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142628-53-3

142628-53-3 structure
142628-53-3 structure
  • Name: macrocarpal C
  • Chemical Name: 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
  • CAS Number: 142628-53-3
  • Molecular Formula: C28H38O5
  • Molecular Weight: 454.60
  • Catalog: Natural product Sesquiter
  • Create Date: 2017-07-30 09:16:13
  • Modify Date: 2024-01-19 18:09:12
  • 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].

Name 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
Synonyms 2,4,6-Trihydroxy-5-{3-methyl-1-[(1aS,4aR,7R,7aS,7bS)-1a,7,7b-trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulen-7-yl]butyl}isophthalaldehyde
1,3-Benzenedicarboxaldehyde, 5-[1-[(1aS,4aR,7R,7aS,7bS)-decahydro-1a,7,7b-trimethyl-4-methylene-1H-cycloprop[e]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxy-
2,4,6-Trihydroxy-5-{(1R)-3-methyl-1-[(1aR,4aR,7S,7aR,7bR)-1,1,7-trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulen-7-yl]butyl}isophthalaldehyde
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-
macrocarpal-C
macrocarpal G
macrocarpal C
Description 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].
Related Catalog
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.

Density 1.2±0.1 g/cm3
Boiling Point 503.9±50.0 °C at 760 mmHg
Molecular Formula C28H38O5
Molecular Weight 454.60
Flash Point 272.6±26.6 °C
Exact Mass 454.271912
PSA 94.83000
LogP 10.79
Vapour Pressure 0.0±1.3 mmHg at 25°C
Index of Refraction 1.594
Hazard Codes Xi
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