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Chemical Compound Review

Lanostane     4,4,10,13,14-pentamethyl-17- (6...

Synonyms: AC1L2RDB, AR-1J2989, AC1Q1IY0, 474-20-4
 
 
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High impact information on Lanostane

  • A new lanostane-type terpenoid, lucidenic acid SP1 (1), was isolated from a CHCl(3)-soluble fraction of Ganoderma lucidum spores together with four other known compounds (2 - 5) [1].
  • Neokadsuranic acid A, which is the first triterpenoid with the 14(13-->12) ABEO lanostane skeleton, was isolated from KADSURA HETEROCLITA together with (24 Z)-3-oxo-lanosta-8,24-dien-26-oic acid [2].
  • Marianine, the new lanostane triterpene (1) and marianosides A (2) and B (3) have been isolated from the whole plant of Silybum marianum [3].
  • Ganoderic acid T (GA-T), which is a lanostane triterpenoid purified from methanol extract of G. lucidum mycelia, was found to exert cytotoxicity on various human carcinoma cell lines in a dose-dependent manner, while it was less toxic to normal human cell lines [4].
  • Lanostane triterpenoids and triterpene glycosides from the fruit body of Fomitopsis pinicola and their inhibitory activity against COX-1 and COX-2 [5].
 

Associations of Lanostane with other chemical compounds

  • A new lanostane-type triterpene acid, (20xi)-3-oxolanosta-7,9(11),24-trien-21-oic acid (1; dehydrotrametenonic acid), along with a known triterpene acid, dehydroeburiconic acid (2), were isolated from the epidermis of the sclerotia of Poria cocos [6].
 

Gene context of Lanostane

 

Analytical, diagnostic and therapeutic context of Lanostane

  • Using high performance liquid chromatography, we identified two lanostane-type compounds, i.e. dehydrosulfurenic acid and 15alpha-acetyl-dehydrosulfurenic acid, which could be involved in the anti-inflammatory actions of these extracts [8].
  • The circular dichroism (CD) of the in situ-formed Rh2(OCOCF3)4 complexes of sterically hindered, secondary lanostane alcohols was investigated [9].
  • It was proved by HPLC and TLC investigations, that the crust on top of the fruiting bodies of F. pinicola consists of lanostane derivatives [10].

References

  1. Anticomplement activity of terpenoids from the spores of Ganoderma lucidum. Min, B.S., Gao, J.J., Hattori, M., Lee, H.K., Kim, Y.H. Planta Med. (2001) [Pubmed]
  2. Isolation and Structure Elucidation of Neokadsuranic Acid A, the First Triterpenoid with the 14 (13-->12) abeo Lanostane Skeleton, and (24Z)-3-Oxo-lanosta-8,24-dien-26-oic Acid1. Kangouri, K., Miyoshi, T., Kawashima, A., Ikeda, A., Mizutani, T., Omura, S., Lian-Niang, L., Hong, X. Planta Med. (1989) [Pubmed]
  3. Chymotrypsin inhibitory triterpenoids from Silybum marianum. Ahmed, E., Malik, A., Ferheen, S., Afza, N., Azhar-Ul-Haq, n.u.l.l., Lodhi, M.A., Choudhary, M.I. Chem. Pharm. Bull. (2006) [Pubmed]
  4. Ganoderic acid T from Ganoderma lucidum mycelia induces mitochondria mediated apoptosis in lung cancer cells. Tang, W., Liu, J.W., Zhao, W.M., Wei, D.Z., Zhong, J.J. Life Sci. (2006) [Pubmed]
  5. Lanostane triterpenoids and triterpene glycosides from the fruit body of Fomitopsis pinicola and their inhibitory activity against COX-1 and COX-2. Yoshikawa, K., Inoue, M., Matsumoto, Y., Sakakibara, C., Miyataka, H., Matsumoto, H., Arihara, S. J. Nat. Prod. (2005) [Pubmed]
  6. Dehydrotrametenonic acid and dehydroeburiconic acid from Poria cocos and their inhibitory effects on eukaryotic DNA polymerase alpha and beta. Akihisa, T., Mizushina, Y., Ukiya, M., Oshikubo, M., Kondo, S., Kimura, Y., Suzuki, T., Tai, T. Biosci. Biotechnol. Biochem. (2004) [Pubmed]
  7. Synthetic lanostane-type triterpenoids as inhibitors of DNA topoisomerase II. Wada, S., Tanaka, R. Bioorg. Med. Chem. Lett. (2005) [Pubmed]
  8. Anti-inflammatory activity of the extracts from mycelia of Antrodia camphorata cultured with water-soluble fractions from five different Cinnamomum species. Shen, Y.C., Chou, C.J., Wang, Y.H., Chen, C.F., Chou, Y.C., Lu, M.K. FEMS Microbiol. Lett. (2004) [Pubmed]
  9. Chiroptical properties of binuclear rhodium complexes of lanostane alcohols. Frelek, J., Jagodziński, J., Meyer-Figge, H., Sheldrick, W.S., Wieteska, E., Szczepek, W.J. Chirality. (2001) [Pubmed]
  10. Constituents of various wood-rotting basidiomycetes. Rösecke, J., König, W.A. Phytochemistry (2000) [Pubmed]
 
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