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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Delpazolid - Moligand™, ≥98% , Bacterial 70S ribosome inhibitor, CAS No.1219707-39-7, Bacterial 70S ribosome inhibitor
Disponível para encomenda
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% Synonyms
2-Oxazolidinone, 3-(4-(5,6-dihydro-1-methyl-1,2,4-triazin-4(1H)-yl)-3-fluorophenyl)-5-(hydroxymethyl)-, (5R)- | 4-Methylbenzenethiol, 98% | (5R)-3-(3-Fluoro-4-(1-methyl-5,6-dihydro-1,2,4-triazin-4(1H)-yl)phenyl)-5-(hydroxymethyl)-1,3-oxazolidin-2-one | (5
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98% 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
2-Oxazolidinone, 3-(4-(5,6-dihydro-1-methyl-1,2,4-triazin-4(1H)-yl)-3-fluorophenyl)-5-(hydroxymethyl)-, (5R)- | 4-Methylbenzenethiol, 98% | (5R)-3-(3-Fluoro-4-(1-methyl-5,6-dihydro-1,2,4-triazin-4(1H)-yl)phenyl)-5-(hydroxymethyl)-1,3-oxazolidin-2-one | (5
Especificações e pureza
Moligand™, ≥98%
Mecanismos bioquímicos e fisiológicos
Delpazolid (LCB01-0371), a novel oxazolidinone antibiotic agent, is an inhibitor of the growth of\xa0MSSA\xa0and\xa0MRSA\xa0with MIC90 of 2 μg/mL for both of them.
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Mecanismo de ação
Bacterial 70S ribosome inhibitor
Propriedades do produto Nomes e identificadores Pubchem Sid 528771841 Sorrisos canónicos CN1CCN(C=N1)C2=C(C=C(C=C2)N3CC(OC3=O)CO)F IUPAC Name (5R)-3-[3-fluoro-4-(1-methyl-5,6-dihydro-1,2,4-triazin-4-yl)phenyl]-5-(hydroxymethyl)-1,3-oxazolidin-2-one InChIKey QLUWQAFDTNAYPN-LLVKDONJSA-N INCHI 1S/C14H17FN4O3/c1-17-4-5-18(9-16-17)13-3-2-10(6-12(13)15)19-7-11(8-20)22-14(19)21/h2-3,6,9,11,20H,4-5,7-8H2,1H3/t11-/m1/s1 SMILES isoméricas CN1CCN(C=N1)C2=C(C=C(C=C2)N3C[C@@H](OC3=O)CO)F Peso molecular 308.31 Reaxy-Rn 55895677 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=55895677&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 Benzenoids Classe Benzene and substituted derivatives Subclass Aniline and substituted anilines Intermediate Tree Nodes Not available Direct Parent Aniline and substituted anilines Alternative Parents Fluorobenzenes 1,2,4-triazines Oxazolidinones Aryl fluorides Carbamate esters Tertiary amines Amidrazones Oxacyclic compounds Azacyclic compounds Formamidines Hydrazones Organic oxides Carbonyl compounds Hydrocarbon derivatives Organofluorides Primary alcohols Molecular Framework Aromatic heteromonocyclic compounds Substituents Aniline or substituted anilines - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Oxazolidinone - Triazine - 1,2,4-triazine - Oxazolidine - Carbamic acid ester - Tertiary amine - Carboxylic acid amidrazone - Amidine - Oxacycle - Azacycle - Organoheterocyclic compound - Formamidine - Hydrazone - Primary alcohol - Organofluoride - Organohalogen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Aromatic heteromonocyclic compound Descrição This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety. 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.
Estrutura 3D Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Peso molecular 308.310 g/mol XLogP3 0.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 3 Exact Mass 308.128 Da Monoisotopic Mass 308.128 Da Topological Polar Surface Area 68.600 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 450.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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