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· · COA & SDS available for every product · Same-day shipping on in-stock items LAU463 - Moligand™ , Allosteric modulator of GABA A receptor α6 subunit, CAS No.L611460, Allosteric modulator of GABA A receptor α6 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. Synonyms
7-Bromo-2,5-dihydro-2-(4-methoxyphenyl)-3H-pyrazolo[4,3-c]quinolin-3-one | compound 8n [PMID: 29481759] | GTPL12405 | SCHEMBL18285404 | 2055050-88-7 | DTXSID901150239 | LAU463
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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 Synonyms
7-Bromo-2, 5-dihydro-2-(4-methoxyphenyl)-3H-pyrazolo[4, 3-c]quinolin-3-one | compound 8n [PMID: 29481759] | GTPL12405 | SCHEMBL18285404 | 2055050-88-7 | DTXSID901150239 | LAU463
Specifications & Purity
Moligand™
Action Type
ALLOSTERIC MODULATOR
Mechanism of action
Allosteric modulator of GABA A receptor α6 subunit
Names and Identifiers Canonical Smiles COC1=CC=C(C=C1)N2N=C3C(=CNC4=C3C=CC(Br)=C4)C2=O InChIKey CAJJWNTVLDPILI-UHFFFAOYSA-N INCHI 1S/C17H12BrN3O2/c1-23-12-5-3-11(4-6-12)21-17(22)14-9-19-15-8-10(18)2-7-13(15)16(14)20-21/h2-9,19H,1H3 Isomeric SMILES COC1=CC=C(C=C1)N2C(=O)C3=CN=C4C=C(C=CC4=C3N2)Br PubChem CID 124111379
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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Quinolines and derivatives Subclass Quinoline carboxamides Intermediate Tree Nodes Not available Direct Parent Quinoline-3-carboxamides Alternative Parents Phenylpyrazoles Haloquinolines Pyrazolopyridines Phenoxy compounds Methoxybenzenes Anisoles Tetrahydropyridines Methylpyridines Alkyl aryl ethers Pyrazolones Vinylogous amides Heteroaromatic compounds Lactams Amino acids and derivatives Vinyl bromides Dialkylamines Bromoalkenes Azacyclic compounds Organopnictogen compounds Organobromides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Quinoline-3-carboxamide - Haloquinoline - Phenylpyrazole - Pyrazolopyridine - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - Methylpyridine - Tetrahydropyridine - Alkyl aryl ether - Benzenoid - Pyridine - Pyrazolinone - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous amide - Pyrazoline - Pyrazole - Azole - Lactam - Amino acid or derivatives - Azacycle - Bromoalkene - Haloalkene - Vinyl halide - Vinyl bromide - Secondary amine - Ether - Secondary aliphatic amine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Amine - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as quinoline-3-carboxamides. These are quinolines in which the quinoline ring system is substituted by one carboxamide group at the 3-position. 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews 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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