ZfN: Search Results

Browse byFacets

Bookbag ( 0 )

'Sesquiterpenoids' in keywords

Results 7 Items

1	Author	Wanda Kisiel, Klaudia Michalska	Requires cookie*
	Title	Sesquiterpenoids and Phenolics from Crepis conyzifolia
	Abstract	From the roots of Crepis conyzifolia, two new and two known guaianolides were isolated together with three known phenylpropanoids. Structures of the new compounds were estab lished as 8ß-hydroxy-4ß, 15-dihydrozaluzanin C and 4ß, 15, llß , 13-tetrahydrozaluzanin C-3-O-ß-glucopyranoside by spectral methods. The identity of 8 -epiisolippidiol and dentalactone was also discussed.
	Reference	Z. Naturforsch. 56c, 961—964 (2001); received July 30/August 28 2001
	Published	2001
	Keywords	Crepis conyzifolia, Sesquiterpenoids, Phenolics
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/56/ZNC-2001-56c-0961.pdf
	Identifier	ZNC-2001-56c-0961
	Volume	56

2	Author	A. Stärk, T. Anke, A. Kirfel, G. Will	Requires cookie*
	Title	Lentinellic Acid, a Biologically Active Protoilludane Derivative from Lentinellus Species (Basidiomycetes) [1]
	Abstract	A new antimicrobial and cytotoxic sesquiterpenoid, lentinellic acid (1), has been isolated from submerged cultures of Lentinellus ursinus and L. omphalodes. The structure of the antibiotic was elucidated by spectroscopic methods and a single crystal X-ray analysis. 1 may be formed biogenetically by condensation of a protoilludane aldehyde 4 with a malonate unit.
	Reference	Z. Naturforsch. 43c, 177—183 (1988); received October 16 1987
	Published	1988
	Keywords	Lentinellus, Basidiomycetes, Sesquiterpenoids, Protoilludanes, Lentinellic Acid, Antibiotics
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/43/ZNC-1988-43c-0177.pdf
	Identifier	ZNC-1988-43c-0177
	Volume	43

3	Author	JoH. An, N. Es, D. Asen, Ro Ck, W. Olfgang Steglich	Requires cookie*
	Title	Phellodonic Acid, a New Biologically Active Hirsutane Derivative from Phellodon melaleucus (Thelephoraceae, Basidiomycetes) [1]
	Abstract	A new hirsutane derivative, phellodonic acid (1), has been isolated from fermentations of Phellodon melaleucus strain 87113. Its structure was elucidated by spectroscopic methods. The compound exhibits antibiotic activities towards bacteria and fungi. 1 is the first bioactive metabolite from cultures of a species belonging to the family Thelephoraceae.
	Reference	Z. Naturforsch. 48c, 545—549 (1993); received April 23 1993
	Published	1993
	Keywords	Phellodon melaleucus, Sesquiterpenoids, Hirsutane, Phellodonic Acid, Antibiotic
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/48/ZNC-1993-48c-0545.pdf
	Identifier	ZNC-1993-48c-0545
	Volume	48

4	Author	Z. Naturforsch	Requires cookie*
	Title	Kuehneromycins A and B, Two New Biological Active Compounds from a Tasmanian Kuehneromyces sp. (Strophariaceae, Basidiomycetes)
	Abstract	G erh ard E rk e l3, K irsten L o ren zen 3, Timm A n k ea, R obert V eltenb, A lb erto G im en ezb, and W olfgang Steglichb In a search for new inhibitors of RNA-directed DNA-polymerases kuehneromycin A (1) was isolated from fermentations of a Tasmanian Kuehneromyces species. Its structure was elucidated by spectroscopic methods. Kuehneromycin A (1) is a non-competitive inhibitor of avian myeloblastosis virus (Kj 200 ^i m) and moloney murine leukemia virus (K; 40 (.i m) reverse transcriptases. The second compound, kuehneromycin B (2) is a strong inhibitor of platelet aggregation stimulated with different inducers. In addition, both compounds exhibit cytotoxic and antimicrobial activities.
	Reference	Z. Naturforsch. 50c, 1 (1995); received October 5 1994
	Published	1995
	Keywords	Kuehneromyces sp, Basidiomycetes, Sesquiterpenoids, Drimanes, Nordrimanes
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/50/ZNC-1995-50c-0001.pdf
	Identifier	ZNC-1995-50c-0001
	Volume	50

5	Author	BerndR T Simoneit3, BorysM. Didykb	Requires cookie*
	Title	The Lipid and Resin Composition of Laretia compacta Phil, from the Andes of Chile
	Abstract	The lipid/resin components of Laretia compacta were characterized by GC-MS and CSIA. The lipid components consist of «-alkanes, «-alkanoic acids and «-alkanols all with low car bon number maxima and high CPI values. The resin components are comprised of major amounts of tetracyclic diterpenoids with a minor content of mono-and sesquiterpenoids. The kaurene skeleton predominates with some phyllocladenes. Phytosterols are trace compo nents. The 6 13C data of the individual alkanes in the hydrocarbon fraction place this species in the C4 plant group.
	Reference	Z. Naturforsch. 54c, 309 (1999); received October 7 1998/February 9 1999
	Published	1999
	Keywords	Laretia, Resin, Sesquiterpenoids, Kaurene and Phyllocladene Diterpenoids, Phytosterols
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/54/ZNC-1999-54c-0309.pdf
	Identifier	ZNC-1999-54c-0309
	Volume	54

6	Author	H. Eidrun, A. Nke, E. Lisabeth, H. Illen, -. M. Aske, W. Olfgang Steglich	Requires cookie*
	Title	9 ß-Hydroxymarasmic Acid and Other Sesquiterpenoids from Submerged Cultures of a Basidiomycete [1]
	Abstract	9 ß-Hydroxymarasmic acid, a new sesquiterpenoid, marasmic acid and isovelleral were isolated from cultures of a basidiomycete. Comparison of the antimicrobial activity of the three natural compounds together with two n-butyl ether derivatives of marasmic acid revealed MICs against bacteria in the range of 0 .2 —20 ng/ml. The antifungal, cytotoxic and phytotoxic activities of isovelleral were similar to those exhibited by marasmic acid, whereas the marasmic acid deriva tives were considerably less active than the parent compound. Isovelleral was the only compound to show hemolytic activity.
	Reference	Z. Naturforsch. 44c, 1 (1989); received August 31 1988
	Published	1989
	Keywords	Marasmic Acid, 9 ß-Hydroxymarasmic Acid, Isovelleral, Sesquiterpenoids, Antibiotics, Basidiomycetes
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/44/ZNC-1989-44c-0001.pdf
	Identifier	ZNC-1989-44c-0001
	Volume	44

7	Author	Wolf-Rainer Abraham, Hans-Adolf Arfmanna, Wolfgang Gierschb	Requires cookie*
	Title	Microbial Hydroxylation of Precursors of Sinensal
	Abstract	In order to produce the important flavour com pound sinensal microbial co-hydroxylation o f farnesene and its sulfone derivative were investigated. W hile farnesene proved to be a poor substrate, its sulfone could be hydroxylated to the co-hydroxyfamesene sulfones in up to 27% yield. Some strains could discriminate between the yields products hycroxylated at different positions could also be isolated.
	Reference	Z. Naturforsch. 47c, 851 (1992); received September 15/October 26 1992
	Published	1992
	Keywords	Microbial Hydroxylation, Sesquiterpenoids, Sinensal, Farnesene Sulfone, M onocyclofam esanes
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_C/47/ZNC-1992-47c-0851.pdf
	Identifier	ZNC-1992-47c-0851
	Volume	47