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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager 7-Methoxyisoflavone - 10mM in DMSO , CAS No.1621-56-3
GRADE & PURITY 10mM in DMSO
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
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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht Information
7-Methoxyisoflavone 7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK) .
Targets
AMPK
Specifications Synonyme
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
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK).
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Produkteigenschaften ALogP 2.85 hba_count 3 Rotationsfähige Bindung 2
Namen und Kennungen Pubchem Sid 528762788 Kanonisches Lächeln 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 Isomere SMILES COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=CC=C3 Molekulargewicht 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 Klasse 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 Beschreibung 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften DMSO (mg/ml) Maximale Löslichkeit 30 DMSO (mM) Maximale Löslichkeit 118.924918734639 Wasser (mg/ml) Maximale Löslichkeit ＜1 Molekulargewicht 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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