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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino DS2 - Moligand™, ≥97% (HPLC) , Agonist of GABA A receptor δ; subunit, CAS No.374084-31-8, Agonist of GABA A receptor δ; subunit
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. ≥97%(HPLC) Synonyms
NS-05662 | 4-Chloro-N-[2-(2-thienyl)imidazo[1,2-a]pyridin-3-yl]benzamide | Q27077117 | BIM-0003182.P001 | EN300-7478430 | SR-01000493095 | 4-chloro-N-(2-thiophen-2-ylimidazo[1,2-a]pyridin-3-yl)benzamide | BDBM50457445 | HY-103520 | SCHEMBL19695349 | DTXSI
Storage
Conservare a 2-8°C, essiccato
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Why this grade Moligand™, ≥97% (HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservare a 2-8°C, essiccato Ships Ghiaccio umido 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.
Specifications Sinonimi
NS-05662 | 4-Chloro-N-[2-(2-thienyl)imidazo[1,2-a]pyridin-3-yl]benzamide | Q27077117 | BIM-0003182.P001 | EN300-7478430 | SR-01000493095 | 4-chloro-N-(2-thiophen-2-ylimidazo[1,2-a]pyridin-3-yl)benzamide | BDBM50457445 | HY-103520 | SCHEMBL19695349 | DTXSI
Specifiche e purezza
Moligand™, ≥97% (HPLC)
Meccanismi biochimici e fisiologici
Modulatore allosterico positivo dei recettori GABAA. Potenzia le correnti evocate dal GABA mediate dai recettori α4β3δ (EC50= 142 nM, in vitro). Mostra un profilo di selettività complesso, con selettività per i recettori contenenti δ (α4/6βxδ > α1βxδ >> γ
Condizioni di conservazione di stoccaggio
Conservare a 2-8°C, essiccato
Meccanismo d'azione
Agonist of GABA A receptor δ; subunit
Nomi e identificatori Sorrisi canonici
C1=CC2=NC(=C(N2C=C1)NC(=O)C3=CC=C(C=C3)Cl)C4=CC=CS4
IUPAC Name
4-chloro-N-(2-thiophen-2-ylimidazo[1,2-a]pyridin-3-yl)benzamide
InChIKey
AZKMWHRDICVYEI-UHFFFAOYSA-N
INCHI
1S/C18H12ClN3OS/c19-13-8-6-12(7-9-13)18(23)21-17-16(14-4-3-11-24-14)20-15-5-1-2-10-22(15)17/h1-11H,(H,21,23)
Isomeri SMILES
C1=CC2=NC(=C(N2C=C1)NC(=O)C3=CC=C(C=C3)Cl)C4=CC=CS4
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=28616507&ln=
Documentazione 📋 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 Kingdom Organic compounds Superclass Benzenoids Classe Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Halobenzoic acids and derivatives Direct Parent 4-halobenzoic acids and derivatives Alternative Parents Benzamides Imidazo[1,2-a]pyridines Imidazopyridines Benzoyl derivatives Chlorobenzenes Aryl chlorides Pyridines and derivatives N-substituted imidazoles Thiophenes Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organooxygen compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides Organochlorides Organonitrogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents 4-halobenzoic acid or derivatives - Imidazopyridine - Imidazo[1,2-a]pyridine - Benzamide - Benzoyl - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Pyridine - N-substituted imidazole - Thiophene - Imidazole - Heteroaromatic compound - Azole - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound Descrizione This compound belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Solubilità Solvent:DMSO, Max Conc. mg/mL: 17.69, Max Conc. mM: 50 Peso molecolare 353.800 g/mol XLogP3 4.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 353.039 Da Monoisotopic Mass 353.039 Da Topological Polar Surface Area 74.600 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 458.000 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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Reconstitution Calculator Recensioni Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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