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· · COA & SDS available for every product · Same-day shipping on in-stock items Asperuloside - 10mM in DMSO , CAS No.14259-45-1
GRADE & PURITY 10mM in DMSO
Synonyms
UNII-V3CFI02X39 | IBIPGYWNOBGEMH-DILZHRMZSA-N | MFCD00673989 | EINECS 238-137-5 | NCGC00380739-01 | (2AS,4AS,5S,7BS)-4-((ACETYLOXY)METHYL)-5-(beta-D-GLUCOPYRANOSYLOXY)-2A,4A,5,7B-TETRAHYDRO-1H-2,6-DIOXACYCLOPENT(CD)INDEN-1-ONE | DTXSID70878339 | [(2aS,4aS
Storage
Protected from light,Store at -80°C
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 Protected from light,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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
UNII-V3CFI02X39 | IBIPGYWNOBGEMH-DILZHRMZSA-N | MFCD00673989 | EINECS 238-137-5 | NCGC00380739-01 | (2AS, 4AS, 5S, 7BS)-4-((ACETYLOXY)METHYL)-5-(beta-D-GLUCOPYRANOSYLOXY)-2A, 4A, 5, 7B-TETRAHYDRO-1H-2, 6-DIOXACYCLOPENT(CD)INDEN-1-ONE | DTXSID70878339 | [(2aS, 4aS
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Asperuloside has shown potential anti-obesity properties through its suppression of increased white adipose tissue, plasma triglycerides, and free fatty acids in the metabolic syndrome-like mouse model.
Storage
Protected from light, Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O IUPAC Name [(4S,7S,8S,11S)-2-oxo-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-6-yl]methyl acetate InChIKey IBIPGYWNOBGEMH-DILZHRMZSA-N INCHI 1S/C18H22O11/c1-6(20)25-4-7-2-9-12-8(16(24)27-9)5-26-17(11(7)12)29-18-15(23)14(22)13(21)10(3-19)28-18/h2,5,9-15,17-19,21-23H,3-4H2,1H3/t9-,10+,11+,12-,13+,14-,15+,17-,18-/m0/s1 Isomeric SMILES CC(=O)OCC1=C[C@H]2[C@H]3[C@@H]1[C@@H](OC=C3C(=O)O2)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O Molecular Weight 414.4 Reaxy-Rn 54967385 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=54967385&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 Organic oxygen compounds Class Organooxygen compounds Subclass Carbohydrates and carbohydrate conjugates Intermediate Tree Nodes Glycosyl compounds Direct Parent O-glycosyl compounds Alternative Parents Hexoses Furopyrans Pyrans Oxanes Dicarboxylic acids and derivatives Gamma butyrolactones Vinylogous esters Tetrahydrofurans Enoate esters Furans Secondary alcohols Acetals Polyols Oxacyclic compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Primary alcohols Molecular Framework Aliphatic heteropolycyclic compounds Substituents Hexose monosaccharide - O-glycosyl compound - Furopyran - Dicarboxylic acid or derivatives - Gamma butyrolactone - Monosaccharide - Oxane - Pyran - Vinylogous ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tetrahydrofuran - Furan - Secondary alcohol - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Carboxylic acid derivative - Polyol - Oxacycle - Acetal - Primary alcohol - Carbonyl group - Organic oxide - Alcohol - Hydrocarbon derivative - Aliphatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. External Descriptors Iridoids 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(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Light sensitive Molecular Weight 414.400 g/mol XLogP3 -2.400 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 11 Rotatable Bond Count 6 Exact Mass 414.116 Da Monoisotopic Mass 414.116 Da Topological Polar Surface Area 161.000 Ų Heavy Atom Count 29 Formal Charge 0 Complexity 746.000 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
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