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1 nd 6-propionyl-2-(dimethylamino)naphthalene (Prodan).
2 esponse to the excited states of Laurdan and Prodan.
3 rent polarity-sensitive probes, Nile red and Prodan.
4 new fluorophores are structurally related to Prodan.
5 e significantly red-shifted when compared to Prodan.
6 ity-sensitive emission comparable to that of PRODAN and displays high quantum yields in a range of so
7                                        Using Prodan and Laurdan as fluorescent membrane probes, phosp
8 es N,N-dimethyl-6-propionyl-2-naphthylamine (prodan) and coumarin 153 (C153) in a series of toluene/d
9 bumins, a hydrophobic fluorescent indicator (PRODAN), and a hydrophobic additive (deoxycholate) to de
10 N), 6-propionyl-2-dimethylamino-naphthalene (PRODAN), and Lissamine rhodamine B 1,2-dihexadecanoyl-sn
11 uorescent probes used (bis-pyrene, nystatin, prodan, and merocyanine) were chosen because they differ
12 ently substituted planar chiral analogues of PRODAN based on a [2.2]paracyclophane scaffold.
13                                          The prodan data supported these results by displaying modest
14                                          The PRODAN derivative bearing a pivaloyl group (4) was prepa
15 olvatochromism that is similar to five other PRODAN derivatives (1-3, 5, 6).
16                             The shape of the prodan emission spectrum detected both liquid-solid and
17 he 6-propionyl-2-(dimethylamino)naphthalene (Prodan) fluorescence spectra for both lipids are consist
18 lene 2-propionyl-6-dimethylaminonaphthalene (PRODAN) fluorophores.
19                        The fluorescent probe Prodan has been widely used as a probe of model and biol
20                   These results suggest that Prodan has preferential interactions with cholesterol, a
21 ent properties and partition coefficients of Prodan in model membranes of phosphatidylcholines and ph
22 f 7HSAP1 with the solvatochromic fluorophore PRODAN indicated that the nanotubes could encapsulate sh
23                 The partition coefficient of Prodan into these lipids also varies with the phase stat
24                  Various fluorescent probes (Prodan, Laurdan, pyrene-labeled fatty acid, and dansyl-l
25         The fluorescence emission spectra of Prodan, Patman, and Laurdan all showed spectral changes
26                   These results suggest that Prodan should be used only with great caution in complex
27                         It is shown that the Prodan spectrum in the presence of cholesterol no longer
28  hydration dynamics, we probed acrylodan and prodan; the latter is bound to domain II.
29 ed the membrane surface exposing some of the Prodan to bulk water.
30 s of 2-propionyl-6-dimethylaminonaphthalene (PRODAN) with twisted carbonyl groups were investigated a