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Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
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
| Pubchem Sid | 528768581 |
|---|---|
| Sonrisas canónicas | C1C2=CC=CC=C2CC13C(=O)N=C4N3C=CC=C4 |
| IUPAC Name | spiro[1,3-dihydroindene-2,3'-imidazo[1,2-a]pyridine]-2'-one |
| InChIKey | QZWYXEBIQWJXAR-UHFFFAOYSA-N |
| INCHI | 1S/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 |
| Isómeros SMILES | C1C2=CC=CC=C2CC13C(=O)N=C4N3C=CC=C4 |
| CAS alternativo | 887603-94-3 |
| PubChem CID | 10220323 |
| Términos de entrada MeSH | spiro(imidazo-(1,2-a)pyridine-3,2-indan)-2(3H)-one;ST 101;ST-101;ST101 cpd;ZSET 1446;ZSET1446 |
| Peso molecular | 236.27 |
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Imidazopyridines |
| Subclass | Imidazopyridinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Imidazopyridinones |
| 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 Framework | Aromatic 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 |
| Descripción | This 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 12, 2025 | Z647181 | |
| Certificate of Analysis | Apr 12, 2025 | Z647181 | |
| Certificate of Analysis | Apr 12, 2025 | Z647181 | |
| Certificate of Analysis | Apr 12, 2025 | Z647181 |
| Solubilidad | DMSO : 50 mg/mL (211.62 mM; Need ultrasonic) |
|---|---|
| Peso molecular | 236.270 g/mol |
| XLogP3 | 1.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 236.095 Da |
| Monoisotopic Mass | 236.095 Da |
| Topological Polar Surface Area | 32.700 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 475.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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