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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Pseudolaric acid A-O-β-D-glucopyranoside - ≥99% , CAS No.98891-44-2
Synonyms
PD196254 | E88597 | A-D-glucopyranoside | Pseudolaric Acid A-O-beta-D-glucopyranoside | DTXSID001276462 | MS-30074 | Pseudolaric acid A-O- | HY-N4088 | PseudolaricacidAbeta-D-glucoside | AC-34823 | pseudolaric acid A O-beta-d-glucopyranoside | AKOS037514
Storage
Store at 2-8°C,Protected from light,Desiccated
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Why this grade ≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Desiccated Ships Wet ice 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.
Descripción general Pseudolaric acid A-O-β-D-glucopyranoside, isolated from Cortex Pseudolaricis, demonstrates antifungal and antifertility activities.
Form:Solid
Specifications Sinónimos
PD196254 | E88597 | A-D-glucopyranoside | Pseudolaric Acid A-O-beta-D-glucopyranoside | DTXSID001276462 | MS-30074 | Pseudolaric acid A-O- | HY-N4088 | PseudolaricacidAbeta-D-glucoside | AC-34823 | pseudolaric acid A O-beta-d-glucopyranoside | AKOS037514
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
Pseudolaric acid A-O-β-D-glucopyranoside, isolated from Cortex Pseudolaricis, demonstrates antifungal and antifertility activities.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Desiccated
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O IUPAC Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2E,4E)-5-[(1R,7S,8S,9R)-7-acetyloxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoate InChIKey IVYWRYGMQNKDQB-VHJBJYHKSA-N INCHI 1S/C28H38O11/c1-15-7-11-27-12-9-19(28(27,13-8-15)38-17(3)30)26(4,39-25(27)35)10-5-6-16(2)23(34)37-24-22(33)21(32)20(31)18(14-29)36-24/h5-7,10,18-22,24,29,31-33H,8-9,11-14H2,1-4H3/b10-5+,16-6+/t18-,19+,20-,21+,22-,24+,26-,27-,28+/m1/s1 Isómeros SMILES CC1=CC[C@]23CC[C@H]([C@]2(CC1)OC(=O)C)[C@@](OC3=O)(C)/C=C/C=C(\C)/C(=O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O CAS alternativo 98891-44-2 PubChem CID 44566375 Peso molecular 550.59
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 Prenol lipids Subclass Terpene lactones Intermediate Tree Nodes Not available Direct Parent Diterpene lactones Alternative Parents Sphenolobane diterpenoids Hexoses Tricarboxylic acids and derivatives Delta valerolactones Oxepanes Fatty acid esters Oxanes Enoate esters Secondary alcohols Acetals Polyols Oxacyclic compounds Carbonyl compounds Primary alcohols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic heteropolycyclic compounds Substituents Diterpene lactone - Diterpenoid - Prenyldaucane diterpenoid - Hexose monosaccharide - Tricarboxylic acid or derivatives - Caprolactone - Delta valerolactone - Fatty acid ester - Delta_valerolactone - Oxepane - Oxane - Monosaccharide - Fatty acyl - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Secondary alcohol - Lactone - Carboxylic acid ester - Polyol - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Acetal - Primary alcohol - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - Organooxygen compound - Organic oxygen compound - Aliphatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 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 Peso molecular 550.600 g/mol XLogP3 0.900 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 11 Rotatable Bond Count 8 Exact Mass 550.241 Da Monoisotopic Mass 550.241 Da Topological Polar Surface Area 169.000 Ų Heavy Atom Count 39 Formal Charge 0 Complexity 1100.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 9 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 2 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 2 Covalently-Bonded Unit Count 1
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