• 제목/요약/키워드: sponge Phorbas sp.

검색결과 3건 처리시간 0.017초

A New Sponge of the Genus Phorbas (Poecilosclerida: Hymedesmiidae) from Gageodo Island (So-Huksando), Korea

  • Sim, Chung-Ja;Kim, Hyung-June
    • Animal cells and systems
    • /
    • 제8권3호
    • /
    • pp.135-137
    • /
    • 2004
  • A taxonomic study on marine sponges was conducted with materials collected from Gageodo Island, Korea, from August 1999 to July 2001 by SCUBA diving. Among them, Phorbas gukhulensis n. sp. is new to science. Phorbas gukhulensis n. sp. is similar to P. fitictius Pulitzer-Finali from which it differs in spicule size and growth form.

A new derivative of phorbaketals isolated from a Marine Sponge Phorbas species

  • Hwang, Buyng-Su;Yang, Cao;Rho, Jung-Rae
    • 한국자기공명학회논문지
    • /
    • 제15권2호
    • /
    • pp.128-136
    • /
    • 2011
  • A new sesterterpenoid, phorbaketal derivative, was isolated from the marine sponge Phorbas species. Its planar structures was completely determined from a combination of extensive 1D and 2D NMR experiments and MS data, and also the stereochemistry on the chiral centers were established by the ROESY experiment and the comparison with the $^1H$ and $^{13}C$ chemical shifts of the known phorbaketal compounds. This compound 1 moderately showed cytotoxicity effect against hepatoma cancer HepG2 cell.

Structure determination of two new compounds isolated from a marine sponge Haliclona(Gellius) sp.

  • Lee, Kyung;Kim, Yun Na;Jeong, Eun Ju
    • 한국자기공명학회논문지
    • /
    • 제25권2호
    • /
    • pp.24-32
    • /
    • 2021
  • Two new sesterterpenes, including a known sesterterpene, were isolated from the marine sponge Haliclona sp. collected in the Gageo island, Korea. One of the new sesterterpenes (1) was an unusual compound possessing a spiroketal moiety and the other (2) represented a four ring-fused skeleton. The planar structure of compound 1 was identical to gombaspiroketals A and B isolated from the marine sponge Clathria gombawuiensis, but the configuration for the two chiral centers was different each other. On the other hand, the skeletal structure of compound 2 was similar to that of phorone A isolated from Phorbas sp. and a compound from C. gombawuiensis, except for one configuration at C-8. However, in comparing the 1H and 13C NMR spectral data, the proton and carbon chemical shifts for the three compounds were almost consistent. The NOESY spectrum revealed that the C-8 configuration of 2 was reversed to that of the two reported compounds. The configuration for compound 2 was supported by quantum mechanical calculation for the carbon chemical shifts and DP4+ probability for the protons and carbons of 2.