macrocarpal C

Modify Date: 2024-01-19 18:09:12

macrocarpal C structure	Common Name	macrocarpal C
	CAS Number	142628-53-3	Molecular Weight	454.60
	Density	1.2±0.1 g/cm3	Boiling Point	503.9±50.0 °C at 760 mmHg
	Molecular Formula	C₂₈H₃₈O₅	Melting Point	N/A
	MSDS	N/A	Flash Point	272.6±26.6 °C

Use of macrocarpal C

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
Synonym	More Synonyms

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	Research Areas >> Others Signaling Pathways >> Anti-infection >> Fungal
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

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