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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock 852A - Moligand™ , Toll-like receptor 7 agonist, CAS No.A607276, Toll-like receptor 7 agonist
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
GTPL9025 | MS-25728 | N-(4-(4-Amino-2-ethyl-imidazo(4,5-c)quinolin-1-yl)butyl)methanesulfonamide | SCHEMBL483385 | HY-100176 | N-(4-(4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl)methanesulfonamide | N-(4-{4-AMINO-2-ETHYL-1H-IMIDAZO[4,5-C]QUINOLIN-
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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 Synonymes
GTPL9025 | MS-25728 | N-(4-(4-Amino-2-ethyl-imidazo(4,5-c)quinolin-1-yl)butyl)methanesulfonamide | SCHEMBL483385 | HY-100176 | N-(4-(4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl)methanesulfonamide | N-(4-{4-AMINO-2-ETHYL-1H-IMIDAZO[4,5-C]QUINOLIN-
Spécifications et pureté
Moligand™
Conditions de stockage de stockage
Room temperature
Mécanisme d'action
Toll-like receptor 7 agonist
Noms et identifiants Sourires canoniques CCc1nc2c(n1CCCCNS(=O)(=O)C)c1ccccc1nc2N IUPAC Name N-[4-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)butyl]methanesulfonamide InChIKey YZOQZEXYFLXNKA-UHFFFAOYSA-N INCHI 1S/C17H23N5O2S/c1-3-14-21-15-16(12-8-4-5-9-13(12)20-17(15)18)22(14)11-7-6-10-19-25(2,23)24/h4-5,8-9,19H,3,6-7,10-11H2,1-2H3,(H2,18,20) Isomères SMILES CCC1=NC2=C(N1CCCCNS(=O)(=O)C)C3=CC=CC=C3N=C2N PubChem CID 10309114
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 Imidazoquinolines Intermediate Tree Nodes Not available Direct Parent Imidazoquinolines Alternative Parents Aminoquinolines and derivatives Imidazo-[4,5-c]pyridines Aminopyridines and derivatives Organosulfonamides Organic sulfonamides N-substituted imidazoles Imidolactams Benzenoids Heteroaromatic compounds Aminosulfonyl compounds Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Imidazoquinoline - Aminoquinoline - Imidazopyridine - Imidazo-[4,5-c]pyridine - Aminopyridine - N-substituted imidazole - Pyridine - Organic sulfonic acid amide - Imidolactam - Benzenoid - Organosulfonic acid amide - Azole - Imidazole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Azacycle - Organosulfur compound - Organonitrogen compound - Hydrocarbon derivative - Primary amine - Organic oxygen compound - Amine - Organic nitrogen compound - Organic oxide - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as imidazoquinolines. These are aromatic heterocyclic compounds containing an imidazole ring fused to a quinoline ring system. In some configurations, the imidazole ring shares a nitrogen atom with the quinoline moiety. 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 Poids moléculaire 361.500 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 7 Exact Mass 361.157 Da Monoisotopic Mass 361.157 Da Topological Polar Surface Area 111.000 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 538.000 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 Avis 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 → Produits apparentés SM 324405 - ≥98%(HPLC) , CAS No.677773-91-0
DSR 6434 - ≥98%(HPLC) , CAS No.1059070-10-8
TLR7 agonist T7 - ≥98% , CAS No.1062444-54-5
TLR7 agonist 2 - 10mM in DMSO , CAS No.1642857-69-9
TLR7 agonist 1 - 10mM in DMSO , CAS No.2178156-33-5
TLR7/8 agonist 3 - 10mM in DMSO , CAS No.642473-95-8
TLR7/8 agonist 1 - 10mM in DMSO , CAS No.1258457-59-8
TLR7 agonist 3 - 10mM in DMSO , CAS No.1229024-78-5
TLR7/8/9-IN-1 - ≥99% , CAS No.2180127-82-4
TLR7 agonist 1 - ≥98% , CAS No.2178156-33-5
TLR7/8 agonist 3 - ≥99% , CAS No.642473-95-8
TLR7/8 agonist 1 - ≥96% , CAS No.1258457-59-8
TLR7/8-IN-1 - ≥99% , CAS No.2205095-75-4
TLR7 agonist 2 - ≥99% , CAS No.1642857-69-9
TLR7 agonist 3 - ≥98% , CAS No.1229024-78-5
TLR7/8 agonist 4 - 10mM in DMSO , CAS No.2388520-33-8
MC-Val-Cit-PAB-Amide-TLR7 agonist 4 , CAS No.2413016-49-4
TLR7/8 agonist 1 dihydrochloride - ≥99% , CAS No.1620278-72-9
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