Enocyanin , CAS No.11029-12-2

CAS: 11029-12-2 Cat. No.: E648339 EG-Nummer: 600-954-3

Synonyms

Flavylium | Q-200643 | Anthocyanidins | CHEBI:36121 | 2-phenylchromenylium | Q27116709 | 2-phenyl-1$l^{4}-chromen-1-ylium | InChI=1/C15H11O/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H/q+ | UNII-F02KPB2508 | Enocyanin | F02KPB2508 | Oenocyanin |

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Enocyanin is an anthocyanin extracted from grapes. Enocyanin shows inhibitory effect on the leucine aminopeptidase , acid phosphatase , γ-glutamyl transpeptidase and esterase activity

In Vitro

Enocyanin (0.1%) affects the leucine aminopeptidase, acid phosphatase, γ-glutamyl transpeptidase and esterase activity by 63%, 100%, 134% and 99%, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:Acid phosphatase

Spezifikationen

Synonyme

Flavylium | Q-200643 | Anthocyanidins | CHEBI:36121 | 2-phenylchromenylium | Q27116709 | 2-phenyl-1$l^{4}-chromen-1-ylium | InChI=1/C15H11O/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H/q+ | UNII-F02KPB2508 | Enocyanin | F02KPB2508 | Oenocyanin |

Biochemische und physiologische Mechanismen

Enocyanin is an anthocyanin extracted from grapes. Enocyanin shows inhibitory effect on the leucine aminopeptidase , acid phosphatase , γ-glutamyl transpeptidase and esterase activity.

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Namen und Kennungen

Kanonisches Lächeln

C1=CC=C(C=C1)C2=[O+]C3=CC=CC=C3C=C2

IUPAC Name

2-phenylchromenylium

InChIKey

NWKFECICNXDNOQ-UHFFFAOYSA-N

INCHI

1S/C15H11O/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H/q+1

Isomere SMILES

C1=CC=C(C=C1)C2=[O+]C3=CC=CC=C3C=C2

Alternative CAS-Nummer

11029-12-2,14051-53-7

MeSH-Eintrag

Anthocyanidin;Anthocyanidins;Anthocyanin;Anthocyanins;Leucoanthocyanidins

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Klasse Flavonoids
      • Subclass Anthocyanidins

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Klasse: Flavonoids
• Subclass: Anthocyanidins
• Intermediate Tree Nodes: Not available
• Direct Parent: Anthocyanidins
• Alternative Parents: 1-benzopyrans Benzene and substituted derivatives Heteroaromatic compounds Oxacyclic compounds Organooxygen compounds Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Anthocyanidin - 1-benzopyran - Benzopyran - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic cation - Aromatic heteropolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as anthocyanidins. These are sugar-free counterparts of anthocyanins based on the flavylium ion or 2-phenylchromenylium ion.
• External Descriptors: chromenyliums

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

Chemische und physikalische Eigenschaften

• Löslichkeit: DMSO : ≥ 50 mg/mL H2O : 5 mg/mL (Need ultrasonic)
• Molekulargewicht: 207.250 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 207.081 Da
• Monoisotopic Mass: 207.081 Da
• Topological Polar Surface Area: 1.000 Ų
• Heavy Atom Count: 16
• Formal Charge: 1
• Complexity: 219.000
• 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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