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Five new polar sterols from the black coral Antipathes subpinnata

Aiello, A. ; Fattorusso, E. ; Menna, M.

Amsterdam : Elsevier

Steroids 56 (1991), S. 513-517

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ISSN: 0039-128X

Keywords: (20S)-cholest-4-ene-16β,18,20-triol-3-one ; (20S,22E)-cholesta-1,4,22-triene-18,20-diol-3-one ; (20S,22E)-cholesta-4, 22-diene-16β,18,20-triol-3-one ; Antipathes subpinnata, sterols ; anthozoan ; black coral, sterols ; sterols

Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002

Topics: Medicine

Type of Medium: Electronic Resource

URL: http://linkinghub.elsevier.com/retrieve/pii/0039-128X(91)90116-D

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Isolation of five new 5α-hydroxy-6-keto-Δ^7 sterols from the marine sponge Oscarella lobularis

Aiello, A. ; Fattorusso, E. ; Magno, S. ; [et al.]

Amsterdam : Elsevier

Steroids 56 (1991), S. 337-340

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ISSN: 0039-128X

Keywords: 24-ethylcholest-7-ene-3β,5α-diol-6-one ; 24-methylcholesta-7,22E-diene-3β, 5α-diol-6-one ; 24-methylcholesta-7,24(28)-diene-3β,5α-diol-6-one ; Os-carella lobularis ; cholest-7-ene-3β,5α-diol-6-one ; cholesta-7,22E-diene-3β,5α-diol-6-one ; demospongia ; sterols

Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002

Topics: Medicine

Type of Medium: Electronic Resource

URL: http://linkinghub.elsevier.com/retrieve/pii/0039-128X(91)90057-3

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2-Amino-6-[(1'R,2'S)-1',2'-dihydroxypropyl]-3-methyl-pterin-4-one, a biologically active metabolite from the anthozoanAstroides calycularis Pallas (1987)

Aiello, A. ; Fattorusso, E. ; Magno, S. ; [et al.]

Springer

Cellular and molecular life sciences 43 (1987), S. 950-952

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ISSN: 1420-9071

Keywords: 3-Methyl-L-erythro-biopterin ; 2-amino-6-[(1'R,2'S)-1',2'-dihydroxypropyl]-3-methyl-pterin-4-one ; Astroides calycularis Pallas ; anthozoan

Source: Springer Online Journal Archives 1860-2000

Topics: Biology , Medicine

Notes: Summary 2-Amino-6-[(1'R,2'S)-1',2'-dihydroxypropyl]-3-methyl-pterin-4-one (1) has been isolated from the marine anthozoanAstroides calycularis; its structure was illustrated by spectral analyses including 2D-NMR and by partial synthesis.1 appears to possess cell-growth inhibiting activity.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1007/BF01951683

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