5,7-Dihydroxychromone - 10mM in DMSO , CAS No.31721-94-5

CAS: 31721-94-5 Cat. No.: D580284 Formule: C₉H₆O₄ Poids moléculaire: 178.14

GRADE & PURITY 10mM in DMSO

Synonyms

DHC | FT-0686568 | 5,7-dihydroxychromen-4-one | 5,7-Dihydroxychromone | AC-6025 | F17673 | C09001 | Q-100396 | Q27105540 | AKOS015999181 | DTXSID30185617 | SCHEMBL1860859 | 5,7-Dihydroxy-4-chromone | B7S | MS-22951 | 5,7-Dihydroxy-4H-1-benzopyran-4-one |

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonymes

DHC | FT-0686568 | 5,7-dihydroxychromen-4-one | 5,7-Dihydroxychromone | AC-6025 | F17673 | C09001 | Q-100396 | Q27105540 | AKOS015999181 | DTXSID30185617 | SCHEMBL1860859 | 5,7-Dihydroxy-4-chromone | B7S | MS-22951 | 5,7-Dihydroxy-4H-1-benzopyran-4-one |

Spécifications et pureté

10mM in DMSO

Mécanismes biochimiques et physiologiques

5,7-Dihydroxychromone, the extract of Cudrania tricuspidata, activates Nrf2/ARE signal and exerts neuroprotective effects against 6-hydroxydopamine (6-OHDA)-induced oxidative stress and apoptosis. 5,7-Dihydroxychromone inhibits the expression of activated

Conditions de stockage de stockage

Store at -80°C

Expédié en

Dry ice packs + Cold packs

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

ACTIVATOR

Noms et identifiants

• Pubchem Sid: 528761178
• Sourires canoniques: C1=COC2=CC(=CC(=C2C1=O)O)O
• IUPAC Name: 5,7-dihydroxychromen-4-one
• InChIKey: NYCXYKOXLNBYID-UHFFFAOYSA-N
• INCHI: 1S/C9H6O4/c10-5-3-7(12)9-6(11)1-2-13-8(9)4-5/h1-4,10,12H
• Isomères SMILES: C1=COC2=CC(=CC(=C2C1=O)O)O
• Poids moléculaire: 178.14
• Reaxy-Rn: 154579
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=154579&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Benzopyrans
      • Subclass 1-benzopyrans

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Benzopyrans
• Subclass: 1-benzopyrans
• Intermediate Tree Nodes: Not available
• Direct Parent: Chromones
• Alternative Parents: Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Heteroaromatic compounds Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Chromone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Benzenoid - Pyran - Heteroaromatic compound - Vinylogous acid - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as chromones. These are compounds containing a benzopyran-4-one moiety.
• External Descriptors: chromones

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

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: insoluble in H2O; ≥5.41 mg/mL in EtOH with gentle warming; ≥7.05 mg/mL in DMSO
• Sensibilité: Light sensitive
• Poids moléculaire: 178.140 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 178.027 Da
• Monoisotopic Mass: 178.027 Da
• Topological Polar Surface Area: 66.800 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 248.000
• 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

Références

1. Wang Baolin, Wang Qinqin, Yuan Renyikun, Yang Shilin, Lu Meilin, Yuan Fuhong, Dong Zhidan, Mo Menghuan, Pan Qiming, Gao Hongwei.  (2023)  Prenylated chromones and flavonoids isolated from the roots of Flemingia macrophylla and their anti-lung cancer activity.  Chinese Medicine,  18  (1): (1-14).  [PMID:37996917] [10.1186/s13020-023-00860-3]