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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Salicylidene salicylhydrazide (SCS) - Moligand™, ≥97% , CAS No.3232-36-8
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. ≥97% Synonyms
N-Salicylidene-N'-salicyloylhydrazine | N-Salicylidene-N-salicyloylhydrazine | SR-01000872611-3 | SALICYLIDENESALICYLHYDRAZIDE | 2-Hydroxy-N'-[(E)-(2-hydroxyphenyl)methylidene]benzohydrazide | 2-HYDROXY-N'~1~-[(2-HYDROXYPHENYL)METHYLENE]BENZOHYDRAZIDE | S
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Why this grade Moligand™, ≥97% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
N-Salicylidene-N'-salicyloylhydrazine | N-Salicylidene-N-salicyloylhydrazine | SR-01000872611-3 | SALICYLIDENESALICYLHYDRAZIDE | 2-Hydroxy-N'-[(E)-(2-hydroxyphenyl)methylidene]benzohydrazide | 2-HYDROXY-N'~1~-[(2-HYDROXYPHENYL)METHYLENE]BENZOHYDRAZIDE | S
Especificaciones y pureza
Moligand™, ≥97%
Mecanismos bioquímicos y fisiológicos
Potent and selective partial inhibitor ofβ1-containing GABAAreceptors (IC50values are 4.5, 5.3 and 7.9 nM atα2β1γ1θ, α2β1γ1 andα2β1γ2s GABAAreceptors respectively). May bind allosterically to a novel site on GABAAreceptor.
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 504773333 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504773333 Sonrisas canónicas C1=CC=C(C(=C1)C=NNC(=O)C2=CC=CC=C2O)O IUPAC Name 2-hydroxy-N-[(E)-(2-hydroxyphenyl)methylideneamino]benzamide InChIKey OMCYEZUIYGPHDJ-OQLLNIDSSA-N INCHI 1S/C14H12N2O3/c17-12-7-3-1-5-10(12)9-15-16-14(19)11-6-2-4-8-13(11)18/h1-9,17-18H,(H,16,19)/b15-9+ Isómeros SMILES C1=CC=C(C(=C1)/C=N/NC(=O)C2=CC=CC=C2O)O PubChem CID 135445765 Peso molecular 256.26
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 Clase Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Hydroxybenzoic acid derivatives - Salicylic acid and derivatives Direct Parent Salicylamides Alternative Parents Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Carboxylic acids and derivatives Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Salicylamide - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as salicylamides. These are carboxamide derivatives of salicylic acid. Salicylic acid is the ortho-hydroxylated derivative of benzoic acid. 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 (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:DMSO, Max Conc. mg/mL: 12.81, Max Conc. mM: 50 Peso molecular 256.260 g/mol XLogP3 2.700 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 256.085 Da Monoisotopic Mass 256.085 Da Topological Polar Surface Area 81.900 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 333.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
Citations of This Product Referencias 1. Cheng Li, Yang Tian, Jiahuan Pei, Yuyang Zhang, Daokuan Hao, Tianjiao Han, Xiaoqin Wang, Shuang Song, Linjuan Huang, Zhongfu Wang. (2023) Sea cucumber chondroitin sulfate polysaccharides attenuate OVA-induced food allergy in BALB/c mice associated with gut microbiota metabolism and Treg cell differentiation. Food & Function, 14 (16): (7375-7386). [PMID:37477050 ] [10.1039/D3FO00146F ]
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