戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 conversion of the isoflavone formononetin to medicarpin.
2 f the antimicrobial isoflavonoid phytoalexin medicarpin.
3 iently than with cis-(3R,4R)-DMI to give (-)-medicarpin.
4                                              Medicarpin, (3S)-vestitol and (3S)-neovestitol were the
5  for use in studies to selectively eliminate medicarpin accumulation to assess the relative importanc
6 , prior to the increase in IOMT activity and medicarpin accumulation.
7  response through 48 h for compounds such as medicarpin and daidzin; and a lesser delayed and protrac
8 c analysis also revealed the accumulation of medicarpin and its intermediate metabolites.
9                                              Medicarpin and maackiain are antifungal pterocarpan phyt
10 to specifically hydroxylate the phytoalexins medicarpin and maackiain, converting them to less fungit
11 nthesis (chalcone synthase), a key enzyme in medicarpin biosynthesis (isoflavone reductase) and a key
12 sm, and indicate differential mechanisms for medicarpin biosynthesis depending on the nature of elici
13 induced along with other enzymes involved in medicarpin biosynthesis, methylates the A-ring 7-hydroxy
14 ciated with endoplasmic reticulum membranes; medicarpin biosynthetic enzymes have been localized to t
15  alfalfa root isoflavonoids formononetin and medicarpin but not by two triterpenoids present in alfal
16  resulted in accumulation of the phytoalexin medicarpin, coordinated increases in isoflavonoid precur
17 emical mechanisms underlying accumulation of medicarpin differ depending on the nature of the stimulu
18 ction in the biosynthesis of the phytoalexin medicarpin in legumes.
19 es involved in the production of phytoalexin medicarpin in M. truncatula upon infection with P. pachy
20 ula accumulated the isoflavonoid phytoalexin medicarpin in response to yeast elicitor or methyl jasmo
21 ulation to assess the relative importance of medicarpin in the antifungal defense mechanisms of alfal
22 n of formononetin (4'-O-methyl daidzein) and medicarpin in the leaves than does elicitation or infect
23 ylated isoflavonoids such as the phytoalexin medicarpin in vivo, whereas biochemical studies indicate
24                                              Medicarpin inhibited motility of P. penetrans in vitro.
25                   In vitro assay showed that medicarpin inhibited urediniospore germination and diffe
26        The methyl group at the 9 position of medicarpin is generally accepted to arise via the methyl
27 ors to the chiral pterocarpans, (-)- and (+)-medicarpin, respectively.
28                       The total syntheses of medicarpin, sophoracarpan A, and kushecarpin A from a co
29                                              Medicarpin, the major phytoalexin in alfalfa, is synthes
30 NA construct readily metabolized infiltrated medicarpin to 1a-hydroxymedicarpin, indicating high leve
31     Enhanced accumulation of the phytoalexin medicarpin was observed in P. medicaginis-infected leave
32       Constitutive levels of the phytoalexin medicarpin were highest in roots of the two most resista