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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items FX 1 - ≥98%(HPLC) , CAS No.1426138-42-2
Synonyms
ácido (5Z)-5-(5-cloro-1,2-dihidro-2-oxo-3H-indol-3-ilideno)-4-oxo-2-tioxo-3-tiazolidinopropanoico | FX1 | (Z)-3-(5-(5-cloro-2-oxoindolin-3-ilideno)-4-oxo-2-tioxotiazolidin-3-il)propanoico, (5Z)-5-(5-Chloro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)-4-o
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
ácido (5Z)-5-(5-cloro-1, 2-dihidro-2-oxo-3H-indol-3-ilideno)-4-oxo-2-tioxo-3-tiazolidinopropanoico | FX1 | (Z)-3-(5-(5-cloro-2-oxoindolin-3-ilideno)-4-oxo-2-tioxotiazolidin-3-il)propanoico, (5Z)-5-(5-Chloro-1, 2-dihydro-2-oxo-3H-indol-3-ylidene)-4-o
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Inhibidor de Bcl-6 (Kd= 3 μM); presenta una potencia 10 veces mayor que los corepresores de Bcl-6 endógenos. Interrumpe la formación del complejo de represión de Bcl-6. Induce la regresión de tumores establecidos en ratones portadores de xenoinjertos de L
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Nombres e identificadores Pubchem Sid 504773449 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504773449 Sonrisas canónicas C1=CC2=NC(=O)C(=C2C=C1Cl)C3=C(N(C(=S)S3)CCC(=O)O)O IUPAC Name 3-[5-(5-chloro-2-oxoindol-3-yl)-4-hydroxy-2-sulfanylidene-1,3-thiazol-3-yl]propanoic acid InChIKey JYBGCTWNOMSQJY-UHFFFAOYSA-N INCHI 1S/C14H9ClN2O4S2/c15-6-1-2-8-7(5-6)10(12(20)16-8)11-13(21)17(14(22)23-11)4-3-9(18)19/h1-2,5,21H,3-4H2,(H,18,19) Isómeros SMILES C1=CC2=NC(=O)C(=C2C=C1Cl)C3=C(N(C(=S)S3)CCC(=O)O)O PubChem CID 135886621 Peso molecular 368.82
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 Clase Indoles and derivatives Subclass Not available Intermediate Tree Nodes Not available Direct Parent Indoles and derivatives Alternative Parents Benzenoids Aryl chlorides Thiazoles Heteroaromatic compounds N-acylimines Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organosulfur compounds Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Indole or derivatives - Benzenoid - Aryl halide - Aryl chloride - Heteroaromatic compound - Thiazole - Azole - N-acylimine - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Carbonyl group - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 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) 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: 36.88, Max Conc. mM: 100 Peso molecular 368.800 g/mol XLogP3 1.400 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 4 Exact Mass 367.969 Da Monoisotopic Mass 367.969 Da Topological Polar Surface Area 148.000 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 808.000 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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