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Home > Encyclopedia > Licorisoflavan A

Licorisoflavan A

Licorisoflavan A structure

Licorisoflavan A 

structure
  • CAS No:

    129314-37-0

  • Formula:

    C27H34O5

  • Chemical Name:

    Licorisoflavan A

  • Synonyms:

    1,3-Benzenediol,4-[(3R)-3,4-dihydro-5,7-dimethoxy-6-(3-methyl-2-buten-1-yl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-buten-1-yl)-;1,3-Benzenediol,4-[3,4-dihydro-5,7-dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-butenyl)-,(R)-;1,3-Benzenediol,4-[(3R)-3,4-dihydro-5,7-dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-butenyl)-;4-[(3R)-3,4-Dihydro-5,7-dimethoxy-6-(3-methyl-2-buten-1-yl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-buten-1-yl)-1,3-benzenediol;(+)-7-O-Methyllicoricidin;7-O-Methyllicoricidin;Licorisoflavan A;7-O-Methyllicorisoflavan B

  • Categories:

    Natural Products  >  Flavonoids

Description

ChEBI: A member of the class of hydroxyisoflavans that is the 7-O-methyl derivative of licoricidin. Isolated from Glycyrrhiza uralensis, it exhibits antibacterial activity.


Licorisoflavan A is a member of the class of hydroxyisoflavans that is the 7-O-methyl derivative of licoricidin. Isolated from Glycyrrhiza uralensis, it exhibits antibacterial activity. It has a role as an antibacterial agent and a plant metabolite. It is an aromatic ether, a member of hydroxyisoflavans and a methoxyisoflavan. It derives from a licoricidin.

Licorisoflavan A Basic Attributes

438.564

438.56

DTXSID40156136

Characteristics

68.2

6.54

1.130±0.06 g/cm3(Predicted)

589.2±50.0 °C(Predicted)

310.1±30.1 °C

1.576

1.77E-14mmHg at 25°C

Drug Information

5-O-methyllicoricidin

Computed Properties

Molecular Weight:438.6
XLogP3:6.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:438.24062418
Monoisotopic Mass:438.24062418
Topological Polar Surface Area:68.2
Heavy Atom Count:32
Complexity:650
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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