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· · COA & SDS available for every product · Same-day shipping on in-stock items Toosendanin - 10mM in DMSO , CAS No.58812-37-6
GRADE & PURITY 10mM in DMSO
Synonyms
12-Acetoxyamoorastatin | AKOS025311566 | MFCD00210564 | CHEBI:192461 | Toosendanin | [(1S,2R,4R,5R,6S,8R,10S,11S,12R,14R,15R,16R,19S,21R)-4-acetyloxy-6-(uran-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08
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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
12-Acetoxyamoorastatin | AKOS025311566 | MFCD00210564 | CHEBI:192461 | Toosendanin | [(1S, 2R, 4R, 5R, 6S, 8R, 10S, 11S, 12R, 14R, 15R, 16R, 19S, 21R)-4-acetyloxy-6-(uran-3-yl)-12, 16, 19-trihydroxy-5, 11, 15-trimethyl-3-oxo-9, 17-dioxahexacyclo[13.3.3.01, 14.02, 11.05, 10.08
Specifications & Purity
10mM in DMSO
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)OC1CC(C23COC(C1(C2CC(C4(C3C(=O)C(C5(C46C(O6)CC5C7=COC=C7)C)OC(=O)C)C)O)C)O)O IUPAC Name [(1S,2R,4R,5R,6S,8R,10S,11S,12R,14R,15R,16R,19S,21R)-4-acetyloxy-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.01,14.02,11.05,10.08,10]henicosan-21-yl] acetate InChIKey NAHTXVIXCMUDLF-RFNFAWMESA-N INCHI 1S/C30H38O11/c1-13(31)39-20-10-19(34)29-12-38-25(36)26(20,3)17(29)9-18(33)28(5)23(29)22(35)24(40-14(2)32)27(4)16(15-6-7-37-11-15)8-21-30(27,28)41-21/h6-7,11,16-21,23-25,33-34,36H,8-10,12H2,1-5H3/t16-,17-,18+,19-,20+,21+,23-,24-,25+,26+,27+,28+,29+,30+/m0/s1 Isomeric SMILES CC(=O)O[C@@H]1C[C@@H]([C@@]23CO[C@H]([C@@]1([C@@H]2C[C@H]([C@@]4([C@@H]3C(=O)[C@@H]([C@@]5([C@]46[C@H](O6)C[C@H]5C7=COC=C7)C)OC(=O)C)C)O)C)O)O PubChem CID 9851101 Molecular Weight 574.62
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 Triterpenoids Intermediate Tree Nodes Not available Direct Parent Limonoids Alternative Parents 17-furanylsteroids and derivatives Steroid esters Naphthopyrans Naphthalenes Alpha-acyloxy ketones Pyrans Oxanes Dicarboxylic acids and derivatives Heteroaromatic compounds Furans Secondary alcohols Carboxylic acid esters Ketones Cyclic alcohols and derivatives Hemiacetals Polyols Oxacyclic compounds Epoxides Dialkyl ethers Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Limonoid skeleton - 17-furanylsteroid skeleton - Steroid ester - Naphthopyran - Naphthalene - Alpha-acyloxy ketone - Dicarboxylic acid or derivatives - Oxane - Pyran - Cyclic alcohol - Furan - Heteroaromatic compound - Secondary alcohol - Carboxylic acid ester - Hemiacetal - Ketone - Polyol - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Organoheterocyclic compound - Oxirane - Ether - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. 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(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Melt Point(°C) 244-245°C Molecular Weight 574.600 g/mol XLogP3 0.700 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 11 Rotatable Bond Count 5 Exact Mass 574.241 Da Monoisotopic Mass 574.241 Da Topological Polar Surface Area 165.000 Ų Heavy Atom Count 41 Formal Charge 0 Complexity 1190.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 14 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 References 1. Benshui Shu, Yanzheng Lin, Yuting Huang, Luyang Liu, Xueming Cai, Jintian Lin, Jingjing Zhang. (2023) Characterization and transcriptomic analyses of the toxicity induced by toosendanin in Spodoptera frugipreda. GENE, [PMID:37898452 ] [10.1016/j.gene.2023.147928 ] 2. Zhiping Che, Xiaolong Guo, Yuanhao Li, Song Zhang, Lina Zhu, Jiaxuan He, Di Sun, Yihao Guo, Yibo Liu, Ruxue Wei, Xiaobo Huang, Shengming Liu, Genqiang Chen, Yuee Tian. (2022) Synthesis of paeonol ester derivatives and their insecticidal, nematicidal, and anti-oomycete activities. PEST MANAGEMENT SCIENCE, 78 (8): (3442-3455). [PMID:35567371 ] [10.1002/ps.6985 ] 3. Shaobin Xu, Jiaxuan He, Genqiang Chen, Xiaobo Huang, Yuee Tian, Zhiping Che. (2025) Design, Synthesis, Anti-Oomycete, and Insecticidal Activities of 3β-Acyloxy-18β-Glycyrrhetinic Acid Derivatives. CHEMISTRY & BIODIVERSITY, [PMID:41135017 ] [10.1002/cbdv.202502978 ]
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