=CC=CC=C2CC13C(=O)N=C4N3C=CC=C4
CAS alternatif 887603-94-3
PubChem CID 10220323
Termes d'entrée MeSH spiro(imidazo-(1,2-a)pyridine-3,2-indan)-2(3H)-one;ST 101;ST-101;ST101 cpd;ZSET 1446;ZSET1446
Poids moléculaire 236.27

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
ClasseImidazopyridines
SubclassImidazopyridinones
Intermediate Tree Nodes Not available
Direct ParentImidazopyridinones
Alternative Parents Alpha amino acids and derivatives  Indanes  Pyridinones  Dihydropyridines  Imidazolinones  N-acylimines  Propargyl-type 1,3-dipolar organic compounds  Enamines  Carboximidamides  Carboxamidines  Azacyclic compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Alpha-amino acid or derivatives - Imidazopyridinone - Indane - Dihydropyridine - Pyridinone - Imidazolinone - Benzenoid - 2-imidazoline - N-acylimine - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Enamine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Organic oxygen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as imidazopyridinones. These are compounds containing an imidazopyridine moiety where the pyridine ring bears a ketone group.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

4 results found

Lot NumberCertificate TypeDateArticle
H2508678Certificate of AnalysisApr 12, 2025 Z647181
H2508679Certificate of AnalysisApr 12, 2025 Z647181
H2508680Certificate of AnalysisApr 12, 2025 Z647181
H2508681Certificate of AnalysisApr 12, 2025 Z647181
Propriétés chimiques et physiques
SolubilitéDMSO : 50 mg/mL (211.62 mM; Need ultrasonic)
Poids moléculaire236.270 g/mol
XLogP31.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass236.095 Da
Monoisotopic Mass236.095 Da
Topological Polar Surface Area32.700 Ų
Heavy Atom Count18
Formal Charge0
Complexity475.000
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
Calculateurs de solution
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