ライフサイエンスコーパス: penta-

1 lly dispersed on the support surface (Pt/Al3+penta = 1), whereas two-dimensional Pt rafts form at hig

2 oncentrations of 14 PBDE congeners including penta (28, 47, 99, 100, 153, 154), octa (183, 196, 197,

3 etected in the CCC fractions (12 tetra-, 117 penta-, 81 hexa-, and 17 heptachlorinated OH-CTTs), whic

4 rocyclic and linear isomers were detected in penta- and heptameric assemblies; in the larger octa- an

5 utants retain the ability to synthesize some penta- and hexa-acylated lipid A molecules because of li

6 d lipopolysaccharide (LPS) with a variety of penta- and hexa-acylated lipid A structures under differ

7 Specifically, caspase-11 responds to penta- and hexa-acylated lipid A, whereas tetra-acylated

8 ogeneous mixture of lipid A structures, with penta- and hexa-acylated structures containing one and t

9 orewater concentrations, by >90% for tetra-, penta- and hexa-clorinated congeners to 60-70% for octac

10 d NO(-), respectively, to yield a mixture of penta- and hexa-coordinate nitrosylated cyt c.

11 In contrast, penta- and hexa-O-galloyl-glucose induced greatest and m

12 These strains accumulated penta- and hexaacylated free lipid A containing a second

13 LpxL and LpxM, resulting in the synthesis of penta- and hexaacylated lipid A, which is optimal for th

14 akthrough of high-volume sampler filters for penta- and hexachlorobenzene and semiquantitative values

15 .042) for most groups, with the exception of penta- and hexachlorobiphenyls, DDE and mirex.

16 eflecting changes in the equilibrium between penta- and hexacoordinate heme species in the enzyme.

17 The concept of planar hypercoordinate (e.g., penta- and hexacoordinate) carbons is intriguing as it i

18 glutamate analogue) and 36% of D1694 (mostly penta- and hexaglutamates) remained in the cells.

19 s for cytotoxicity, was anabolized mostly to penta- and hexaglutamates, whereas approximately 80% of

20 ed in very strong amplification of the large penta- and hexameric macrocycles.

21 mes cleave tri- and tetramers of GlcNAc from penta- and hexameric oligomers and are unable to cleave

22 F in a stepwise sequential manner, but novel penta- and hexapeptides as well as tri- and tetrapeptide

23 However, for larger penta- and hexasaccharides (LNF-1 and LND-1), the anisot

24 of 2013, which may reflect the phase-out of penta- and octa-BDE mixtures has led to significant decl

25 A mass inventory of penta- and octa-BDEs in Toronto was estimated to be 200

26 al trends are consistent with the removal of penta- and octa-PBDEs from the global market.

27 emissions of 0.4-4 tonnes.y(-1) for each of penta- and octaBDE and 0.35-3.5 tonnes.y(-1) for decaBDE

28 The stocks of penta- and octaBDE peaked in in-use products at 17,000 (

29 Acute 48-h nominal LC50 values for penta- and octabromodiphenyl ether (pentaBDE, octaBDE),

30 A structural heterogeneity, containing both penta- and tetra-acylated lipid A structures.

31 Although the penta- and tetra-CNs (predominantly CN-52/60 and CN-42)

32 emistry is described with a system involving penta- and tetracationic intermediates.

33 iated by the signaling nucleotides guanosine penta- and tetraphosphate (ppGpp).

34 PBP2a can cross-link glycan strands bearing penta- and triglycine, but not monoglycine, and experime

35 and diazenes for the oxidative synthesis of penta- and trisubstituted pyrroles: a nitrenoid analogue

36 By contrast, serum concentrations of tetra-, penta-, and hexa-BDEs were lowest in the youngest childr

37 alyzes the hydrolysis of diadenosine tetra-, penta-, and hexa-phosphates with a preference for diaden

38 The planar tetra-, penta-, and hexacoordinate boron are the prevalent struc

39 A large number of planar tetra-, penta-, and hexacoordinate carbon (local-minimum) struct

40 of microsatellite (mono-, di-, tri-, tetra-, penta-, and hexanucleotide repeats) are found in excess,

41 PnhA hydrolyzes diadenosine tetra-, penta-, and hexaphosphates with a preference for diadeno

42 ient conditions for the synthesis of tetra-, penta-, and hexasubstituted derivatives of 1,4-dihydropy

43 MOS-IV, MOS-V and MOS-VI consist of tetra-, penta-, hexa-, and hepta-saccharides with molecular weig

44 Total consumption of penta-, octa-, and decaBDE from 1970 to 2020 in products

45 10-150, and 200-2000 g.capita(-1).y(-1) for penta-, octa-, and decaBDE, respectively, over the time

46 be transported as efficiently by MsbA as are penta- or hexa-acylated lipid A species.

47 sumption that MsbA is optimized to transport penta- or hexaacylated lipid A, we overexpressed the lau

48 ol with boric acid and are likely to contain penta- or hexacoordinated vanadium rather than tetracooo

49 zinc bioavailability is inositol hexa- (and penta-) phosphate or phytate.

50 prehensive study of the planar tetra- (ptC), penta- (ppC), and hexacoordinate carbon (phC) by coverin

51 this element, which promotes binding of the penta- rather than that of the dipeptide.

52 ries an unmodified aromatic chromophore, the penta- through decaketides have undergone oxidative cycl

53 Half-lives of 1.5-3 min were found for penta- to mono-acetylation of H3, dynamically acetylated

54 s enzyme is active as a monomer, prefers the penta- to the monoglutamyl form of 5-CHO-H(4)PteGlu(n),

55 ors having different glycine branch lengths (penta-, tri-, or monoglycine), while PBP2a can only cros

56 of underacylated endotoxins (i.e., tetra- or penta- vs hexa-acylated) is determined by post-CD14 inte