Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Melchor G. Hernández"'
Publikováno v:
Molecules, Vol 17, Iss 2, Pp 1744-1750 (2012)
The biotransformation of 13a,17-dihydroxystemodane (3) with the fungus Cephalosporium aphidicola afforded 13a,17,18-trihydroxystemodane (4), 3b,13a,17-tri-hydroxystemodane (5), 13a,17-dihydroxy-stemodan-18-oic acid (6), 3b,11β,13a,17-tetra-hydroxyst
Externí odkaz:
https://doaj.org/article/d56b7ead89b147e4a796b93ca618c67c
Publikováno v:
Phytochemistry Letters. 50:36-39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::029ce7b908c86c8feab8fb987f42e91a
https://doi.org/10.1016/j.phytol.2022.05.003
https://doi.org/10.1016/j.phytol.2022.05.003
Publikováno v:
Molecules
Molecules; Volume 17; Issue 2; Pages: 1744-1750
Digital.CSIC. Repositorio Institucional del CSIC
instname
Molecules, Vol 17, Iss 2, Pp 1744-1750 (2012)
Molecules; Volume 17; Issue 2; Pages: 1744-1750
Digital.CSIC. Repositorio Institucional del CSIC
instname
Molecules, Vol 17, Iss 2, Pp 1744-1750 (2012)
The biotransformation of 13a,17-dihydroxystemodane (3) with the fungus Cephalosporium aphidicola afforded 13a,17,18-trihydroxystemodane (4), 3b,13a,17-tri-hydroxystemodane (5), 13a,17-dihydroxy-stemodan-18-oic acid (6), 3b,11β,13a,17-tetra-hydroxyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f092fbe058a6f52207231f36e6c3c42b
http://europepmc.org/articles/PMC6268689
http://europepmc.org/articles/PMC6268689
Publikováno v:
Phytochemistry. 70:1038-1048
Nine taxa of the Sideritis genus, Sideritis argosphacelus var. spicata, Sideritis candicans var. eriocephala,Sideritis discolor, Sideritis kuegleriana, Sideritis lotsyi, Sideritis lotsyi var. mascaensis, Sideritis marmorea, Sideritis soluta and Sider
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f18cf3915b94d344bb3845c9277f35e9
https://doi.org/10.1016/j.phytochem.2009.05.011
https://doi.org/10.1016/j.phytochem.2009.05.011
Publikováno v:
Journal of Natural Products. 72:87-91
The incubation of 19-hydroxy-13-epi-ent-pimara-9(11),15-diene (4) with Gibberella fujikuroi gave 8 alpha,19-dihydroxy-9 alpha,11alpha-epoxy-13-epi-ent-pimara-15-ene (6), 7-oxo-11 alpha,19-dihydroxy-13-epi-ent-pimara-8(9),15-diene (7), 7-oxo-11beta,19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33a99f2da023a6060e636fc8961cfad6
https://doi.org/10.1021/np800647v
https://doi.org/10.1021/np800647v
Publikováno v:
Tetrahedron. 61:5623-5632
The microbiological transformation of 7-oxo- ent -kaur-16-ene by the fungus Gibberella fujikuroi gave fujenoic acid as the main compound, whilst the incubation of 18-hydroxy-7-oxo- ent -kaur-16-ene and 3α,18-dihydroxy-7-oxo- ent -kaur-16-ene afforde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3518c61ee1deaf97e7d458f0a235907d
https://doi.org/10.1016/j.tet.2005.03.089
https://doi.org/10.1016/j.tet.2005.03.089
Publikováno v:
Tetrahedron. 60:7921-7932
The microbiological transformation of 13α,17-dihydroxy-stemodane (2) by the fungus Mucor plumbeus afforded 13α,17,19-trihydroxy-stemodane (3), 3β,13α,17-trihydroxy-stemodane (5), 3-oxo-13α,17-dihydroxy-stemodane (7), 7α,13α,17,19-tetrahydroxy-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15d9b37d5a7992d8c607bb4977a2708d
https://doi.org/10.1016/j.tet.2004.06.055
https://doi.org/10.1016/j.tet.2004.06.055
The Microbiological Transformation of Two 15β-Hydroxy-ent-kaurene Diterpenes by Gibberella fujikuroi
Publikováno v:
Journal of Natural Products. 67:64-69
The incubation of 15‚-hydroxy-3-oxo-ent-kaur-16-ene (1) with the fungus Gibberella fujikuroi afforded 11‚-hydroxy-3,15-dioxo-ent-kaurane (6), 11‚,15‚-dihydroxy-3-oxo-ent-kaur-16-ene (8), 7‚,11‚,15‚-trihydroxy-3-oxo-ent-kaur-16-ene (9),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062c834e6734904d69c4fb14f2e8190b
https://doi.org/10.1021/np030363n
https://doi.org/10.1021/np030363n
Publikováno v:
Natural Product Research. 17:141-144
The structure of a diterpene, which has been isolated form Sideritis athoa , has been corrected from 3 g ,18-dihydroxy- ent -kaur-16-ene to 1 f ,18-dihydroxy- ent -kaur-16-ene (canadiol).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7373e93ff6334cfcec7857685c40971
https://doi.org/10.1080/1478641031000103722
https://doi.org/10.1080/1478641031000103722
Publikováno v:
Pure and Applied Chemistry. 73:579-582
One of our research lines has been the chemical studies among Calceolaria species (Scrophulariaceae), from which have been isolated 77 new diterpenes of various skeleton types (labdanes, pimaranes, stemaranes, and stemodanes), all coming from a commo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b01cf122aebe94a165d62b3d2d21a2c
https://doi.org/10.1351/pac200173030579
https://doi.org/10.1351/pac200173030579