Eriodictyol - Moligand™, ≥98% , CAS No.552-58-9

CAS: 552-58-9 Cat. No.: E138993 Formula: C₁₅H₁₂O₆ Peso molecolare: 288.25 Beilstein Registry Number: 5104930 Numero EC: 209-016-4

GRADE & PURITY Moligand™, ≥98%

Synonyms

(2S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one | Eriodictyol, >=95.0% (HPLC) | (2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one | (S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one | Eriodic

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Application:
Eriodictyol, a flavonoid extracted from yerba santa, has anti-inflammatory and antioxidant activities and taste-modifying properties.

Specifications

Sinonimi

(2S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one | Eriodictyol, >=95.0% (HPLC) | (2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one | (S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one | Eriodic

Specifiche e purezza

Moligand™, ≥98%

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.

Grado

Moligand™

Tipo di azione

INHIBITOR

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 504758738
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504758738
• Sorrisi canonici: C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O
• IUPAC Name: (2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one
• InChIKey: SBHXYTNGIZCORC-ZDUSSCGKSA-N
• INCHI: 1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1
• Isomeri SMILES: C1[C@H](OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O
• WGK Germania: 3
• Peso molecolare: 288.25
• Beilstein: 5104930
• Reaxy-Rn: 385125
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=385125&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Classe Flavonoids
      • Subclass Flavans

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Classe: Flavonoids
• Subclass: Flavans
• Intermediate Tree Nodes: Not available
• Direct Parent: Flavanones
• Alternative Parents: 7-hydroxyflavonoids 5-hydroxyflavonoids 4'-hydroxyflavonoids 3'-hydroxyflavonoids Chromones Catechols Aryl alkyl ketones Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Vinylogous acids Oxacyclic compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Flavanone - 3'-hydroxyflavonoid - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Chromone - Benzopyran - Chromane - 1-benzopyran - Catechol - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-2-unsubstituted benzenoid - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Ketone - Organoheterocyclic compound - Oxacycle - Ether - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as flavanones. These are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3.
• External Descriptors: Flavanones

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.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

CA4 Tclin Carbonic anhydrase 4 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA12 Tclin Carbonic anhydrase 12 (1 Activities)

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CA7 Tclin Carbonic anhydrase 7 (1 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TYR Tclin Tyrosinase (717 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

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XDH Tclin Xanthine dehydrogenase (1038 Activities)

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CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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BCHE Tclin Butyrylcholinesterase (7174 Activities)

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CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FBP1 Tchem Fructose-1,6-bisphosphatase (1199 Activities)

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CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

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FLT3 Tclin Tyrosine-protein kinase receptor FLT3 (13481 Activities)

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THP-1 (11052 Activities)

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U-937 (7138 Activities)

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Col2 (437 Activities)

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HEK293 (82097 Activities)

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Monocyte (474 Activities)

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HUVEC (11049 Activities)

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KB (17409 Activities)

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LNCaP (8286 Activities)

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MDA-MB-435 (38290 Activities)

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Lu1 (576 Activities)

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PSMB5 Tclin Proteasome Macropain subunit MB1 (2451 Activities)

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SETD7 Tchem Histone-lysine N-methyltransferase SETD7 (390 Activities)

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SLCO2B1 Tchem Solute carrier organic anion transporter family member 2B1 (580 Activities)

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IPMK Tbio Inositol polyphosphate multikinase (34 Activities)

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Obiettivi associati (non umani)

Ca7 Carbonic anhydrase VII (3 Activities)

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CA4 Carbonic anhydrase IV (1713 Activities)

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Cryz Quinone oxidoreductase (288 Activities)

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Helicobacter pylori (3113 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Proteus mirabilis (3894 Activities)

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Enterococcus faecalis (29875 Activities)

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Trypanosoma brucei brucei (13300 Activities)

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Plasmodium falciparum (966862 Activities)

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Leishmania donovani (89745 Activities)

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Leishmania mexicana (936 Activities)

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Mus musculus (284745 Activities)

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3T3-L1 (3664 Activities)

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H9c2 (3506 Activities)

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J774.A1 (2436 Activities)

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RAW264.7 (28094 Activities)

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Vero (26788 Activities)

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HT-22 (3261 Activities)

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L929 (3802 Activities)

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BCHE Cholinesterase (8742 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Thoracic aorta (838 Activities)

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Ip6k2 Inositol hexakisphosphate kinase 2 (3 Activities)

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: sensitive to light
• Peso molecolare: 288.250 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 288.063 Da
• Monoisotopic Mass: 288.063 Da
• Topological Polar Surface Area: 107.000 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 400.000
• 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

Riferimenti

1. Wan-Ling Cai, Ling Liu, Xue-Qing Liao, Kai-Li Tao, Fang Feng, Gong-Jun Yang.  (2016)  Determination of Eriodictyol by a Modified Multi-Walled Carbon Nanotube Glassy Carbon Electrode.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2015.1113423]

2. Xia Yang, Yun Wang, Yan Sun, Jiali Guo, Zhaojun Geng, Bingyao Wei, Peiqin Li, Guanghui Tang.  (2025)  Integrated transcriptomics and metabolomics revealed the role of the flavonoid pathway in the resistance of Zanthoxylum bungeanum against leaf rust.  SCIENTIA HORTICULTURAE,      [PMID:] [10.1016/j.scienta.2025.113990]

3. Hongbiao Li, Shuai Zhang, Zilong Dong, Xiaoyu Shan, Jingwen Zhou, Weizhu Zeng.  (2024)  De Novo Biosynthesis of Dihydroquercetin in Saccharomyces cerevisiae.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:39180741] [10.1021/acs.jafc.4c05546]

Domande frequenti

What is the purity of this product?

This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at ?20 °C, protected from light. The material is light-sensitive — keep it in its original opaque or amber container.

How is this product shipped?

This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 552-58-9, the molecular formula is C15H12O6, and the molecular weight is 288.25 g/mol. InChIKey SBHXYTNGIZCORC-ZDUSSCGKSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.