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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel Gentisein - Moligand™,≥98% , CAS No.529-49-7
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
1,3,7-Trihydroxy-xanthen-9-one | 1,3,7-trihydroxyxanthen-9-one | BRN 0384687 | 1,3,7-trihydroxy-9H-xanthen-9-one | 0P3G42TQ63 | Gentisein | 9H-Xanthen-9-one, 1,3,7-trihydroxy- | BDBM50155446 | NSC 329491 | Q27106719 | AKOS022662257 | CHEBI:5323 | Gentisei
Storage
Protected from light,Store at -20°C
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 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 Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC 50 value of 4.7 µM.
Form:Solid
Specifications Synonyme
1,3,7-Trihydroxy-xanthen-9-one | 1,3,7-trihydroxyxanthen-9-one | BRN 0384687 | 1,3,7-trihydroxy-9H-xanthen-9-one | 0P3G42TQ63 | Gentisein | 9H-Xanthen-9-one, 1,3,7-trihydroxy- | BDBM50155446 | NSC 329491 | Q27106719 | AKOS022662257 | CHEBI:5323 | Gentisei
Spezifikationen & Reinheit
Moligand™,≥98%
Biochemische und physiologische Mechanismen
Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC 50 value of 4.7 µM.
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 Kanonisches Lächeln
C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O
IUPAC Name
1,3,7-trihydroxyxanthen-9-one
InChIKey
JJUNZBRHHGLJQW-UHFFFAOYSA-N
INCHI
1S/C13H8O5/c14-6-1-2-10-8(3-6)13(17)12-9(16)4-7(15)5-11(12)18-10/h1-5,14-16H
Isomere SMILES
C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O
Alternative CAS-Nummer
529-49-7
MeSH-Eintrag
1,3,7-trihydroxy-xanthone;1,3,7-trihydroxyxanthone;gentisein
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 Klasse Benzopyrans Subclass 1-benzopyrans Intermediate Tree Nodes Dibenzopyrans - Xanthenes Direct Parent Xanthones Alternative Parents Chromones Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Heteroaromatic compounds Polyols Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Xanthone - Chromone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Pyran - Benzenoid - Heteroaromatic compound - Vinylogous acid - Polyol - Oxacycle - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. External Descriptors xanthenes 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 Löslichkeit DMSO : 100 mg/mL (409.50 mM; Need ultrasonic) Empfindlichkeit light sensitive Molekulargewicht 244.200 g/mol XLogP3 2.400 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 0 Exact Mass 244.037 Da Monoisotopic Mass 244.037 Da Topological Polar Surface Area 87.000 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 344.000 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 Bewertungen 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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