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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino 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.
Panoramica Information
7-Methoxyisoflavone 7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK) .
Targets
AMPK
Specifications Sinonimi
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
Specifiche e purezza
10mM in DMSO
Meccanismi biochimici e fisiologici
7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK).
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Proprietà del prodotto ALogP 2.85 hba_count 3 Legame rotabile 2
Nomi e identificatori Pubchem Sid 528762788 Sorrisi canonici 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 Isomeri SMILES COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=CC=C3 Peso molecolare 252.26 Reaxy-Rn 220440 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=220440&ln=
Documentazione 📋 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 Descrizione 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche DMSO (mg/mL) Solubilità massima 30 DMSO (mM) Solubilità massima 118.924918734639 Acqua (mg/mL) Solubilità massima ＜1 Peso molecolare 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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