ライフサイエンスコーパス: condensation product

1 hylene, N,N-dimethylcinnamide, and a complex condensation product.

2 5'-phosphate (PLP) by forming a Knoevenagel condensation product.

3 d characterization of the intermediate Aldol condensation product.

4 ak strongly suggested formation of a S3P-PEP condensation product.

5 zole ring enables further elaboration of the condensation products.

6 as generally believed, A2E or other retinoid condensation products.

7 venagel conditions to give a number of novel condensation products.

8 3, 4 + 4, 6 + 6, and 8 + 8 macrocyclic imine condensation products.

9 odynamic product was the isomeric self-aldol condensation product 12.

10 ituent of Brassica vegetables, and its major condensation product, 3,3'-diindolylmethane (DIM), again

11 reacted with o-phenylenediamine to form the condensation product, 3-(dihydroxyethyl)furo[3,4-b]quino

12 The major condensation product, (4aS,6aR,12bS)-2H-9,10-bis(tert-bu

13 The minor condensation product, (4aS,6aS,12bS)-2H-9,10-bis(tert-bu

14 e stomach following ingestion and three acid-condensation products; a dimer, a noncyclic trimer, and

15 all-trans-retinal causes accumulation of its condensation products, A2E, and all-trans-retinal dimer

16 All three I3C acid-condensation products also increased the accumulation of

17 lly differentiated nanotube species produces condensation products and unzipping of nanotubes due to

18 In vitro, the size and shape of the condensation products, and the nanostructures subsequent

19 e formation of the zwitterionic paramagnetic condensation products are analogous to that observed in

20 for the yields of the 5-isocorrole and self-condensation product by HPLC.

21 The resulting condensation product can be reduced in the presence of N

22 cation of pyrroloquinoline quinone (PQQ) and condensation products formed upon incubation of PQQ with

23 formation of anion and zwitterionic radical condensation products from ninhydrin and nitrogen-contai

24 yl)amines and 1-(2,2-diphenylethyl)amines as condensation products in good yields (50-99%).

25 A2E demonstrated the acquisition of retinal condensation products in Mertk(-/-) mouse RPE prior to r

26 s-retinal can lead to the formation of toxic condensation products in the eye.

27 mitted the identification of retinosomes and condensation products in the retinal pigment epithelium

28 These aberrant fluorescent condensation products, including di-retinoid-pyridinium-

29 s expected, that the percentage yield of the condensation products increases and the yield of the hyd

30 The I3C acid-condensation product mixture competed with azidopine for

31 The I3C acid-condensation product mixture, but not I3C, sensitized B1

32 ne and identified two novel, closely related condensation products, named trace-extended aromatic con

33 diretinoid-pyridinium-ethanolamine (A2E), a condensation product of all-trans-retinal and a surrogat

34 resulted in slight overproduction of A2E, a condensation product of all-trans-retinal and phosphatid

35 the mechanism of nanoring self-assembly, the condensation product of CBT-Cys(SEt) formed using differ

36 lots appeared to be tetrahydropentoxyline, a condensation product of glucose and tryptophan.

37 ethane (DIM), a major in vivo acid-catalyzed condensation product of I3C, also showed some benefit in

38 ture and composition of a retan agent, CNSF (condensation product of naphthalenesulfonic acid (NSA) a

39 lipofuscin fluorophore that originates as a condensation product of two molecules of all-trans-retin

40 Fluorescent condensation products of all-trans-retinal accumulate in

41 In order to study condensation products of mononucleotides and hydrolysis

42 But harmful fluorescent condensation products of retinoids also occur in the ret

43 ge-related macular degeneration that deposit condensation products of retinoids.

44 tion products, named trace-extended aromatic condensation products (TEACOPs), which are active at low

45 likely were recruited to transport A2E-like condensation products to the RPE and dispose of the dyin

46 he observed MDR-reversing effect of the acid-condensation products was due to direct interaction with

47 These condensation products were all obtained from simple [2 +

48 PQQ was incubated with amino acids and condensation products were separated by HPLC.

49 he spontaneous formation of an anion radical condensation product, wherein the no. 2 carbon (original

50 ntly influence the favorability of forming a condensation product with a given organic donor.

51 ly arise from free sugar or from Schiff base condensation products with protein amino groups, rather

52 ndantrione anion radical spontaneously forms condensation products with the HMPA to produce a variety