ライフサイエンスコーパス: phenylurea

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1 bolism, as demonstrated with exogenously fed phenylurea.

2 bolized herbicides belonging to the class of 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 Active phenylurea-based compounds dissociated effector protease

9 plied to tumor cell lines in culture, active phenylurea-based compounds induced apoptosis in a rapid,

10 Apoptosis induced by active phenylurea-based compounds was blocked by chemical inhib

11 nt with these findings, apoptosis induced by phenylurea-based compounds was not altered by genetic al

12 Altogether, these findings indicate that phenylurea-based XIAP antagonists block interaction of d

13 Phenylurea-based XIAP antagonists induced apoptosis (def

14 een of a compound library, we identified the phenylurea BX430 (1-(2,6-dibromo-4-isopropyl-phenyl)-3-(

15 nt, the discovery of a 2-(phenoxypyridine)-3-phenylurea chemotype that inhibited ADP-mediated platele

16 In comparison to related bidentate phenylurea dihomooxacalix[4]arenes, tetraphenylurea 4a i

17 Cholate esters with phenylurea groups at the 7alpha- and 12alpha-positions a

18 Isoproturon (IPU) is a phenylurea herbicide used to control broad-leaf grasses

19 The worldwide use of the phenylurea herbicide, isoproturon (IPU), has resulted in

20 yzes rapid oxidative dealkylation of various phenylurea herbicides to yield nonphytotoxic metabolites

21 10) specifically catalyzed the metabolism of phenylurea herbicides, converting four herbicides of thi

22 trazine and terbutryn, but not by nitrile or phenylurea herbicides.

23 tuents at the meta- or para-positions of the phenylurea, increases ligand affinity and beta1-selectiv

24 le following modification of the substituted phenylurea moiety appended off the lysine revealed that

25 A phenylurea series of chemical inhibitors of XIAP was rec

26 to three structurally similar groups (i.e., phenylureas, tertiary amides, and tertiary amines).

27 For example, neutral and basic pesticides (phenylureas, triazines) are more sensitive using APCI (e

28 Phenyl carbamates and phenylureas were synthesized and investigated.

29 lphenoxy)pyridin-3-yl)-3-4-(trifluoromethoxy)phenylurea, which demonstrated a 68 +/- 7% thrombus weig

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