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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Lff-571 , Elongation factor Tu inhibitor, CAS No.1160959-55-6, Elongation factor Tu inhibitor
Synonyms
LFF-571 | DB13013 | J3.333.591A | Q27292430 | SCHEMBL18391833 | W7AUL2R95Z | CHEMBL2063705 | UNII-W7AUL2R95Z | AKOS040748742 | LFF571 | HY-19906 | 3u2q | LFF 571 | SCHEMBL18392088
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Why this grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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
LFF-571 | DB13013 | J3.333.591A | Q27292430 | SCHEMBL18391833 | W7AUL2R95Z | CHEMBL2063705 | UNII-W7AUL2R95Z | AKOS040748742 | LFF571 | HY-19906 | 3u2q | LFF 571 | SCHEMBL18392088
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Elongation factor Tu inhibitor
Propiedades del producto Nombres e identificadores Sonrisas canónicas CC1=C2C(=O)NC(C3=NC(=C(S3)COC)C(=O)NCC(=O)NC(C4=NC(=CS4)C5=NC(=CS5)C6=C(C=CC(=N6)C7=NC(=CS7)N(CCCCC(=O)O)C(=O)OC8CCC(CC8)C(=O)O)C9=NC(=CS9)C(=O)NC(C(=N2)S1)CC(=O)NC)C(C1=CC=CC=C1)O)C(C)C IUPAC Name 4-[4-carboxybutyl-[2-[(18S,25S,35S)-35-[(S)-hydroxy(phenyl)methyl]-28-(methoxymethyl)-21-methyl-18-[2-(methylamino)-2-oxoethyl]-16,23,30,33-tetraoxo-25-propan-2-yl-3,13,20,27,37-pentathia-7,17,24,31,34,39,40,41,42,43-decazaheptacyclo[34.2.1.12,5.112,15.11 InChIKey GNLYKLDXQZHYTR-QWSGWXDSSA-N INCHI 1S/C60H63N13O13S6/c1-28(2)44-58-72-47(39(92-58)23-85-5)51(80)62-22-42(75)69-48(49(78)30-11-7-6-8-12-30)57-67-38(26-89-57)55-65-36(24-88-55)46-33(53-66-37(25-87-53)50(79)64-35(21-41(74)61-4)56-71-45(29(3)91-56)52(81)70-44)18-19-34(63-46)54-68-40(27-9 Isómeros SMILES CC1=C2C(=O)N[C@H](C3=NC(=C(S3)COC)C(=O)NCC(=O)N[C@H](C4=NC(=CS4)C5=NC(=CS5)C6=C(C=CC(=N6)C7=NC(=CS7)N(CCCCC(=O)O)C(=O)OC8CCC(CC8)C(=O)O)C9=NC(=CS9)C(=O)N[C@H](C(=N2)S1)CC(=O)NC)[C@H](C1=CC=CC=C1)O)C(C)C PubChem CID 42638236 Peso molecular 1366.6
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 Clase Macrolactams Subclass Not available Intermediate Tree Nodes Not available Direct Parent Macrolactams Alternative Parents Beta amino acids and derivatives Alpha amino acids and derivatives Thiazolecarboxylic acids and derivatives 2-heteroaryl carboxamides 2,4-disubstituted thiazoles Pyridines and derivatives Imidolactams Dicarboxylic acids and derivatives Benzene and substituted derivatives Heteroaromatic compounds Carbamate esters Tertiary amines Secondary carboxylic acid amides Secondary alcohols Lactams Amino acids Dialkyl ethers Carboxylic acids Azacyclic compounds Hydrocarbon derivatives Aromatic alcohols Organic oxides Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Macrolactam - Beta amino acid or derivatives - Alpha-amino acid or derivatives - 2-heteroaryl carboxamide - Thiazolecarboxylic acid or derivatives - 2,4-disubstituted 1,3-thiazole - Dicarboxylic acid or derivatives - Pyridine - Monocyclic benzene moiety - Imidolactam - Benzenoid - Azole - Heteroaromatic compound - Thiazole - Carbamic acid ester - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Amino acid - Lactam - Amino acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Ether - Azacycle - Dialkyl ether - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Aromatic alcohol - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Alcohol - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. 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 (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
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