-
1
-
-
0034911075
-
Multiplolides A and B, new antifungal 10-membered lactones from Xylaria multiplex
-
S. Boonphong, P. Kittakoop, M. Isaka, D. Pittayakhajonwut, M. Tanticharoen, and Y. Thebtaranonth Multiplolides A and B, new antifungal 10-membered lactones from Xylaria multiplex J. Nat. Prod. 64 2001 965 967
-
(2001)
J. Nat. Prod.
, vol.64
, pp. 965-967
-
-
Boonphong, S.1
Kittakoop, P.2
Isaka, M.3
Pittayakhajonwut, D.4
Tanticharoen, M.5
Thebtaranonth, Y.6
-
2
-
-
0026046311
-
Isolation and structure elucidation of hymatoxins B-E and other phytotoxins from Hypoxylon mammatum fungal pathogen of Leuce poplars
-
K. Borgschulte, S. Rebuffat, W. Trowitzsch-Kienast, D. Schomburg, J. Pinon, and B. Bodo Isolation and structure elucidation of hymatoxins B-E and other phytotoxins from Hypoxylon mammatum fungal pathogen of Leuce poplars Tetrahedron 47 1991 8351 8360
-
(1991)
Tetrahedron
, vol.47
, pp. 8351-8360
-
-
Borgschulte, K.1
Rebuffat, S.2
Trowitzsch-Kienast, W.3
Schomburg, D.4
Pinon, J.5
Bodo, B.6
-
3
-
-
34247154840
-
Kolokosides A-D: Triterpenoid glycosides from a Hawaiian isolate of Xylaria sp
-
S.T. Deyrup, J.B. Gloer, K. O'Donnell, and D.T. Wicklow Kolokosides A-D: triterpenoid glycosides from a Hawaiian isolate of Xylaria sp. J. Nat. Prod. 70 2007 378 382
-
(2007)
J. Nat. Prod.
, vol.70
, pp. 378-382
-
-
Deyrup, S.T.1
Gloer, J.B.2
O'Donnell, K.3
Wicklow, D.T.4
-
4
-
-
77957880328
-
Eremophilane sesquiterpenes from the endophyte Microdiplodia sp. KS 75-1 and revision of the stereochemistries of phomadecalins C and D
-
T. Hatakeyama, T. Koseki, T. Murayama, and Y. Shiono Eremophilane sesquiterpenes from the endophyte Microdiplodia sp. KS 75-1 and revision of the stereochemistries of phomadecalins C and D Phytochem. Lett. 3 2010 148 151
-
(2010)
Phytochem. Lett.
, vol.3
, pp. 148-151
-
-
Hatakeyama, T.1
Koseki, T.2
Murayama, T.3
Shiono, Y.4
-
5
-
-
77951523583
-
Eremophilane-type sesquiterpenes from the fungus Xylaria sp. BCC 21097
-
M. Isaka, P. Chinthanom, T. Boonruangprapa, N. Rungjindamai, and U. Pinruan Eremophilane-type sesquiterpenes from the fungus Xylaria sp. BCC 21097 J. Nat. Prod. 73 2010 683 687
-
(2010)
J. Nat. Prod.
, vol.73
, pp. 683-687
-
-
Isaka, M.1
Chinthanom, P.2
Boonruangprapa, T.3
Rungjindamai, N.4
Pinruan, U.5
-
6
-
-
79952287012
-
Ring B aromatic norpimarane glucoside from a Xylaria sp
-
M. Isaka, A. Yangchum, P. Auncharoen, K. Srichomthong, and P. Srikitikulchai Ring B aromatic norpimarane glucoside from a Xylaria sp. J. Nat. Prod. 74 2011 300 302
-
(2011)
J. Nat. Prod.
, vol.74
, pp. 300-302
-
-
Isaka, M.1
Yangchum, A.2
Auncharoen, P.3
Srichomthong, K.4
Srikitikulchai, P.5
-
7
-
-
0028930595
-
Hymatoxins K and L, novel phytotoxins from Hypoxylon mammatum, fungal pathogen of aspens
-
A. Jossang, B. Mbeminack, J. Pinon, and B. Bodo Hymatoxins K and L, novel phytotoxins from Hypoxylon mammatum, fungal pathogen of aspens Nat. Prod. Lett. 6 1995 37 42
-
(1995)
Nat. Prod. Lett.
