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· · COA & SDS available for every product · 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.
Overview Pseudolaric acid A-O-β-D-glucopyranoside, isolated from Cortex Pseudolaricis, demonstrates antifungal and antifertility activities.
Form:Solid
Specifications 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
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
Pseudolaric acid A-O-β-D-glucopyranoside, isolated from Cortex Pseudolaricis, demonstrates antifungal and antifertility activities.
Storage
Store at 2-8°C, Protected from light, Desiccated
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles 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 Isomeric 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 Alternate CAS 98891-44-2 PubChem CID 44566375 Molecular Weight 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 Class 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 Description 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.
3D Structure Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 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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