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· · COA & SDS available for every product · Same-day shipping on in-stock items SX-517 - Moligand™ , Antagonist of CXCR2, CAS No.S614275, Antagonist of CXCR2
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
HY-12927 | AKOS040749589 | (2-(((5-((4-Fluorophenyl)carbamoyl)pyridin-2-yl)thio)methyl)phenyl)boronic acid | 36UH926WTQ | 1240494-13-6 | SCHEMBL13197143 | [2-[[5-[(4-fluorophenyl)carbamoyl]pyridin-2-yl]sulfanylmethyl]phenyl]boronic acid | Boronic acid, B-
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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
HY-12927 | AKOS040749589 | (2-(((5-((4-Fluorophenyl)carbamoyl)pyridin-2-yl)thio)methyl)phenyl)boronic acid | 36UH926WTQ | 1240494-13-6 | SCHEMBL13197143 | [2-[[5-[(4-fluorophenyl)carbamoyl]pyridin-2-yl]sulfanylmethyl]phenyl]boronic acid | Boronic acid, B-
Specifications & Purity
Moligand™
Mechanism of action
Antagonist of CXCR2
Names and Identifiers Canonical Smiles Fc1ccc(cc1)NC(=O)c1ccc(nc1)SCc1ccccc1B(O)O IUPAC Name [2-[[5-[(4-fluorophenyl)carbamoyl]pyridin-2-yl]sulfanylmethyl]phenyl]boronic acid InChIKey VZRIHFZJVIOJBE-UHFFFAOYSA-N INCHI 1S/C19H16BFN2O3S/c21-15-6-8-16(9-7-15)23-19(24)13-5-10-18(22-11-13)27-12-14-3-1-2-4-17(14)20(25)26/h1-11,25-26H,12H2,(H,23,24) Isomeric SMILES B(C1=CC=CC=C1CSC2=NC=C(C=C2)C(=O)NC3=CC=C(C=C3)F)(O)O PubChem CID 46897162
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 Benzenoids Class Benzene and substituted derivatives Subclass Anilides Intermediate Tree Nodes Not available Direct Parent Aromatic anilides Alternative Parents Nicotinamides Alkylarylthioethers Fluorobenzenes Aryl fluorides Heteroaromatic compounds Secondary carboxylic acid amides Boronic acids Sulfenyl compounds Azacyclic compounds Organic metalloid salts Organofluorides Organometalloid compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organooxygen compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Aromatic anilide - Nicotinamide - Pyridine carboxylic acid or derivatives - Aryl thioether - Fluorobenzene - Halobenzene - Alkylarylthioether - Aryl halide - Aryl fluoride - Pyridine - Heteroaromatic compound - Boronic acid derivative - Boronic acid - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Sulfenyl compound - Carboxylic acid derivative - Thioether - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic metalloid moeity - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 382.200 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 6 Exact Mass 382.096 Da Monoisotopic Mass 382.096 Da Topological Polar Surface Area 108.000 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 480.000 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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