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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock BQCA - ≥98%(HPLC) , CAS No.338747-41-4
Synonyms
HY-101858 | 1-(4-methoxybenzyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid | MLS000755157 | HMS2641J10 | 1-(4-Methoxy-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid | 1-(4-methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | MFCD01315710
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) 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 BQCA a highly selective allosteric modulator of the M1 mAChR.
Specifications Synonymes
HY-101858 | 1-(4-methoxybenzyl)-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid | MLS000755157 | HMS2641J10 | 1-(4-Methoxy-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid | 1-(4-methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | MFCD01315710
Spécifications et pureté
≥98%(HPLC)
Mécanismes biochimiques et physiologiques
Muscarinic M1receptor positive allosteric modulator (pKB5.76 - 5.82). Exhibits selectivity for M1over M3and M5receptors. Enhances ACh effects at M1receptors in an IP1- accumulation assay, without affecting ACh binding. Increases markers of neuronal activa
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.
Noms et identifiants Pubchem Sid 504760504 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504760504 Sourires canoniques COC1=CC=C(C=C1)CN2C=C(C(=O)C3=CC=CC=C32)C(=O)O IUPAC Name 1-[(4-methoxyphenyl)methyl]-4-oxoquinoline-3-carboxylic acid InChIKey BZBBTGCKPRSPGF-UHFFFAOYSA-N INCHI 1S/C18H15NO4/c1-23-13-8-6-12(7-9-13)10-19-11-15(18(21)22)17(20)14-4-2-3-5-16(14)19/h2-9,11H,10H2,1H3,(H,21,22) Isomères SMILES COC1=CC=C(C=C1)CN2C=C(C(=O)C3=CC=CC=C32)C(=O)O WGK Allemagne 3 Poids moléculaire 309.32 Reaxy-Rn 12911382 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12911382&ln=
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 Classe Quinolines and derivatives Subclass 1-benzylquinolines Intermediate Tree Nodes Not available Direct Parent 1-benzylquinolines Alternative Parents Quinoline carboxylic acids Hydroquinolones Hydroquinolines Pyridinecarboxylic acids Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Vinylogous amides Heteroaromatic compounds Carboxylic acids Azacyclic compounds Monocarboxylic acids and derivatives Organonitrogen compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents 1-benzylquinoline - Quinoline-3-carboxylic acid - Dihydroquinolone - Dihydroquinoline - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Methoxybenzene - Anisole - Phenol ether - Phenoxy compound - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Pyridine - Heteroaromatic compound - Vinylogous amide - Azacycle - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as 1-benzylquinolines. These are organic aromatic compounds containing a quinoline that is substituted at the 1-position by a benzyl group. 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Solvent:DMSO, Max Conc. mg/mL: 6.19, Max Conc. mM: 20 with gentle warming Poids moléculaire 309.300 g/mol XLogP3 3.400 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 309.1 Da Monoisotopic Mass 309.1 Da Topological Polar Surface Area 66.800 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 493.000 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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