ライフサイエンスコーパス: ergot alkaloid

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1 nes) to 10(4.0) L/kg(oc) (positively charged ergot alkaloids).

2 Dihydroergosine was identified as the major ergot alkaloid.

3 The ergot alkaloids, a class of fungal-derived natural produ

4 d to be safe for feed consumption, since the ergot alkaloids and the regulated mycotoxins were below

5 The biosynthesis of the N. fumigata ergot alkaloids and their relation to those produced by

6 ped molecularly imprinted polymer toward six ergot alkaloids and their respective epimers is describe

7 The ergot alkaloids are a diverse class of fungal-derived in

8 d the matrix effect of each of the 12 tested ergot alkaloids as well as a cross-reactivity study with

9 ndole nucleus in the first committed step of ergot alkaloid biosynthesis.

10 that controls this critical branch point of ergot alkaloid biosynthesis.

11 n C. purpurea by its clustering with another ergot alkaloid biosynthetic gene, dmaW.

12 s developed for low-picogram detection of an ergot alkaloid, cabergoline, in coyote plasma extracts.

13 identified for the first time as significant ergot alkaloid components within the C. africana sclerot

14 synthetic pathway of cycloclavine, a complex ergot alkaloid containing a cyclopropyl moiety.

15 The data indicate that ergot alkaloids contribute to virulence of N. fumigata i

16 Ergot alkaloids festuclavine 2 and agroclavine 3 derive

17 alkaloids are associated with the symbionts: ergot alkaloids, indolediterpenes (lolitrems), peramine,

18 e strains of N. fumigata and three different ergot alkaloid mutants derived by previous gene knockout

19 Cycloclavine is a clavine-type Ergot alkaloid noteworthy for its unique pentacyclic ske

20 olites including products of a branch of the ergot alkaloid pathway called fumigaclavines.

21 identify the ergot species by molecular and ergot alkaloid profile analysis, to determine the ergot

22 alkaloid profile analysis, to determine the ergot alkaloid profile in pure honeydew and in infected

23 by previous gene knockouts and differing in ergot alkaloid profiles.

24 Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b)

25 Ergot alkaloids, secondary metabolites produced by filam

26 Elimination of all ergot alkaloids significantly reduced virulence of N. fu

27 amine and aldehyde to form the D ring of the ergot alkaloid structural framework.

28 olites have been described as toxins such as ergot alkaloids that have potent psychotropic activity.

29 We investigated the contribution of ergot alkaloids to virulence of N. fumigata by measuring

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