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Macrocarpal D

Names

[ CAS No. ]:
142647-71-0

[ Name ]:
Macrocarpal D

[Synonym ]:
2,4,6-Trihydroxy-5-{1-[7-(2-hydroxy-2-propanyl)-1,4-dimethyl-1,2,3,3a,4,5,6,7-octahydro-1-azulenyl]-3-methylbutyl}isophthalaldehyde
1,3-Benzenedicarboxaldehyde, 2,4,6-trihydroxy-5-[(1R)-3-methyl-1-[(1R,3aR,4R,7R)-1,2,3,3a,4,5,6,7-octahydro-7-(1-hydroxy-1-methylethyl)-1,4-dimethyl-1-azulenyl]butyl]-
2,4,6-Trihydroxy-5-{(1R)-1-[(1R,3aR,4R,7R)-7-(2-hydroxy-2-propanyl)-1,4-dimethyl-1,2,3,3a,4,5,6,7-octahydro-1-azulenyl]-3-methylbutyl}isophthalaldehyde
2,4,6-trihydroxy-5-{1-[5-(1-hydroxy-isopropyl)-2,8-dimethylbicyclo[5.3.0]dec-6-en-8-yl]-3-methylbutyl}benzene-1,3-dicarbaldehyde
1,3-Benzenedicarboxaldehyde, 2,4,6-trihydroxy-5-[3-methyl-1-[1,2,3,3a,4,5,6,7-octahydro-7-(1-hydroxy-1-methylethyl)-1,4-dimethyl-1-azulenyl]butyl]-
Macrocarpal D
2,4,6-trihydroxy-5-(1-(5-(1-hydroxy-isopropyl)-2,8-dimethylbicyclo(5.3.0)dec-6-en-8-yl)-3-methylbutyl)benzene-1,3-dicarbaldehyde

Biological Activity

[Description]:

Macrocarpal D is a potent antibacterial agent. Macrocarpal D is a phloroglucinol dialdehyde diterpene derivatives that can be found in the leaves of Eucalyptus macrocarpa[1].

[Related Catalog]:

Research Areas >> Infection
Signaling Pathways >> Anti-infection >> Bacterial

[In Vitro]

Macrocarpal D 显示抗菌活性，对 Staphylococcus aureus FAD209P, Micrococcus luteus ATCC9341, Bacillus subtiUs PCI2l9, Mycobacterium smegmatis ATCC607 的 MIC 值分别为 1.56, 1.56, 0.78, 1.56 µg/mL[1]。

[References]

[1]. Yamakoshi Y, et al. Isolation and characterization of macrocarpals B--G antibacterial compounds from Eucalyptus macrocarpa. Biosci Biotechnol Biochem. 1992 Oct;56(10):1570-6.  

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
553.3±50.0 °C at 760 mmHg

[ Molecular Formula ]:
C28H40O6

[ Molecular Weight ]:
472.614

[ Flash Point ]:
302.5±26.6 °C

[ Exact Mass ]:
472.282501

[ PSA ]:
115.06000

[ LogP ]:
9.19

[ Vapour Pressure ]:
0.0±1.6 mmHg at 25°C

[ Index of Refraction ]:
1.588

Safety Information

[ Hazard Codes ]:
Xi

Related Compounds