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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items AZ 12799734 - ≥98%(HPLC) , CAS No.1117684-36-2
Synonyms
BDBM35955 | 4-pyridinoxy-2-anilinopyridine-based compound, 19 | SCHEMBL373618 | 1117684-36-2 | 4-({4-[(2,6-Dimethylpyridin-3-yl)oxy]pyridin-2-yl}amino)benzenesulfonamide | Q27468118 | HY-123900 | EC-000.2535 | 2wou | H6YYY77937 | 4-[[4-[(2.6-Dimethyl-3-py
Shipped In
Hielera + almohadillas de hielo
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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 Conservar a -20°C Ships Hielera + almohadillas de hielo 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 Sinónimos
BDBM35955 | 4-pyridinoxy-2-anilinopyridine-based compound, 19 | SCHEMBL373618 | 1117684-36-2 | 4-({4-[(2, 6-Dimethylpyridin-3-yl)oxy]pyridin-2-yl}amino)benzenesulfonamide | Q27468118 | HY-123900 | EC-000.2535 | 2wou | H6YYY77937 | 4-[[4-[(2.6-Dimethyl-3-py
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Potente inhibidor del receptor del factor de crecimiento transformante-β tipo I (TGF-βRI; ALK5) (IC50= 17 nM en el ensayo de inhibición celular y 47 nM en el ensayo de actividad luciferasa inducida por TGF-β). También inhibe ALK4, ALK6 y ALK7 a concentrac
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Nombres e identificadores Sonrisas canónicas CC1=NC(=C(C=C1)OC2=CC(=NC=C2)NC3=CC=C(C=C3)S(=O)(=O)N)C IUPAC Name 4-[[4-(2,6-dimethylpyridin-3-yl)oxypyridin-2-yl]amino]benzenesulfonamide InChIKey UEOZXMAOIHDDQE-UHFFFAOYSA-N INCHI 1S/C18H18N4O3S/c1-12-3-8-17(13(2)21-12)25-15-9-10-20-18(11-15)22-14-4-6-16(7-5-14)26(19,23)24/h3-11H,1-2H3,(H,20,22)(H2,19,23,24) Isómeros SMILES CC1=NC(=C(C=C1)OC2=CC(=NC=C2)NC3=CC=C(C=C3)S(=O)(=O)N)C Peso molecular 370.43 Reaxy-Rn 18793116 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18793116&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 Organic oxygen compounds Clase Organooxygen compounds Subclass Ethers Intermediate Tree Nodes Not available Direct Parent Diarylethers Alternative Parents Benzenesulfonamides Benzenesulfonyl compounds Aniline and substituted anilines Methylpyridines Aminopyridines and derivatives Organosulfonamides Imidolactams Heteroaromatic compounds Aminosulfonyl compounds Secondary amines Azacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Diaryl ether - Benzenesulfonamide - Benzenesulfonyl group - Aniline or substituted anilines - Aminopyridine - Methylpyridine - Monocyclic benzene moiety - Pyridine - Imidolactam - Benzenoid - Organosulfonic acid amide - Heteroaromatic compound - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Azacycle - Organoheterocyclic compound - Secondary amine - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic nitrogen compound - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. 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.
Estructura 3D Objetivos asociados (humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:DMSO, Max Conc. mg/mL: 37.04, Max Conc. mM: 100 Peso molecular 370.400 g/mol XLogP3 2.600 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 5 Exact Mass 370.11 Da Monoisotopic Mass 370.11 Da Topological Polar Surface Area 116.000 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 545.000 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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