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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items ML 354 - Moligand™, ≥98%(HPLC) , Antagonist of PAR4, CAS No.89159-60-4, Antagonist of PAR4
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. ≥98%(HPLC) Synonyms
1-Methyl-5-nitro-3-phenyl-1H-indole-2-methanol | DTXSID90353779 | 1h-indole-2-methanol, 1-methyl-5-nitro-3-phenyl- | ML 354;ML-354 | STK783537 | EU-0047807 | HY-19973 | SR-01000083946 | Oprea1_017031 | 1-methyl-2-hydroxymethyl-3-phenyl-5-nitroindole | VU0
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98%(HPLC) Moligand™ 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 Sinónimos
1-Methyl-5-nitro-3-phenyl-1H-indole-2-methanol | DTXSID90353779 | 1h-indole-2-methanol, 1-methyl-5-nitro-3-phenyl- | ML 354;ML-354 | STK783537 | EU-0047807 | HY-19973 | SR-01000083946 | Oprea1_017031 | 1-methyl-2-hydroxymethyl-3-phenyl-5-nitroindole | VU0
Especificaciones y pureza
Moligand™, ≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Selective PAR4antagonist (IC50= 140 nM). Exhibits 70-fold selectivity for PAR4over PAR1.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Antagonist of PAR4
Nombres e identificadores Sonrisas canónicas CN1C2=C(C=C(C=C2)[N+](=O)[O-])C(=C1CO)C3=CC=CC=C3 IUPAC Name (1-methyl-5-nitro-3-phenylindol-2-yl)methanol InChIKey GNJUKVGDCUKDLF-UHFFFAOYSA-N INCHI 1S/C16H14N2O3/c1-17-14-8-7-12(18(20)21)9-13(14)16(15(17)10-19)11-5-3-2-4-6-11/h2-9,19H,10H2,1H3 Isómeros SMILES CN1C2=C(C=C(C=C2)[N+](=O)[O-])C(=C1CO)C3=CC=CC=C3 CAS alternativo 89159-60-4 Términos de entrada MeSH ML354 compound;VU0099704 Peso molecular 282.29 Reaxy-Rn 4503021 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4503021&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 Clase Pyrroles Subclass Substituted pyrroles Intermediate Tree Nodes Not available Direct Parent Phenylpyrroles Alternative Parents N-alkylindoles Indoles Nitroaromatic compounds Benzene and substituted derivatives N-methylpyrroles Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic oxides Organic zwitterions Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Primary alcohols Aromatic alcohols Molecular Framework Aromatic heteropolycyclic compounds Substituents 3-phenylpyrrole - N-alkylindole - Indole - Indole or derivatives - Nitroaromatic compound - Monocyclic benzene moiety - N-methylpyrrole - Benzenoid - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Aromatic alcohol - Organic zwitterion - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as phenylpyrroles. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrole ring through a CC or CN bond. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:DMSO, Max Conc. mg/mL: 28.23, Max Conc. mM: 100 Peso molecular 282.290 g/mol XLogP3 2.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 2 Exact Mass 282.1 Da Monoisotopic Mass 282.1 Da Topological Polar Surface Area 71.000 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 378.000 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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Reconstitution Calculator Reseñas Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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