, vol.6
, pp. 37-42
-
-
Jossang, A.1
Mbeminack, B.2
Pinon, J.3
Bodo, B.4
-
8
-
-
0035929454
-
Five unique compounds: Xyloketals from mangrove fungus Xylaria sp. from the South China Sea coast
-
Y. Lin, X. Wu, S. Feng, G. Jiang, J. Luo, S. Zhou, L.L.P. Vrijmoed, E.B.G. Jones, K. Krohn, K. Steingröver, and F. Zsila Five unique compounds: xyloketals from mangrove fungus Xylaria sp. from the South China Sea coast J. Org. Chem. 66 2001 6252 6256
-
(2001)
J. Org. Chem.
, vol.66
, pp. 6252-6256
-
-
Lin, Y.1
Wu, X.2
Feng, S.3
Jiang, G.4
Luo, J.5
Zhou, S.6
Vrijmoed, L.L.P.7
Jones, E.B.G.8
Krohn, K.9
Steingröver, K.10
Zsila, F.11
-
9
-
-
0035862615
-
A novel N-cinnamoylcyclopeptide containing an allenic ether from the fungus Xylaria sp. (strain #2508) from the South China Sea
-
Y. Lin, X. Wu, S. Feng, G. Jiang, S. Zhou, L.L.P. Vrijmoed, and E.B.G. Jones A novel N-cinnamoylcyclopeptide containing an allenic ether from the fungus Xylaria sp. (strain #2508) from the South China Sea Tetrahedron Lett. 42 2001 449 451
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 449-451
-
-
Lin, Y.1
Wu, X.2
Feng, S.3
Jiang, G.4
Zhou, S.5
Vrijmoed, L.L.P.6
Jones, E.B.G.7
-
10
-
-
2142858450
-
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
-
I. Ohtani, T. Kusumi, Y. Kashman, and H. Kakisawa High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids J. Am. Chem. Soc. 113 1991 4092 4096
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 4092-4096
-
-
Ohtani, I.1
Kusumi, T.2
Kashman, Y.3
Kakisawa, H.4
-
11
-
-
0033544770
-
Structure and absolute stereochemistry of HIV-1 integrase inhibitor integric acid. A novel eremophilane sesquiterpenoid produced by a Xylaria sp
-
S.B. Singh, D. Zink, J. Polishook, D. Valentino, A. Shafiee, K. Silverman, P. Felock, A. Teran, D. Vilella, D.J. Hazuda, and R.B. Lingham Structure and absolute stereochemistry of HIV-1 integrase inhibitor integric acid. A novel eremophilane sesquiterpenoid produced by a Xylaria sp. Tetrahedron Lett. 40 1999 8775 8779
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 8775-8779
-
-
Singh, S.B.1
Zink, D.2
Polishook, J.3
Valentino, D.4
Shafiee, A.5
Silverman, K.6
Felock, P.7
Teran, A.8
Vilella, D.9
Hazuda, D.J.10
Lingham, R.B.11
-
12
-
-
0037067341
-
Novel sesquiterpenoids from the fermentation of Xylaria persicaria are selective ligands for the NPY Y5 receptor
-
C.J. Smith, N.R. Morin, G.F. Bills, A.W. Dombrowski, G.M. Salituro, S.K. Smith, A. Zhao, and D.J. MacNeil Novel sesquiterpenoids from the fermentation of Xylaria persicaria are selective ligands for the NPY Y5 receptor J. Org. Chem. 67 2002 5001 5004
-
(2002)
J. Org. Chem.
, vol.67
, pp. 5001-5004
-
-
Smith, C.J.1
Morin, N.R.2
Bills, G.F.3
Dombrowski, A.W.4
Salituro, G.M.5
Smith, S.K.6
Zhao, A.7
MacNeil, D.J.8
-
13
-
-
19644377388
-
Xylactam, a new nitrogen-containing compound from the fruiting bodies of Ascomycete Xylaria euglossa
-
X.-N. Wang, R.-X. Tan, and J.-K. Liu Xylactam, a new nitrogen-containing compound from the fruiting bodies of Ascomycete Xylaria euglossa J. Antibiot. 58 2005 268 270
-
(2005)
J. Antibiot.
, vol.58
, pp. 268-270
-
-
Wang, X.-N.1
Tan, R.-X.2
Liu, J.-K.3
|