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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock BMS-986318 - Moligand™ , Agonist of Farnesoid X receptor, CAS No.B608161, Agonist of Farnesoid X receptor
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
2314378-09-9 | YO3W29IM33 | UNII-YO3W29IM33 | SCHEMBL20952191 | EX-A6049 | HY-139562 | compound 1 [PMID: 34531950] | BDBM50572221 | GTPL11728 | WPGAVSDZYIRUGE-UHFFFAOYSA-N | BMS986318 | BMS-986318 | 2-Quinolinecarboxylic acid, 6-(2-(5-cyclopropyl-3-(3,5-d
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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
2314378-09-9 | YO3W29IM33 | UNII-YO3W29IM33 | SCHEMBL20952191 | EX-A6049 | HY-139562 | compound 1 [PMID: 34531950] | BDBM50572221 | GTPL11728 | WPGAVSDZYIRUGE-UHFFFAOYSA-N | BMS986318 | BMS-986318 | 2-Quinolinecarboxylic acid, 6-(2-(5-cyclopropyl-3-(3,5-d
Spécifications et pureté
Moligand™
Conditions de stockage de stockage
Room temperature
Mécanisme d'action
Agonist of Farnesoid X receptor
Noms et identifiants Sourires canoniques C1(CC1)c1c(c(no1)c1c(cncc1Cl)Cl)C1=CC2(C1)CCN(CC2)c1cc2c(cc(nc2cc1)C(=O)O)C(F)(F)F InChIKey WPGAVSDZYIRUGE-UHFFFAOYSA-N INCHI 1S/C30H23Cl2F3N4O3/c31-20-13-36-14-21(32)25(20)26-24(27(42-38-26)15-1-2-15)16-11-29(12-16)5-7-39(8-6-29)17-3-4-22-18(9-17)19(30(33,34)35)10-23(37-22)28(40)41/h3-4,9-11,13-15H,1-2,5-8,12H2,(H,40,41) Isomères SMILES C1CC1C2=C(C(=NO2)C3=C(C=NC=C3Cl)Cl)C4=CC5(C4)CCN(CC5)C6=CC7=C(C=C6)N=C(C=C7C(F)(F)F)C(=O)O PubChem CID 138592025
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 Quinoline carboxylic acids Intermediate Tree Nodes Not available Direct Parent Quinoline carboxylic acids Alternative Parents Aminoquinolines and derivatives Pyridinecarboxylic acids Polyhalopyridines Dialkylarylamines 5-cyclopropylisoxazoles Hydroxypyridines Heterocyclic fatty acids Halogenated fatty acids Branched fatty acids 2-halopyridines Piperidines Benzenoids Secondary ketimines Heteroaromatic compounds Trialkylamines Amino acids Vinyl chlorides Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Enamines Chloroalkenes Carboxylic acids Azacyclic compounds Aldimines Organopnictogen compounds Organooxygen compounds Organofluorides Organochlorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Molecular Framework Aromatic heteropolycyclic compounds Substituents Quinoline-2-carboxylic acid - Aminoquinoline - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - 5-cyclopropylisoxazole - Cyclopropylisoxazole - Polyhalopyridine - Dialkylarylamine - Tertiary aliphatic/aromatic amine - 2-halopyridine - Hydroxypyridine - Heterocyclic fatty acid - Halogenated fatty acid - Branched fatty acid - Fatty acyl - Benzenoid - Pyridine - Piperidine - Heteroaromatic compound - Secondary ketimine - Isoxazole - Azole - Amino acid - Tertiary aliphatic amine - Tertiary amine - Ketimine - Amino acid or derivatives - Oxacycle - Azacycle - Chloroalkene - Haloalkene - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Vinyl halide - Vinyl chloride - Monocarboxylic acid or derivatives - Enamine - Carboxylic acid - Carboxylic acid derivative - Aldimine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organochloride - Organohalogen compound - Imine - Amine - Alkyl halide - Alkyl fluoride - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions. 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) Calculateurs de solution 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 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 →
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