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· · COA & SDS available for every product · Same-day shipping on in-stock items MT-8 - Moligand™ , Inhibitor of TPC2, CAS No.2284-31-3, Inhibitor of TPC2
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Synonyms
5,7-Dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one | 5,7,3'-trihydroxy-4'-methoxyisoflavone | UNII-D2CF8CJ6AP | HY-N7981 | E88870 | Q3401397 | CHEBI:8359 | SCHEMBL73557 | LMPK12050265 | Pratensein | 5,7-dihydroxy-3-(3-hydroxy-4-methoxypheny
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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
5, 7-Dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one | 5, 7, 3'-trihydroxy-4'-methoxyisoflavone | UNII-D2CF8CJ6AP | HY-N7981 | E88870 | Q3401397 | CHEBI:8359 | SCHEMBL73557 | LMPK12050265 | Pratensein | 5, 7-dihydroxy-3-(3-hydroxy-4-methoxypheny
Specifications & Purity
Moligand™
Mechanism of action
Inhibitor of TPC2
Names and Identifiers Canonical Smiles COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O IUPAC Name 5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one InChIKey FPIOBTBNRZPWJW-UHFFFAOYSA-N INCHI 1S/C16H12O6/c1-21-13-3-2-8(4-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3 Isomeric SMILES COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O Alternate CAS 2284-31-3 PubChem CID 5281803 MeSH Entry Terms 4'-methoxy-3',5,7-trihydroxyisoflavone;4776B compound;pratensein
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 Phenylpropanoids and polyketides Class Isoflavonoids Subclass O-methylated isoflavonoids Intermediate Tree Nodes 4'-O-methylated isoflavonoids Direct Parent 3'-hydroxy,4'-methoxyisoflavonoids Alternative Parents 4'-O-methylisoflavones Hydroxyisoflavonoids Isoflavones Chromones Methoxyphenols Anisoles Phenoxy compounds Methoxybenzenes 1-hydroxy-4-unsubstituted benzenoids Pyranones and derivatives 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Heteroaromatic compounds Vinylogous acids Oxacyclic compounds Hydrocarbon derivatives Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents 3'-hydroxy,4'-methoxyisoflavonoid - 4p-o-methylisoflavone - Isoflavone - Hydroxyisoflavonoid - Chromone - Methoxyphenol - 1-benzopyran - Benzopyran - Phenoxy compound - Phenol ether - Anisole - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Pyranone - Benzenoid - Pyran - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous acid - Ether - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as 3'-hydroxy,4'-methoxyisoflavonoids. These are isoflavonoids carrying a methoxy group attached to the C4' atom, as well as a hydroxyl group at the C3'-position of the isoflavonoid backbone. External Descriptors Isoflavonoids 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 Molecular Weight 300.260 g/mol XLogP3 2.600 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 2 Exact Mass 300.063 Da Monoisotopic Mass 300.063 Da Topological Polar Surface Area 96.200 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 462.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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