ChemicalBook--->CAS DataBase List--->142628-53-3

142628-53-3

142628-53-3 Structure

142628-53-3 Structure
IdentificationBack Directory
[Name]

Macrocarpal C
[CAS]

142628-53-3
[Synonyms]

Macrocarpal C
Macrocarpal C/G
1,3-Benzenedicarboxaldehyde,5-[(1R)-1-[(1aR,4aR,7S,7aR,7bR)-decahydro-1,1,7-trimethyl-4-methylene-1H-cycloprop[e]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxy-
5-[(1R)-1-[(1aR,4aR,7S,7aR,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde
[Molecular Formula]

C28H38O5
[MDL Number]

MFCD17214864
[MOL File]

142628-53-3.mol
[Molecular Weight]

454.6
Chemical PropertiesBack Directory
[Boiling point ]

509.6±50.0 °C(Predicted)
[density ]

1.20±0.1 g/cm3(Predicted)
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

powder
[pka]

5.40±0.50(Predicted)
[color ]

Yellow
Hazard InformationBack Directory
[Description]

Macrocarpal C, isolated from the fresh leaves of Eucalyptus globulus Labill. (Lan An) and identified as its major antifungal component by bioassay-guided purification, the antifungal action of macrocarpal C was associated with increases of membrane permeability, intracellular ROS and DNA fragmentation.
[Uses]

Macrocarpal C can be isolated from the 95 % ethanol extract of fresh leaves of E. globulus. Macrocarpal C inhibits the growth of T. mentagrophytes via an increase in the permeability of the fungal membrane. Macrocarpal C increases the production of intracellular ROS and? induces apoptosis as a consequence of DNA fragmentation[1].
[Definition]

ChEBI: Macrocarpal C is a sesquiterpenoid.
[target]

ROS | Antifection
[References]

[1] Jack Ho Wong, et al. Antifungal mode of action of macrocarpal C extracted from Eucalyptus globulus Labill (Lan An) towards the dermatophyte Trichophyton mentagrophytes. Chin Med. 2015, 10, 34.
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