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· · COA & SDS available for every product · Same-day shipping on in-stock items sorbinil - Moligand™,≥98% , Aldose reductase inhibitor, CAS No.68367-52-2, Aldose reductase inhibitor
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
Q1259458 | SORBINIL [WHO-DD] | CCG-221489 | Sorbinilo | Sorbinilo [Spanish] | (4S)-6-fluorospiro[2,3-dihydrochromene-4,5'-imidazolidine]-2',4'-dione | HMS3260F11 | NSC 355082 | Sorbinil [USAN:INN:BAN] | Sorbinilum [Latin] | Sorbinil | (S)-6-Fluorospiro(ch
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 Synonyms
Q1259458 | SORBINIL [WHO-DD] | CCG-221489 | Sorbinilo | Sorbinilo [Spanish] | (4S)-6-fluorospiro[2, 3-dihydrochromene-4, 5'-imidazolidine]-2', 4'-dione | HMS3260F11 | NSC 355082 | Sorbinil [USAN:INN:BAN] | Sorbinilum [Latin] | Sorbinil | (S)-6-Fluorospiro(ch
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Sorbinil is an aldose reductase inhibitor (ARI) that prevents the accumulation of sorbitol in cells or animals. Sorbinil is useful in studying diabetes and diabetic complications, reducing AR activity and inhibiting the polyol pathway.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Aldose reductase inhibitor
Names and Identifiers Canonical Smiles C1COC2=C(C13C(=O)NC(=O)N3)C=C(C=C2)F IUPAC Name (4S)-6-fluorospiro[2,3-dihydrochromene-4,5'-imidazolidine]-2',4'-dione InChIKey LXANPKRCLVQAOG-NSHDSACASA-N INCHI 1S/C11H9FN2O3/c12-6-1-2-8-7(5-6)11(3-4-17-8)9(15)13-10(16)14-11/h1-2,5H,3-4H2,(H2,13,14,15,16)/t11-/m0/s1 Isomeric SMILES C1COC2=C([C@]13C(=O)NC(=O)N3)C=C(C=C2)F WGK Germany 3 Molecular Weight 236.20 Reaxy-Rn 1083383 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1083383&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 Class Azolidines Subclass Imidazolidines Intermediate Tree Nodes Imidazolidinones - Imidazolidinediones Direct Parent Hydantoins Alternative Parents 1-benzopyrans Alpha amino acids and derivatives 5-monosubstituted hydantoins Alkyl aryl ethers N-acyl ureas Aryl fluorides Benzenoids Dicarboximides Azacyclic compounds Oxacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organofluorides Organonitrogen compounds Organopnictogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Hydantoin - Alpha-amino acid or derivatives - Chromane - 1-benzopyran - Benzopyran - 5-monosubstituted hydantoin - Alkyl aryl ether - N-acyl urea - Ureide - Aryl fluoride - Aryl halide - Benzenoid - Dicarboximide - Carbonic acid derivative - Urea - Carboxylic acid derivative - Oxacycle - Ether - Azacycle - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as hydantoins. These are heterocyclic compounds containing an imidazolidine substituted by ketone group at positions 2 and 4. External Descriptors organofluorine compound - imidazolidinone - azaspiro compound - chromanes - oxaspiro compound 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 236.200 g/mol XLogP3 0.700 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 0 Exact Mass 236.06 Da Monoisotopic Mass 236.06 Da Topological Polar Surface Area 67.400 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 376.000 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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