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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Celgosivir - ≥98% , Alpha glucosidase inhibitor, CAS No.121104-96-9, Alpha glucosidase inhibitor
Synonyms
DB06580 | (1S,6S,7S,8R,8aR)-Octahydro-1,7,8-trihydroxy-6-indolizinyl butyrate | 6-O-Butanoylcastanospermine | BuCast | SCHEMBL135812 | VIR-222 | 6-Butyryl castanospermine | MBI 3253; MDL 28574; MX3253 | Butanoic acid, octahydro-1,7,8-trihydroxy-6-indolizi
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% 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.
Descripción general Celgosivir is an α-glucosidase I inhibitor that can be studied for its potential use in the treatment of HCV infection.
Specifications Sinónimos
DB06580 | (1S, 6S, 7S, 8R, 8aR)-Octahydro-1, 7, 8-trihydroxy-6-indolizinyl butyrate | 6-O-Butanoylcastanospermine | BuCast | SCHEMBL135812 | VIR-222 | 6-Butyryl castanospermine | MBI 3253; MDL 28574; MX3253 | Butanoic acid, octahydro-1, 7, 8-trihydroxy-6-indolizi
Especificaciones y pureza
≥98%
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
Alpha glucosidase inhibitor
Propiedades del producto Nombres e identificadores Sonrisas canónicas CCCC(=O)OC1CN2CCC(C2C(C1O)O)O IUPAC Name [(1S,6S,7S,8R,8aR)-1,7,8-trihydroxy-1,2,3,5,6,7,8,8a-octahydroindolizin-6-yl] butanoate InChIKey HTJGLYIJVSDQAE-VWNXEWBOSA-N INCHI 1S/C12H21NO5/c1-2-3-9(15)18-8-6-13-5-4-7(14)10(13)12(17)11(8)16/h7-8,10-12,14,16-17H,2-6H2,1H3/t7-,8-,10+,11+,12+/m0/s1 Isómeros SMILES CCCC(=O)O[C@H]1CN2CC[C@@H]([C@@H]2[C@H]([C@@H]1O)O)O Peso molecular 259.3 Reaxy-Rn 13566658 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13566658&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 Indolizidines Subclass Not available Intermediate Tree Nodes Not available Direct Parent Indolizidines Alternative Parents Fatty acid esters Piperidines N-alkylpyrrolidines Trialkylamines Secondary alcohols Carboxylic acid esters Amino acids and derivatives 1,2-aminoalcohols Polyols Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteropolycyclic compounds Substituents Indolizidine - Fatty acid ester - Piperidine - N-alkylpyrrolidine - Fatty acyl - Pyrrolidine - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-aminoalcohol - Carboxylic acid ester - Azacycle - Carboxylic acid derivative - Polyol - Monocarboxylic acid or derivatives - Organopnictogen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Alcohol - Carbonyl group - Amine - Hydrocarbon derivative - Organic oxide - Aliphatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen. 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) Propiedades químicas y físicas Solubilidad Soluble in DMSO. Índice de refracción n20D1.57 (Predicted) Punto de ebullición (°C) 422.9° C Punto de fusión (°C) 147.02° C Peso molecular 259.300 g/mol XLogP3 -0.800 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 4 Exact Mass 259.142 Da Monoisotopic Mass 259.142 Da Topological Polar Surface Area 90.200 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 311.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 5 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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