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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Oroxylin A - 10mM in DMSO , CAS No.480-11-5
GRADE & PURITY 10mM in DMSO
Synonyms
53K24Z586G | Oroxylin-A | BCP31803 | HY-N0560 | LMPK12111096 | BDBM50430091 | SGCUT00130 | FLAVONE, 5,7-DIHYDROXY-6-METHOXY- | UNII-53K24Z586G | EX-A4028 | O-160 | s9204 | AC-31960 | Oroxylia A | 1,4-Diaminobutane, N,N'-bis(3-aminopropyl)- | CHEBI:61668 |
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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
53K24Z586G | Oroxylin-A | BCP31803 | HY-N0560 | LMPK12111096 | BDBM50430091 | SGCUT00130 | FLAVONE, 5, 7-DIHYDROXY-6-METHOXY- | UNII-53K24Z586G | EX-A4028 | O-160 | s9204 | AC-31960 | Oroxylia A | 1, 4-Diaminobutane, N, N'-bis(3-aminopropyl)- | CHEBI:61668 |
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Oroxylin A is a flavonoid isolated from Scutellaria baicalensis, which is one of the most important medicinal herbs in traditional Korean/Chinese/Japanese medicine. The amelioration of Abeta(25-35) peptide-induced memory impairment by oroxylin A is believ
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
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Nombres e identificadores Sonrisas canónicas COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O IUPAC Name 5,7-dihydroxy-6-methoxy-2-phenylchromen-4-one InChIKey LKOJGSWUMISDOF-UHFFFAOYSA-N INCHI 1S/C16H12O5/c1-20-16-11(18)8-13-14(15(16)19)10(17)7-12(21-13)9-5-3-2-4-6-9/h2-8,18-19H,1H3 Isómeros SMILES COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O WGK Alemania 3 Peso molecular 284.26 Reaxy-Rn 281274 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=281274&ln=
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 Phenylpropanoids and polyketides Clase Flavonoids Subclass O-methylated flavonoids Intermediate Tree Nodes Not available Direct Parent 6-O-methylated flavonoids Alternative Parents Flavones 7-hydroxyflavonoids 5-hydroxyflavonoids Chromones Anisoles Pyranones and derivatives Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Vinylogous acids Heteroaromatic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 6-methoxyflavonoid-skeleton - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Chromone - Benzopyran - 1-benzopyran - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Monocyclic benzene moiety - Benzenoid - Pyran - Vinylogous acid - Heteroaromatic compound - Ether - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as 6-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. External Descriptors a flavone 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 Peso molecular 284.260 g/mol XLogP3 2.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 2 Exact Mass 284.068 Da Monoisotopic Mass 284.068 Da Topological Polar Surface Area 76.000 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 426.000 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
Preguntas frecuentes y artículos Citations of This Product Referencias 1. Fuyun Chi, Wenshuang Wang, Shanshan Zhai, Man Zhang, Yuanyuan Hou, Gang Bai. (2025) Self-assembled baicalein-2,4-decadienal nanomedicine synergistically inhibits PGE2 expression and elicits anti-inflammatory responses. Chinese Herbal Medicines, [PMID: [10.1016/j.chmed.2025.10.001 ]
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