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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Tubacina - ≥96%(HPLC) , CAS No.1350555-93-9
Synonyms
02C2G1D30D | N1-(4-((2R,4R,6S)-4-((4,5-diphenyloxazol-2-ylthio)methyl)-6-(4-(hydroxymethyl)phenyl)-1,3-dioxan-2-yl)phenyl)-N8-hydroxyoctanediamide | Tubacin, >=98% (HPLC) | UNII-02C2G1D30D | HB1403 | Tubacin | N1-[4-[(2R,4R,6S)-4-[[(4,5-diphenyl-2-oxazoly
Shipped In
Hielera + almohadillas de hielo
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Why this grade ≥96%(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
02C2G1D30D | N1-(4-((2R, 4R, 6S)-4-((4, 5-diphenyloxazol-2-ylthio)methyl)-6-(4-(hydroxymethyl)phenyl)-1, 3-dioxan-2-yl)phenyl)-N8-hydroxyoctanediamide | Tubacin, >=98% (HPLC) | UNII-02C2G1D30D | HB1403 | Tubacin | N1-[4-[(2R, 4R, 6S)-4-[[(4, 5-diphenyl-2-oxazoly
Especificaciones y pureza
≥96%(HPLC)
Mecanismos bioquímicos y fisiológicos
Inhibidor selectivo de HDAC6; inhibe el segundo dominio desacetilasa (DD2). No inhibe la actividad de la histona desacetilasa HDAC6; inhibe reversiblemente la desacetilación de al-tubulina. Aumenta los niveles de acetilación de al-tubulina sin afectar a l
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Nombres e identificadores Sonrisas canónicas C1C(OC(OC1C2=CC=C(C=C2)CO)C3=CC=C(C=C3)NC(=O)CCCCCCC(=O)NO)CSC4=NC(=C(O4)C5=CC=CC=C5)C6=CC=CC=C6 IUPAC Name N-[4-[(2R,4R,6S)-4-[(4,5-diphenyl-1,3-oxazol-2-yl)sulfanylmethyl]-6-[4-(hydroxymethyl)phenyl]-1,3-dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide InChIKey BHUZLJOUHMBZQY-YXQOSMAKSA-N INCHI 1S/C41H43N3O7S/c45-26-28-17-19-29(20-18-28)35-25-34(27-52-41-43-38(30-11-5-3-6-12-30)39(51-41)31-13-7-4-8-14-31)49-40(50-35)32-21-23-33(24-22-32)42-36(46)15-9-1-2-10-16-37(47)44-48/h3-8,11-14,17-24,34-35,40,45,48H,1-2,9-10,15-16,25-27H2,(H,42,46)(H,44,47)/t34-,35+,40+/m1/s1 Isómeros SMILES C1[C@@H](O[C@@H](O[C@@H]1C2=CC=C(C=C2)CO)C3=CC=C(C=C3)NC(=O)CCCCCCC(=O)NO)CSC4=NC(=C(O4)C5=CC=CC=C5)C6=CC=CC=C6 PubChem CID 6675804 Peso molecular 721.86
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 Azoles Subclass Oxazoles Intermediate Tree Nodes Not available Direct Parent Phenyl-1,3-oxazoles Alternative Parents Anilides 2,4,5-trisubstituted oxazoles N-arylamides Benzyl alcohols Alkylarylthioethers 1,3-dioxanes Fatty amides Heteroaromatic compounds Secondary carboxylic acid amides Hydroxamic acids Sulfenyl compounds Oxacyclic compounds Acetals Azacyclic compounds Aromatic alcohols Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds Primary alcohols Molecular Framework Aromatic heteromonocyclic compounds Substituents Phenyl-1,3-oxazole - Anilide - Aryl thioether - 2,4,5-trisubstituted 1,3-oxazole - Benzyl alcohol - N-arylamide - Alkylarylthioether - Meta-dioxane - Monocyclic benzene moiety - Fatty amide - Fatty acyl - Benzenoid - Heteroaromatic compound - Carboxamide group - Hydroxamic acid - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Sulfenyl compound - Thioether - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organooxygen compound - Organosulfur compound - Primary alcohol - Organopnictogen compound - Aromatic alcohol - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as phenyl-1,3-oxazoles. These are aromatic heterocyclic compounds containing a 1,3-oxazole substituted at one or more positions by a phenyl 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.
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: 7.22, Max Conc. mM: 10 Peso molecular 721.900 g/mol XLogP3 6.300 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 16 Exact Mass 721.282 Da Monoisotopic Mass 721.282 Da Topological Polar Surface Area 168.000 Ų Heavy Atom Count 52 Formal Charge 0 Complexity 1060.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 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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