ライフサイエンスコーパス: straight chain

1 linear alpha-helices but less extended than straight chains.

2 lenic acids and are characterized by C17-C23 straight chains, 1-3 cis double bonds separated by methy

3 Exposure to straight-chain acids leads to a binary ligand shell that

4 pha)-inducible pathway capable of catalyzing straight-chain acyl-CoAs and a second noninducible pathw

5 ACX1A exhibited a preference for C12 and C14 straight-chain acyl-CoAs and also was active in the meta

6 ator-inducible pathway capable of catalyzing straight-chain acyl-CoAs by fatty acyl-CoA oxidase, L-bi

7 ding a broader range of acyl-HSLs, including straight-chain acyl-HSLs to which LuxR does not respond.

8 ant of LuxR-G2E that retains the response to straight-chain acyl-HSLs, but no longer responds to 3OC6

9 affinity with little difference between the straight-chain alcohol esters (from methyl to n-butyl).

10 ting ligands is increased through the use of straight chain alcohols, ROH, solvation of Pb(2+) is obs

11 e found to increase with the addition of the straight-chain alcohols ethanol, octanol, and to some ex

12 s of the series were those that could form a straight chain aldehyde intermediate after esterase-medi

13 Straight chain aldehydes and alcohols demonstrated signi

14 rs from a homologous series of iso-intensive straight-chain aldehydes that differed serially by only

15 re of fatty acids, an ester, and a series of straight-chain aldehydes.

16 raged peak areas for terpenes, pyrazines and straight-chained aldehydes.

17 ogressively by replacing W26 with non-coded, straight-chain aliphatic amino acids of increasing chain

18 Carbon chain length in several classes of straight-chain aliphatic odorants has been proposed as a

19 Patterns evoked by straight-chained aliphatic odorants confirmed an associa

20 rs have been functionalized with hydrophobic straight chain alkane units (C6, C12, and C18) while the

21 The mass spectrum for a straight-chain alkane mixture (C(21)-C(40)) shows compar

22 Functionalization molecules included straight chain alkanes, anionically charged dye molecule

23 indrical capsule provides an environment for straight-chain alkanes that can properly fill the space

24 rential responses we observed previously for straight-chained alkanes of differing carbon number, the

25 lfactory responses to a homologous series of straight-chained alkanes that consisted of purely hydroc

26 A series of straight chain alkyl amides demonstrated that the optima

27 Two labile straight chain alkyl motifs were developed: a cysteine d

28 esterified with a variety of isoprenoid and straight-chain alkyl alcohols as in FAPs.

29 Straight-chain alkyl amides are one of the few classes o

30 isoflavone with a free 4'-OH function and a straight-chain alkyl substituent at the 7 position that

31 e study the interfacial behavior between the straight-chain alkyl surfactant sodium dodecyl sulfate (

32 Beginning with straight-chain alkyl, amine-terminated self-assembled mo

33 The thermochemistry of straight-chain alkynes and polyynes is very self-consist

34 ction that allowed stepwise incorporation of straight chain amino acid linkers and a bis-benzimidazol

35 ranched hydrophobic substrate but permit the straight-chain amino acids to be used as substrates.The

36 nstitution of acyltransferase activity using straight-chain analogues were unsuccessful, suggesting t

37 ct with residual -OH, whereas, on the longer straight chain anchor, reaction occurs exclusively at th

38 as comprised of a 20:80 (mol/mol) mixture of straight chain and iso-branched isomers, while the corre

39 ovides C.t. with the capacity to incorporate straight-chain and bacterial specific branched-chain fat

40 [M - H](+) is the dominant species for straight-chain and branched alkanes.

41 site discriminates the tertiary structure of straight-chain and branched-chain alcohols and appears t

42 representing 3 amine classes (alkanolamines, straight-chain and cyclic diamines, and amino acids), th

43 cture, the glucose sugar is observed in both straight-chain and ring forms.

44 u protein, arachidonic acid, and a series of straight chain anionic, cationic, and nonionic detergent

45 onization generates abundant ion signals for straight-chain, branched, and cycloalkanes with minimal

46 These straight-chained, branched, cyclic, and double-bonded mo

47 Hydrocarbon structural categories included straight-chained, branched, double-bonded, alicyclic, an

48 aromatic (benzene, toluene, and xylene) and straight-chain (C(5) to C(12)) hydrocarbons present in p

49 pping effects resulting from branched versus straight-chain capping ligands were compared and a possi

50 interstellar medium (ISM) are organic with a straight-chain carbon backbone.

51 ve higher octane numbers compared with their straight-chain counterparts.

