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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Recibufogenin - ≥98% , CAS No.465-39-4
Synonyms
Q63391924 | 5-[(1R,2S,4R,6R,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one | DTXCID8026808 | s3238 | CAS-465-39-4 | CHEBI:31319 | Respigon | Bufogenine [INN-French] | 3beta-hydroxy-5beta,15be
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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.
Descripción general product description：
Resibufogenin is isolated from the skin venom of the Asiatic toad (Bufo gargarizans) known as Chan su in Traditional Chinese Medicine.
Specifications Sinónimos
Q63391924 | 5-[(1R, 2S, 4R, 6R, 7R, 10S, 11S, 14S, 16R)-14-hydroxy-7, 11-dimethyl-3-oxapentacyclo[8.8.0.02, 4.02, 7.011, 16]octadecan-6-yl]pyran-2-one | DTXCID8026808 | s3238 | CAS-465-39-4 | CHEBI:31319 | Respigon | Bufogenine [INN-French] | 3beta-hydroxy-5beta, 15be
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Resibufogenin, a component of huachansu, has been shown to exhibit the anti-proliferative effect against cancer cells, and this may be attributed to the degradation of cyclin D1 caused by the activation of GSK-3β. IC50 Value: Target: In vitro: The effects
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)O IUPAC Name 5-[(1R,2S,4R,6R,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one InChIKey ATLJNLYIJOCWJE-CWMZOUAVSA-N INCHI 1S/C24H32O4/c1-22-9-7-16(25)11-15(22)4-5-18-17(22)8-10-23(2)19(12-20-24(18,23)28-20)14-3-6-21(26)27-13-14/h3,6,13,15-20,25H,4-5,7-12H2,1-2H3/t15-,16+,17+,18-,19-,20-,22+,23-,24-/m1/s1 Isómeros SMILES C[C@]12CC[C@@H](C[C@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@]35[C@H](O5)C[C@@H]4C6=COC(=O)C=C6)C)O PubChem CID 6917974 Peso molecular 384.51
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 Lipids and lipid-like molecules Clase Steroids and steroid derivatives Subclass Steroid lactones Intermediate Tree Nodes Not available Direct Parent Bufanolides and derivatives Alternative Parents Naphthopyrans Naphthalenes Pyranones and derivatives Oxanes Heteroaromatic compounds Secondary alcohols Lactones Cyclic alcohols and derivatives Oxacyclic compounds Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Bufanolide-skeleton - Naphthopyran - Naphthalene - Pyranone - Pyran - Oxane - Cyclic alcohol - Heteroaromatic compound - Lactone - Secondary alcohol - Dialkyl ether - Oxirane - Ether - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organooxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative. 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 Sensibilidad Air sensitive Peso molecular 384.500 g/mol XLogP3 3.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 384.23 Da Monoisotopic Mass 384.23 Da Topological Polar Surface Area 59.100 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 785.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 9 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
Citations of This Product Referencias 1. Min Wang, Yin Zhao, Shuai Yuan, Zhuyi Wang, Xin Ren, Meihong Zhang, Liyi Shi, Dongdong Li. (2014) High electro-catalytic counter electrode based on three-dimensional conductive grid for dye-sensitized solar cell. CHEMICAL ENGINEERING JOURNAL, [PMID: [10.1016/j.cej.2014.06.043 ]
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