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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager 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.
Übersicht Urolithin D is competitive and reversible antagonist of EphA receptors. Urolithin D exhibits intra-classes selectivity.
Form:Solid
Specifications Synonyme
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- |
Spezifikationen & Reinheit
Moligand™, ≥99%
Biochemische und physiologische Mechanismen
Urolithin D is competitive and reversible antagonist of EphA receptors . Urolithin D exhibits intra-classes selectivity.
Storage
Protected from light,Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen Pubchem Sid 528767611 Kanonisches Lächeln 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 Isomere SMILES C1=CC(=C(C2=C1C3=CC(=C(C=C3C(=O)O2)O)O)O)O Alternative CAS-Nummer 131086-98-1 MeSH-Eintrag urolithin D Molekulargewicht 260.20
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 Klasse 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 Beschreibung 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Schmelzpunkt (°C) >227 °C Molekulargewicht 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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