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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock D-64131 - ≥97% , CAS No.74588-78-6
Synonyms
CHEBI:92475 | FT-0700358 | (5-Methoxy-1H-indol-2-yl)-phenyl-methanone | ZCA58878 | (5-Methoxy-1H-indol-2-yl)(phenyl)methanone | SR-01000597597-1 | DTXSID30397970 | ICMIJSRDISNKOC-UHFFFAOYSA-N | Tocris-1643 | HMS3676P03 | EC-000.2395 | SCHEMBL5828518 | 5-m
Shipped In
Ice chest + Ice pads
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Why this grade ≥97% 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.
Specifications Synonymes
CHEBI:92475 | FT-0700358 | (5-Methoxy-1H-indol-2-yl)-phenyl-methanone | ZCA58878 | (5-Methoxy-1H-indol-2-yl)(phenyl)methanone | SR-01000597597-1 | DTXSID30397970 | ICMIJSRDISNKOC-UHFFFAOYSA-N | Tocris-1643 | HMS3676P03 | EC-000.2395 | SCHEMBL5828518 | 5-m
Spécifications et pureté
≥97%
Mécanismes biochimiques et physiologiques
Novel inhibitor of tubulin polymerization; cytotoxic and inhibits tumor cell proliferationin vitro(IC50= 74 nM). Prevents growth of tumor models in mice following oral administrationin vivo.
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.
Noms et identifiants Pubchem Sid 504762793 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762793 Sourires canoniques COC1=CC2=C(C=C1)NC(=C2)C(=O)C3=CC=CC=C3 IUPAC Name (5-methoxy-1H-indol-2-yl)-phenylmethanone InChIKey ICMIJSRDISNKOC-UHFFFAOYSA-N INCHI 1S/C16H13NO2/c1-19-13-7-8-14-12(9-13)10-15(17-14)16(18)11-5-3-2-4-6-11/h2-10,17H,1H3 Isomères SMILES COC1=CC2=C(C=C1)NC(=C2)C(=O)C3=CC=CC=C3 Poids moléculaire 251.28 Reaxy-Rn 4464016 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4464016&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 Organoheterocyclic compounds Classe Indoles and derivatives Subclass Benzoylindoles Intermediate Tree Nodes Not available Direct Parent Benzoylindoles Alternative Parents Aryl-phenylketones Indolecarboxylic acids and derivatives Indoles Benzoyl derivatives Anisoles Alkyl aryl ethers Substituted pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Benzoylindole - Aryl-phenylketone - Indolecarboxylic acid derivative - Indole - Anisole - Benzoyl - Aryl ketone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Ketone - Ether - Azacycle - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as benzoylindoles. These are organic compounds containing an indole attached to a benzoyl moiety through the acyl group. 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.
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 Solvent:ethanol, Max Conc. mg/mL: 5.03, Max Conc. mM: 20; Solvent:DMSO, Max Conc. mg/mL: 25.13, Max Conc. mM: 100 Poids moléculaire 251.280 g/mol XLogP3 3.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 3 Exact Mass 251.095 Da Monoisotopic Mass 251.095 Da Topological Polar Surface Area 42.100 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 325.000 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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