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 bolized herbicides belonging to the class of phenylurea.
2 bolism, as demonstrated with exogenously fed phenylurea.
3  targeting 52 carbamtes, thiocarbamates, and phenylureas.
4 rolidin-2-yl]methyl}amino)hexyl]-N-methyl-N'-phenylurea (1396-12), but not a structurally related con
5 of phenyl hydroxycarbamate 1 and 1-hydroxy-3-phenylurea 2 using CuCl2 and 2-ethyl-2-oxazoline in meth
6                                              Phenylurea 4a displayed a very efficient binding toward
7 eido dihomooxacalix[4]arene anion receptors (phenylurea 4a, phenylthiourea 4b, and tert-butylurea 4c)
8 dition of the appropriate 1-(acetylphenyl)-3-phenylurea 9a,b to the corresponding isatin 10a-f in eth
9                                       Active phenylurea-based compounds dissociated effector protease
10 plied to tumor cell lines in culture, active phenylurea-based compounds induced apoptosis in a rapid,
11                  Apoptosis induced by active phenylurea-based compounds was blocked by chemical inhib
12 nt with these findings, apoptosis induced by phenylurea-based compounds was not altered by genetic al
13     Altogether, these findings indicate that phenylurea-based XIAP antagonists block interaction of d
14                                              Phenylurea-based XIAP antagonists induced apoptosis (def
15 een of a compound library, we identified the phenylurea BX430 (1-(2,6-dibromo-4-isopropyl-phenyl)-3-(
16 nt, the discovery of a 2-(phenoxypyridine)-3-phenylurea chemotype that inhibited ADP-mediated platele
17  forchlorfenuron N-(2-chloro-4-pyridinyl)-N'-phenylurea (CPPU) is widely used, its effect on grape qu
18           In comparison to related bidentate phenylurea dihomooxacalix[4]arenes, tetraphenylurea 4a i
19 nzothiazole sulfonic acid and 1-cyclohexyl-3-phenylurea from tire wear and denatonium used as a bitte
20 insight into the role of Asn-285 for Gb4 and phenylurea-galabiose binding, suggesting additional hydr
21  interaction with the glycomimetic inhibitor phenylurea-galabiose.
22                          Cholate esters with phenylurea groups at the 7alpha- and 12alpha-positions a
23 s responsible for in situ degradation of the phenylurea herbicide linuron in a BPS matrix.
24                       Isoproturon (IPU) is a phenylurea herbicide used to control broad-leaf grasses
25                     The worldwide use of the phenylurea herbicide, isoproturon (IPU), has resulted in
26 yzes rapid oxidative dealkylation of various phenylurea herbicides to yield nonphytotoxic metabolites
27 10) specifically catalyzed the metabolism of phenylurea herbicides, converting four herbicides of thi
28 trazine and terbutryn, but not by nitrile or phenylurea herbicides.
29  the host-guest binding of a bis(arylethynyl phenylurea) host with a chloride guest in eight solvents
30 tuents at the meta- or para-positions of the phenylurea, increases ligand affinity and beta1-selectiv
31 le following modification of the substituted phenylurea moiety appended off the lysine revealed that
32                                            A phenylurea series of chemical inhibitors of XIAP was rec
33  to three structurally similar groups (i.e., phenylureas, tertiary amides, and tertiary amines).
34   For example, neutral and basic pesticides (phenylureas, triazines) are more sensitive using APCI (e
35                        Phenyl carbamates and phenylureas were synthesized and investigated.
36 lphenoxy)pyridin-3-yl)-3-4-(trifluoromethoxy)phenylurea, which demonstrated a 68 +/- 7% thrombus weig