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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque cefiderocol - Moligand™, ≥95% , Bacterial penicillin-binding protein inhibitor, CAS No.1225208-94-5, Bacterial penicillin-binding protein 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. ≥95% Synonyms
BS-14716 | cefiderocolum | EN300-22213856 | RSC 649266 | (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-3-[[1-[2-[(2-chloro-3,4-dihydroxybenzoyl)amino]ethyl]pyrrolidin-1-ium-1-yl]methyl]-8-oxo-5-thia-1-azabicyc
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥95% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Argon charged 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.
Visão geral Cefiderocol (S-649266) is a siderophore cephalosporin which has a potent activity against a broad range of aerobic Gram-negative bacterial species with MIC50s of 2 μg/mL or less.
Specifications Sinónimos
BS-14716 | cefiderocolum | EN300-22213856 | RSC 649266 | (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-3-[[1-[2-[(2-chloro-3,4-dihydroxybenzoyl)amino]ethyl]pyrrolidin-1-ium-1-yl]methyl]-8-oxo-5-thia-1-azabicyc
Especificações e pureza
Moligand™, ≥95%
Condições de armazenamento de armazenamento
Store at -20°C,Argon charged
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 penicillin-binding protein inhibitor
Propriedades do produto Nomes e identificadores Pubchem Sid 528768661 Sorrisos canónicos CC(C)(C(=O)O)ON=C(C1=CSC(=N1)N)C(=O)NC2C3N(C2=O)C(=C(CS3)C[N+]4(CCCC4)CCNC(=O)C5=C(C(=C(C=C5)O)O)Cl)C(=O)[O-] IUPAC Name (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-3-[[1-[2-[(2-chloro-3,4-dihydroxybenzoyl)amino]ethyl]pyrrolidin-1-ium-1-yl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate InChIKey DBPPRLRVDVJOCL-FQRUVTKNSA-N INCHI 1S/C30H34ClN7O10S2/c1-30(2,28(46)47)48-36-19(16-13-50-29(32)34-16)24(42)35-20-25(43)37-21(27(44)45)14(12-49-26(20)37)11-38(8-3-4-9-38)10-7-33-23(41)15-5-6-17(39)22(40)18(15)31/h5-6,13,20,26H,3-4,7-12H2,1-2H3,(H7-,32,33,34,35,36,39,40,41,42,44,45,46,47)/t20-,26-/m1/s1 SMILES isoméricas CC(C)(C(=O)O)O/N=C(/C1=CSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C[N+]4(CCCC4)CCNC(=O)C5=C(C(=C(C=C5)O)O)Cl)C(=O)[O-] CAS alternativo 1225208-94-5 PubChem CID 77843966 Termos de entrada MeSH cefiderocol;S-649266 Peso molecular 752.21
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 Lactams Subclass Beta lactams Intermediate Tree Nodes Cephems - Cephalosporins Direct Parent 3'-quaternary ammonium cephalosporins Alternative Parents N-acyl-alpha amino acids and derivatives 2-halobenzoic acids and derivatives Benzamides 3-chlorocatechols Benzoyl derivatives M-chlorophenols O-chlorophenols Chlorobenzenes 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids 2,4-disubstituted thiazoles 1,3-thiazines Aryl chlorides Dicarboxylic acids and derivatives 2-amino-1,3-thiazoles N-alkylpyrrolidines Tetraalkylammonium salts Heteroaromatic compounds Tertiary carboxylic acid amides Vinylogous halides Azetidines Amino acids Secondary carboxylic acid amides Carboxylic acid salts Thiohemiaminal derivatives Dialkylthioethers Carboxylic acids Azacyclic compounds Hydrocarbon derivatives Organic oxides Organic salts Primary amines Organochlorides Organic zwitterions Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents 3'-quaternary ammonium cephalosporin - N-acyl-alpha amino acid or derivatives - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Alpha-amino acid or derivatives - Benzamide - 3-chlorocatechol - Chlorocatechol - Benzoic acid or derivatives - 2-chlorophenol - 3-chlorophenol - 2-halophenol - 3-halophenol - Benzoyl - Catechol - 2,4-disubstituted 1,3-thiazole - 1-hydroxy-2-unsubstituted benzenoid - Halobenzene - Phenol - Chlorobenzene - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Aryl chloride - N-alkylpyrrolidine - Monocyclic benzene moiety - Meta-thiazine - Aryl halide - Dicarboxylic acid or derivatives - 1,3-thiazol-2-amine - Tetraalkylammonium salt - Heteroaromatic compound - Vinylogous halide - Thiazole - Tertiary carboxylic acid amide - Quaternary ammonium salt - Pyrrolidine - Azole - Amino acid or derivatives - Carboxamide group - Carboxylic acid salt - Secondary carboxylic acid amide - Amino acid - Azetidine - Hemithioaminal - Dialkylthioether - Thioether - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organic nitrogen compound - Carbonyl group - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Primary amine - Organic zwitterion - Organic salt - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound Descrição This compound belongs to the class of organic compounds known as 3'-quaternary ammonium cephalosporins. These are cephalosporins that are substituted at the 3'-position by a quaternary ammonium 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.
Estrutura 3D Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Peso molecular 752.200 g/mol XLogP3 1.000 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 15 Rotatable Bond Count 12 Exact Mass 751.15 Da Monoisotopic Mass 751.15 Da Topological Polar Surface Area 310.000 Ų Heavy Atom Count 50 Formal Charge 0 Complexity 1440.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
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