52 The emission of straight-chain esters decreased under extremely low O(2)

53 molar K(d) values) in the order: cholesterol straight chain fatty acid > kinked chain fatty acid.

54 Straight chain fatty acid alpha-oxidation increases duri

55 nd suggested to catalyze the initial step of straight chain fatty acid alpha-oxidation.

56 xybutyric acid ((S)-3,4-DHBA), an endogenous straight chain fatty acid, is a normal human urinary met

57 alcohol acetates (HAAs) and ethyl esters of straight chain fatty acids (EEFAs) at the end of ferment

58 paralogue leading to a greater proportion of straight chain fatty acids in the membrane, and the upre

59 pathway involving, in the case of saturated straight chain fatty acids of even carbon number, at lea

60 in, the first two enzymes of the peroxisomal straight-chain fatty acid beta-oxidation pathway, exhibi

61 Initiation of straight-chain fatty acid biosynthesis by the type II FA

62 suggests that a FabH-independent pathway for straight-chain fatty acid biosynthesis operates in S. gl

63 le butyryl-CoA was converted to palmitate (a straight-chain fatty acid).

64 ated 75 (Cys122Ala) to 500% (Cys122Gln) more straight-chain fatty acids (SCFA) than the corresponding

65 uch as Escherichia coli, which generate only straight-chain fatty acids (SCFAs), FabH has a substrate

66 rial oxidation, and esterification of normal straight-chain fatty acids has been studied extensively,

67 efold increase in the cellular levels of the straight-chain fatty acids palmitate and myristate.

68 The production of straight-chain fatty acids produced was significantly co

69 LS) showed that acetates and ethyl esters of straight-chain fatty acids were associated with floral a

70 higher concentrations of the ethyl esters of straight-chain fatty acids, ethyl, hexyl, isoamyl acetat

71 OPDA and OPC-8:0, as well as medium-to-long straight-chain fatty acids.

72 Most of the known signals are straight-chain fatty acyl-HSLs, and evidence indicates t

73 reaction rate, the esterifications of C4-C18 straight-chain fatty alcohol with dihydrocaffeic acid (D

74 r 9c but only 33 for 9d, suggesting that the straight-chained fatty alcohol esters were more therapeu

75 thermophiles may use sugars in both ring and straight chain forms.

76 eased hydrogenolysis rates relative to their straight-chain homologues in both homogeneous and hetero

77 These odorants had a common straight-chain hydrocarbon structure, but differed syste

78 ex food and environmental samples, including straight-chain hydrocarbons, primary alcohols, secondary

79 of alkanes (from six to 16 carbons) that are straight-chained hydrocarbons without functional groups.

80 Unlike conventional PNCs capped with straight-chain ligands, APTES-capped PNCs show high stab

81 tylene spacer group, (2) either a two-carbon straight chain linker or a conformationally restricting

82 are examples synthesized with the two-carbon straight chain linker, whereas 26-31 are analogues prepa

83 SAM formation was also probed for straight-chain molecules, hexadecanethiol and hexadecane

84 -2 H-1-benzopyran linked to a 3-alkylindole (straight chain), more specifically substituted with a 5-

85 A series of straight-chain N5-aminoalkylacyl derivatives demonstrate

86 structural analysis suggests the presence of straight chains of Te atoms ( approximately 3.0 A apart)

87 Straight chain peptide-bound aliphatic phosphates of the

88 orooctanoic acid, has been investigated on a straight-chain perfluorohexyl adsorbent.

89 ention mechanisms of perfluoroalkyl acids on straight-chain perfluorohexyl sorbents are discussed.

90 thyl-bridged organic/inorganic (BEH-C18) and straight-chain perfluorohexylpropyl silica (C6F13), have

91 ugh its B cell ligand has been identified as straight chain poly-N-acetyl-lactosamine (SC-PNAL), the

92 tive pathogen with phospholipids composed of straight chain saturated and monounsaturated fatty acids

93 led to the formation of wax monoesters from straight chain saturated, unsaturated, and polyunsaturat

94 h, rats were exposed to homologous series of straight-chained, saturated aliphatic aldehydes, ethyl e

95 CN), with an abundance 0.4 times that of its straight-chain structural isomer.

96 The transition from ring form to straight-chain substrate is achieved through rotation of

97 sts that pyrococcal PGI has a preference for straight chain substrates and that metabolism in extreme

98 nylzinc reagents derived from both bulky and straight chain terminal alkynes.

99 er the other to form infinite ...Ti-O...Ti-O straight chains with alternating short and long Ti-O dis