Zobrazeno 1 - 10
of 182
pro vyhledávání: '"Stephen M. Parrish"'
Autor:
Miles, Josephine
Publikováno v:
Victorian Studies, 1965 Mar 01. 8(3), 290-292.
Externí odkaz:
https://www.jstor.org/stable/3825577
Autor:
George H. Klumpner
Publikováno v:
The Psychoanalytic Quarterly. 50:96-134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3b3d114416ed4cdabb77b913abbe423
https://doi.org/10.1080/21674086.1981.11926946
https://doi.org/10.1080/21674086.1981.11926946
Autor:
Ram P. Neupane, Stephen M. Parrish, Jayanti Bhandari Neupane, Wesley Y. Yoshida, M. L. Richard Yip, James Turkson, Mary Kay Harper, John D. Head, Philip G. Williams
Publikováno v:
Marine Drugs, Vol 17, Iss 7, p 423 (2019)
Several known sesquiterpenoid quinones and quinols (1−9), and kauamide (10), a new polyketide-peptide containing an 11-membered heterocycle, were isolated from the extracts of the Hawaiian marine sponge Dactylospongia elegans. The planar structure
Externí odkaz:
https://doaj.org/article/3646b2d437074b46856998ae2f37a10e
Publikováno v:
J Nat Prod
Four compounds (1–4) were isolated from a Hawaiian sponge of the genus Myrmekioderma. Myrmenaphthol A (1) incorporates two unusual elements into an oxidized steroidal core: a naphthyl AB-ring system and a hydroxy group at C-2. A comparison of the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d5bb5d87a7f37398bd6966c22b3aba
https://doi.org/10.1021/acs.jnatprod.9b00665
https://doi.org/10.1021/acs.jnatprod.9b00665
Autor:
James Turkson, Philip G. Williams, M.L. Richard Yip, Wesley Y. Yoshida, John D. Head, Ram P. Neupane, Stephen M. Parrish
Publikováno v:
Planta Medica. 81:S1-S381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14d21f67d0ea51e66cd671abaf21c671
https://doi.org/10.1055/s-0036-1596653
https://doi.org/10.1055/s-0036-1596653
Publikováno v:
Journal of natural products. 80(3)
Three new ulapualides (3-5) were isolated from egg masses of the nudibranch Hexabranchus sanguineus. The structures of 3-5 were deduced by analyses of physical and spectroscopic data in comparisons with ulapualides A (1) and B (2). Ulapualide C demon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae9e6bf9084316797e143301eaeda2d5
https://pubmed.ncbi.nlm.nih.gov/28098996
https://pubmed.ncbi.nlm.nih.gov/28098996
Autor:
Stephen M. Parrish, Eun-Jung Park, Tamara P. Kondratyuk, Philip G. Williams, John M. Pezzuto, Wesley Y. Yoshida, Michelle Kelly
Publikováno v:
Journal of Natural Products
New compounds 18-nor-3,17-dihydroxyspongia-3,13(16),14-trien-2-one (1), 18-nor-3,5,17-trihydroxyspongia-3,13(16),14-trien-2-one (2), and spongiapyridine (3) and the known compound 17-hydroxy-4-epi-spongialactone A (4) were isolated from an Indonesian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b71f31e9aa50cf67653f385b7957337
https://doi.org/10.1021/np500256w
https://doi.org/10.1021/np500256w
Autor:
Jingqiu Dai, Philip G. Williams, M.L. Richard Yip, Michelle Kelly, Stephen M. Parrish, James Turkson, Wesley Y. Yoshida
Publikováno v:
ChemInform. 47
isolation and structure elucidation of purpuramine M (Ia) and purpuramine N (Ib), araplysillin VII (IIa), araplysillin VIII (IIb), araplysillin IX (III), araplysillin X (IVa), and araplysillin XI (IVb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2eb1b2c59b6e8683e165aea9bb8095c
https://doi.org/10.1002/chin.201619186
https://doi.org/10.1002/chin.201619186
Publikováno v:
Planta Medica. 78:1357-1362
Examination of an active extract of the fruit of Ficus benjamina var. nuda (Miq.) Barrett (Moraceae) has led to the isolation of six new isoflavones and two coumarano-chroman-4-one, along with fifteen known compounds. The structures of the eight new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c55cfc9b41a30c2c9e2b16ddb7f3d121
https://doi.org/10.1055/s-0032-1315001
https://doi.org/10.1055/s-0032-1315001
Autor:
Stephen M. Parrish, Brent K. Rubio, Peter J. Schupp, Tom Schils, Wesley Y. Yoshida, Philip G. Williams
Publikováno v:
Tetrahedron Letters. 51:6718-6721
Bouillomides A (1) and B (2) are two depsipeptide analogues of dolastatin 13. Isolated from a Guamanian sample of Lyngbya bouillonii, the planar structures were elucidated on the basis of HR-ESI-MS and NMR data, while the absolute configurations were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::040612c60f5ca824ed16f4b4a29a827e
https://doi.org/10.1016/j.tetlet.2010.10.062
https://doi.org/10.1016/j.tetlet.2010.10.062