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Items: 1 to 20 of 99

1.

Dereplication of macrocyclic trichothecenes from extracts of filamentous fungi through UV and NMR profiles.

Sy-Cordero AA, Graf TN, Wani MC, Kroll DJ, Pearce CJ, Oberlies NH.

J Antibiot (Tokyo). 2010 Sep;63(9):539-44. doi: 10.1038/ja.2010.77. Epub 2010 Jul 21.

2.

14'-Hydroxymytoxin B and 16-hydroxyroridin E, two new cytotoxic trichothecenes from Myrothecium roridum.

Alvi KA, Rabenstein J, Woodard J, Baker DD, Bergthold JD, Lynch J, Lieu KL, Braude IA.

J Nat Prod. 2002 May;65(5):742-4.

PMID:
12027756
3.

Four new macrocyclic trichothecenes from two strains of marine-derived fungi of the genus Myrothecium.

Xu J, Takasaki A, Kobayashi H, Oda T, Yamada J, Mangindaan RE, Ukai K, Nagai H, Namikoshi M.

J Antibiot (Tokyo). 2006 Aug;59(8):451-5.

PMID:
17080680
4.

Cyclodepsipeptides, sesquiterpenoids, and other cytotoxic metabolites from the filamentous fungus Trichothecium sp. (MSX 51320).

Sy-Cordero AA, Graf TN, Adcock AF, Kroll DJ, Shen Q, Swanson SM, Wani MC, Pearce CJ, Oberlies NH.

J Nat Prod. 2011 Oct 28;74(10):2137-42. doi: 10.1021/np2004243. Epub 2011 Oct 6. Erratum in: J Nat Prod. 2012 Feb 24;75(2):307.

5.

A new macrocyclic trichothecene, 12,13-deoxyroridin E, produced by the marine-derived fungus Myrothecium roridum collected in Palau.

Namikoshi M, Akano K, Meguro S, Kasuga I, Mine Y, Takahashi T, Kobayashi H.

J Nat Prod. 2001 Mar;64(3):396-8.

PMID:
11277768
6.

Harzianums A and B produced by a fungal strain, Hypocrea sp. F000527, and their cytotoxicity against tumor cell lines.

Jin HZ, Lee JH, Zhang WD, Lee HB, Hong YS, Kim YH, Lee JJ.

J Asian Nat Prod Res. 2007 Apr-Aug;9(3-5):203-7.

PMID:
17566911
7.

Macrocyclic trichothecenes as antifungal and anticancer compounds.

de Carvalho MP, Weich H, Abraham WR.

Curr Med Chem. 2016;23(1):23-35. Review.

PMID:
26572613
8.

High-resolution MS, MS/MS, and UV database of fungal secondary metabolites as a dereplication protocol for bioactive natural products.

El-Elimat T, Figueroa M, Ehrmann BM, Cech NB, Pearce CJ, Oberlies NH.

J Nat Prod. 2013 Sep 27;76(9):1709-16. doi: 10.1021/np4004307. Epub 2013 Aug 16.

9.

Cytotoxic trichothecene macrolides from the endophyte fungus Myrothecium roridum.

Liu HX, Liu WZ, Chen YC, Sun ZH, Tan YZ, Li HH, Zhang WM.

J Asian Nat Prod Res. 2016 Jul;18(7):684-9. doi: 10.1080/10286020.2015.1134505. Epub 2016 Jan 21.

PMID:
26795403
10.

Haliclonin A, a new macrocyclic diamide from the sponge Haliclona sp.

Jang KH, Kang GW, Jeon JE, Lim C, Lee HS, Sim CJ, Oh KB, Shin J.

Org Lett. 2009 Apr 16;11(8):1713-6. doi: 10.1021/ol900282m.

PMID:
19296646
11.

A new trichothecene from Myrothecium roridum QDFE005, a symbiotic fungus isolated from Mactra chinensis.

Piao MZ, Shen L, Wang FW.

J Asian Nat Prod Res. 2013;15(12):1284-9. doi: 10.1080/10286020.2013.841141. Epub 2013 Oct 24.

PMID:
24152038
12.

Cytotoxic macrocyclic trichothecenes from the mycelia of Calcarisporium arbuscula Preuss.

Yu NJ, Guo SX, Lu HY.

J Asian Nat Prod Res. 2002 Sep;4(3):179-83.

PMID:
12118505
13.

Structure determination of two new trichothecenes from a halotolerant fungus Myrothecium sp. GS-17 by NMR spectroscopy.

Zhang SY, Li ZL, Guan LP, Wu X, Pan HQ, Bai J, Hua HM.

Magn Reson Chem. 2012 Sep;50(9):632-6. doi: 10.1002/mrc.3845. Epub 2012 Jul 16.

PMID:
22806769
14.

Biologically active metabolites from fungi, 17. 8-alpha-acetoxyverrol, a new member of the trichothecene sesquiterpenes.

Krohn K, Steingröver K, Aust HJ, Draeger S, Schulz B.

Nat Prod Res. 2003 Jan;17(1):67-70.

PMID:
12674145
15.

Two new trichothecenes from Fusarium sporotrichioides.

Bekele E, Rottinghaus AA, Rottinghaus GE, Casper HH, Fort DM, Barnes CL, Tempesta MS.

J Nat Prod. 1991 Sep-Oct;54(5):1303-8.

PMID:
1800633
16.

Cytotoxic macrocyclic diterpenoids from Euphorbia helioscopia.

Tao HW, Hao XJ, Liu PP, Zhu WM.

Arch Pharm Res. 2008 Dec;31(12):1547-51. doi: 10.1007/s12272-001-2149-3. Epub 2008 Dec 20.

PMID:
19099222
17.

Macrocyclic Trichothecenes from Myrothecium roridum Strain M10 with Motility Inhibitory and Zoosporicidal Activities against Phytophthora nicotianae.

Mondol MA, Surovy MZ, Islam MT, Schüffler A, Laatsch H.

J Agric Food Chem. 2015 Oct 14;63(40):8777-86. doi: 10.1021/acs.jafc.5b02366. Epub 2015 Sep 29.

PMID:
26320597
18.

Stereochemistry of the roridins. Diastereomers of roridin E.

Jarvis BB, Wang S.

J Nat Prod. 1999 Sep;62(9):1284-9.

PMID:
10514314
19.

Cytotoxic xanthone-anthraquinone heterodimers from an unidentified fungus of the order Hypocreales (MSX 17022).

Ayers S, Graf TN, Adcock AF, Kroll DJ, Shen Q, Swanson SM, Matthew S, Carcache de Blanco EJ, Wani MC, Darveaux BA, Pearce CJ, Oberlies NH.

J Antibiot (Tokyo). 2012 Jan;65(1):3-8. doi: 10.1038/ja.2011.95. Epub 2011 Nov 9.

20.

Structures and cytotoxic properties of trichoverroids and their macrolide analogues produced by saltwater culture of Myrothecium verrucaria.

Amagata T, Rath C, Rigot JF, Tarlov N, Tenney K, Valeriote FA, Crews P.

J Med Chem. 2003 Sep 25;46(20):4342-50.

PMID:
13678412

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