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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock 7-Methoxyisoflavone - ≥98% , CAS No.1621-56-3
Synonyms
MS-23560 | MLS001049012 | HY-N6631 | Cambridge id 5141113 | 7-methoxy-3-phenyl-4H-chromen-4-one | HMS1413J15 | IECSQLKWZBEUGA-UHFFFAOYSA-N | MFCD00181416 | SMR000387026 | EU-0036440 | DTXSID00348530 | NCGC00142583-01 | AKOS002183364 | CCG-47937 | AB001291
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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.
Vue d’ensemble Information
7-Methoxyisoflavone 7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK) .
Targets
AMPK
Specifications Synonymes
MS-23560 | MLS001049012 | HY-N6631 | Cambridge id 5141113 | 7-methoxy-3-phenyl-4H-chromen-4-one | HMS1413J15 | IECSQLKWZBEUGA-UHFFFAOYSA-N | MFCD00181416 | SMR000387026 | EU-0036440 | DTXSID00348530 | NCGC00142583-01 | AKOS002183364 | CCG-47937 | AB001291
Spécifications et pureté
≥98%
Mécanismes biochimiques et physiologiques
7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK).
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Propriétés du produit ALogP 2.85 hba_count 3 Liaison rotative 2
Noms et identifiants Pubchem Sid 488190867 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488190867 Sourires canoniques COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=CC=C3 IUPAC Name 7-methoxy-3-phenylchromen-4-one InChIKey IECSQLKWZBEUGA-UHFFFAOYSA-N INCHI 1S/C16H12O3/c1-18-12-7-8-13-15(9-12)19-10-14(16(13)17)11-5-3-2-4-6-11/h2-10H,1H3 Isomères SMILES COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=CC=C3 Poids moléculaire 252.26 Reaxy-Rn 220440 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=220440&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 Phenylpropanoids and polyketides Classe Isoflavonoids Subclass O-methylated isoflavonoids Intermediate Tree Nodes 7-O-methylated isoflavonoids Direct Parent 7-O-methylisoflavones Alternative Parents Isoflavones Chromones Anisoles Pyranones and derivatives Alkyl aryl ethers Benzene and substituted derivatives Heteroaromatic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 7-o-methylisoflavone - Isoflavone - Chromone - Benzopyran - 1-benzopyran - Anisole - Alkyl aryl ether - Pyranone - Pyran - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Oxacycle - Ether - Organoheterocyclic compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone. External Descriptors methoxyisoflavone 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Solubility (25°C) In vitro DMSO: 30 mg/mL (118.92 mM); Water: Insoluble; Ethanol: Insoluble; DMSO (mg/mL) Solubilité maximale 30 DMSO (mM) Solubilité maximale 118.924918734639 Eau (mg/mL) Solubilité maximale ＜1 Poids moléculaire 252.260 g/mol XLogP3 3.200 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 2 Exact Mass 252.079 Da Monoisotopic Mass 252.079 Da Topological Polar Surface Area 35.500 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 368.000 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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