ライフサイエンスコーパス: ergot

1 aily headache patients overuse analgesics or ergots.

2 ced sensitization, whereas the high affinity ergot agonists bromocriptine and lisuride did not.

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

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

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

6 e scaffold, as are present in members of the ergot alkaloid class of natural products.

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

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

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

10 plemented by the synthesis of the polycyclic ergot alkaloid natural product xylanigripone A.

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

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

13 Reconstituting the ergot alkaloid pathway in a strain strongly amenable for

14 Reaction of the isocyanide with an ergot alkaloid precursor results in carbon-carbon bond f

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

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

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

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

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

20 e fescue toxicosis (FT) is caused by grazing ergot alkaloid-producing endophyte (Epichloe coenophiala

21 Dihydroergosine was identified as the major ergot alkaloid.

22 Ergot alkaloids (EA) are mycotoxins produced by Clavicep

23 Ergot alkaloids (EAs) are a group of mycotoxins that con

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

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

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

27 The ergot alkaloids are a class of natural products known fo

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

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

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

31 Ergot alkaloids festuclavine 2 and agroclavine 3 derive

32 The mean recovery rate of ergot alkaloids in spiked whole rye grain was close to 1

33 rized all-in-one 2LabsToGo system to analyze ergot alkaloids in whole rye samples.

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

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

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

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

38 Detectability of ergot alkaloids was proven to be below the current maxim

39 Results of screening whole rye for ergot alkaloids were successfully verified by comparison

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

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

42 ales) that produce the bioactive metabolites ergot alkaloids, indole diterpene alkaloids, and swainso

43 Here, we report the occurrence of ergot alkaloids, indole diterpene alkaloids, and swainso

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

45 nations of oxytocin, carbetocin, carboprost, ergot alkaloids, misoprostol, and tranexamic acid were i

46 Ergot alkaloids, naturally occurring mycotoxins of Clavi

47 al pharmacological agents, such as oxytocin, ergot alkaloids, prostaglandins, and tranexamic acid, ha

48 Ergot alkaloids, secondary metabolites produced by filam

49 , dragmacidins, isoryanodane diterpenes, and ergot alkaloids.

50 ne-I aldehyde 1 represents a branch point in ergot biosynthesis.

51 he Old Yellow Enzyme homologue EasA from the ergot biosynthetic gene cluster of Aspergillus fumigatus

52 ed with dihydroergotamine mesylate (DHE), an ergot derivative that is especially effective in non-res

53 ing lysergic acid dimethylamide (DAM-57), an ergot derivative, and its deuterated isotopologues; we a

54 vasoconstrictor properties (ie, triptans or ergot derivatives).

55 Ropinirole, which is a non-ergot dopamine agonist derivative, exerts therapeutic be

56 elegiline (Spearman's rho 0.22, p=0.005) and ergot dopamine agonists (0.24, p=0.006) but not correlat

57 to 5-hydroxytryptamine (5-HT)(2)-preferring ergot drugs (ergotamine, methysergide).

58 vular 5-HT(2B) receptors by norfenfluramine, ergot drugs, or 5-HT released from carcinoid tumors (wit

59 antioselective; biological methods utilizing ergot fungi, produce an assortment of products that comp

60 human pathogen Sporothrix schenckii, and the ergot fungus Claviceps purpurea.

61 Enzyme encoded in the Aspergillus fumigatus ergot gene cluster catalyzes reduction of the alpha,beta

62 ynthesizing a few alkaloid molecules such as ergot, hapalindole alkaloids, and related heterocyclic c

63 Sorghum ergot is a disease caused commonly by C. africana.

64 e treatment is either specific (triptans and ergots) or non-specific (analgesics).

65 Psilocybe, Amanita, and others, and also the ergot-producing Claviceps and insect-pathogenic Massospo

66 The aims of the study were to identify the ergot species by molecular and ergot alkaloid profile an

67 ble efficacy and tolerability issues, use of ergots to abort attacks has nearly vanished in most coun

68 art disease and valvulopathy associated with ergot use.

69 In 2015, ergot was identified for the first time in sorghum field

70 te migraine-specific medication [triptans or ergots] was used to treat a headache of any severity or