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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino Urolithin D - Moligand™, ≥99% , CAS No.131086-98-1
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. ≥99% Synonyms
3,4,8,9-Tetrahydroxy-6H-benzo[c]chromen-6-one | CHEBI:174390 | JVT9VXW2DJ | Urolithin-D | 6H-Dibenzo[b,d]pyran-6-one, 3,4,8,9-tetrahydroxy- | HY-133178 | 3,4,8,9-tetrahydroxy-6h-dibenzo[b,d]pyran-6-one | 6H-Dibenzo(b,d)pyran-6-one, 3,4,8,9-tetrahydroxy- |
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,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.
Panoramica Urolithin D is competitive and reversible antagonist of EphA receptors. Urolithin D exhibits intra-classes selectivity.
Form:Solid
Specifications Sinonimi
3,4,8,9-Tetrahydroxy-6H-benzo[c]chromen-6-one | CHEBI:174390 | JVT9VXW2DJ | Urolithin-D | 6H-Dibenzo[b,d]pyran-6-one, 3,4,8,9-tetrahydroxy- | HY-133178 | 3,4,8,9-tetrahydroxy-6h-dibenzo[b,d]pyran-6-one | 6H-Dibenzo(b,d)pyran-6-one, 3,4,8,9-tetrahydroxy- |
Specifiche e purezza
Moligand™, ≥99%
Meccanismi biochimici e fisiologici
Urolithin D is competitive and reversible antagonist of EphA receptors . Urolithin D exhibits intra-classes selectivity.
Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Pubchem Sid 528767611 Sorrisi canonici C1=CC(=C(C2=C1C3=CC(=C(C=C3C(=O)O2)O)O)O)O IUPAC Name 3,4,8,9-tetrahydroxybenzo[c]chromen-6-one InChIKey NEZDQSKPNPRYAW-UHFFFAOYSA-N INCHI 1S/C13H8O6/c14-8-2-1-5-6-3-9(15)10(16)4-7(6)13(18)19-12(5)11(8)17/h1-4,14-17H Isomeri SMILES C1=CC(=C(C2=C1C3=CC(=C(C=C3C(=O)O2)O)O)O)O CAS alternativo 131086-98-1 Termini MeSH urolithin D Peso molecolare 260.20
Documentazione 📋 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 Classe Coumarins and derivatives Subclass Hydroxycoumarins Intermediate Tree Nodes Not available Direct Parent 7,8-dihydroxycoumarins Alternative Parents Isocoumarins and derivatives 2-benzopyrans 1-benzopyrans Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Heteroaromatic compounds Lactones Polyols Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 7,8-dihydroxycoumarin - Isocoumarin - Benzopyran - 2-benzopyran - 1-benzopyran - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Benzenoid - Pyran - Heteroaromatic compound - Lactone - Oxacycle - Organoheterocyclic compound - Polyol - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound Descrizione This compound belongs to the class of organic compounds known as 7,8-dihydroxycoumarins. These are coumarins bearing two hydroxyl groups at the C7- and C8-positions of the coumarin skeleton, respectively. 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Punto di fusione (°C) >227 °C Peso molecolare 260.200 g/mol XLogP3 1.600 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 0 Exact Mass 260.032 Da Monoisotopic Mass 260.032 Da Topological Polar Surface Area 107.000 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 372.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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Reconstitution Calculator Recensioni Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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