ライフサイエンスコーパス: diisocyanate

1 linkage, which provide identification of the diisocyanate.

2 subsequently cross-linked with hexamethylene diisocyanate.

3 thesis reaction with 4,4'-methylene diphenyl diisocyanate (4,4'-MDI) circumvents harsh reaction condi

4 onamide (PTSA), (iii) 4,4'-methylenediphenyl diisocyanate (4,4'-MDI), (iv) toluenediisocyanate (TDI),

5 Treatment of the diisocyanate 43 with 2 equiv of the iminophosphorane 7 f

6 nd skin proteins that become conjugated with diisocyanate after in vitro and in vivo exposure.

7 cromolecular alcohols with excess isophorone diisocyanate and subsequent derivatization of the isocya

8 Diisocyanates are asthma-causing chemicals used in the c

9 Diisocyanates are considered as skin and respiratory sen

10 Diisocyanates are highly reactive chemical compounds wid

11 Diisocyanates are the leading cause of occupational asth

12 ntly associated with a clinical diagnosis of diisocyanate asthma (DA).

13 n (56-kD) differed from the predominant lung diisocyanate-conjugated keratin (47-kD).

14 to liquid-phase HDI, although the major skin diisocyanate-conjugated protein (56-kD) differed from th

15 samples, whereas albumin was the predominant diisocyanate-conjugated protein in bronchoalveolar lavag

16 in 18 was also identified as the predominant diisocyanate-conjugated protein in human endobronchial b

17 Keratin was also identified as a predominant diisocyanate-conjugated protein in human skin biopsy sam

18 nase, and actin were identified as prominent diisocyanate-conjugated proteins through use of a combin

19 Introducing an oil-soluble polymeric diisocyanate cross-linker into the oil phase prior to ho

20 Moreover, diisocyanate cross-linking at the oil/water interface le

21 o be an important step in the development of diisocyanate (dNCO)-specific allergic sensitization; how

22 Urinary diamines are biomarkers of diisocyanate exposure.

23 h cross-linking of iohexol and hexamethylene diisocyanate followed by coprecipitation of the resultin

24 Although diisocyanates have been identified as causative agents o

25 ins can become conjugated with hexamethylene diisocyanate (HDI) and may be biologically important in

26 hyde (MDA), glutaraldehyde and hexamethylene diisocyanate (HMDC).

27 We previously reported that diisocyanate-human serum albumin (DIISO-HSA) stimulated

28 nking, diisocyanate self-polymerization, and diisocyanate hydrolysis.

29 on of poly(ethylene glycol) to hexamethylene diisocyanate in solution has been performed.

30 d other proteins as potential "carriers" for diisocyanates in vivo, and suggest that HDI conjugation

31 teins may play a role in the pathogenesis of diisocyanate-induced asthma.

32 e (HDI) and may be biologically important in diisocyanate-induced asthma.

33 Oligomer ions containing the diisocyanate linkage are also observed in the spectrum,

34 observation of oligomer ions containing the diisocyanate linkage, which provide identification of th

35 ustrial intermediate 4,4'-methylene diphenyl diisocyanate (MDI) is thought to be an important step in

36 ustrial MDA mixtures, and methylene diphenyl diisocyanate (MDI) mixtures used in polyurethane synthes

37 ltimeric MDA species, and methylene diphenyl diisocyanate (MDI) mixtures.

38 MDA is a precursor to methylene diphenyl diisocyanate (MDI), a hard block component in polyuretha

39 Diphenylmethane diisocyanate (MDI), the chemical commonly used as a cros

40 ally important isomers, 2,4- and 2,6-toluene diisocyanate, on human serum albumin at varying diisocya

41 Diisocyanate-protein conjugation results in a variety of

42 At a low (1:2) diisocyanate/protein ratio, five binding sites are ident

43 socyanate, on human serum albumin at varying diisocyanate/protein ratios.

44 nderstand the chemical species produced when diisocyanates react with protein, tandem mass spectromet

45 ding intra- and intermolecular crosslinking, diisocyanate self-polymerization, and diisocyanate hydro

46 Exposure to toluene diisocyanate (TDI), an industrially important crosslinki

47 Inhalation of irritants, such as toluene diisocyanate (TDI), stimulates substance P (SP) release

48 p and characterize a murine model of toluene diisocyanate (TDI)-induced rhinitis.

49 GP) molecules are reacted with hexamethylene diisocyanate trimer (HDI) and polyethylene glycol (PEG)

50 ctrum, providing a means for identifying the diisocyanate used for PUR syntheses.

51 ized from poly(vinyl alcohol) and isophorone diisocyanate was performed by covalent attachment to fre

52 ment of exposure to the most common aromatic diisocyanates within targeted groups as well as larger p