ライフサイエンスコーパス: BODIPY

1 hearts were examined for presence of NPs and BODIPY.

2 ttached to the aryl at the meso positions of BODIPY.

3 t impact on J-aggregates and fluorescence of BODIPYs.

4 s the first example of heterocycle[ a]-fused BODIPYs.

5 provide a general solution for water-soluble BODIPYs.

6 n the UV-vis and fluorescence spectra of the BODIPYs 1-17 were discussed on the basis of DFT and TDDF

7 bstituted di-, tri-, tetra-, and pentachloro-BODIPYs 2-5 were prepared.

8 The crystal structure of azaBODIPY-(BODIPY)2 triad revealed that the two BODIPY units were i

9 linked azaBODIPY-BODIPY dyads and azaBODIPY-(BODIPY)2 triads.

10 The single crystal structures of BODIPYs 2a and 2b reflect the planar orientation of meso

11 ation of an unprecedented 8-heteroaryl-fused BODIPY 4.

12 interactions, meso-(4-pyridinyl)-substituted BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) dyes

13 Fmoc-Trp(C2-BODIPY)-OH contains a BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) fluo

14 The [a]phenanthrene-fused BODIPYs 4a-c were characterized by NMR spectroscopy, HRM

15 In addition, BODIPYs 4b and 4c exhibit no toxicity in the light or da

16 tivation, staining intracellular lipids with BODIPY(505/515), and FACS-based isolation of top 0.5% li

17 With surfactant micelles, oxidation of BODIPY(665/676) was observed.

18 ns containing an oxidizable fluorescent dye, BODIPY(665/676), was blended with a soybean oil-in-water

19 cal microscopy using radical-sensitive probe BODIPY(665/676).

20 BODIPY 7 bearing thienyl groups on the 2 and 6 positions

21 o-glycolic acid) (PLGA) NPs were loaded with BODIPY, a fluorophore, and percutaneously administered i

22 le light where the two dye molecules (Ru and Bodipy) absorb with equal probability leads to the coope

23 lectrophiles, we have designed a fluorogenic BODIPY-acrolein probe, AcroB, that undergoes a >350-fold

24 s of BODIPY-ATP resulted in the formation of BODIPY-adenosine and phosphate ions.

25 The fluorescence of the generated BODIPY-adenosine was insensitive to the change in the co

26 ize the smallest possible noncovalent H-type BODIPY aggregate, namely, an H-dimer.

27 IYIY-I2-BODIPY alone and in combination with PDT modulates the i

28 We have developed a fluorogenic Trp-BODIPY amino acid with a spacer-free C-C linkage between

29 in the literature that describes the use of BODIPY analogs for detecting alkaline phosphatase (ALP)

30 toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs.

31 Fluorescent boron dipyrromethene (BODIPY) analogs are often used as sensors for detecting

32 e photophysical properties of pyridine-based BODIPY analogues, dipyridylmethene dyes.

33 erocyclization of the 3-(dimethylaminovinyl)-BODIPY and 3,5-bis(dimethylaminovinyl)-BODIPY results in

34 arge-separated state composed of an oxidized Bodipy and a reduced Ru.

35 udies indicated a weak interaction among the BODIPY and azaBODIPY moieties and the moieties retain th

36 mphiphilic arrays containing PEG-substituted BODIPY and chlorins or bacteriochlorins were prepared an

37 gid structural conformation of the precursor BODIPY and the high reactivity of its 1,7-bromo groups.

38 are the sum of the individual chromophores (Bodipy and the PtN2S2 moieties), indicating little elect

39 thod for the synthesis of COO-BODIPYs from F-BODIPYs and carboxylic acids is established.

40 l-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene (Bodipy) and a Ru(II)(bipyridine)3 (Ru) derivative-which

41 t, IYIY-diiodo-boron-dipyrromethene (IYIY-I2-BODIPY) and its scrambled counterpart YIYI-I2-BODIPY hav

42 regioselectively from 2,3,5,6,8-pentachloro-BODIPY, and characterized by NMR spectroscopy, HRMS, and

43 ors: beta-scorpion toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs.

44 families of fluorophores (such as coumarin, BODIPY, and oxygen/carbon/silicon-rhodamine), and could

45 complexes, A3-, A2B- and AB2-type corroles, BODIPYs, and their dipyrrane precursors was studied util

46 d antioxidant (chromanol) and prooxidant (Br-BODIPY) antagonistic chemical activities of the two-segm

47 Heavy atom-free BODIPY-anthracene dyads (BADs) generate locally excited

48 Cryptopyrrole-derived oligo-BODIPYs are characterized by a tight intramolecular arra

49 s using 1,3,5,7-tetramethyl-2,6-dicarbethoxy-BODIPY as the universal starting platform.

50 tion light source for the analyte-responsive BODIPY as well as intrinsic reference.

51 t the potential use of [a]phenanthrene-fused BODIPYs as NIR bioimaging probes.

52 For both series of arrays, excitation of BODIPY at 500 nm results in efficient energy transfer to

53 he Fe(III)-induced fluorescence quenching of BODIPY-ATP can be paired with its ALP-mediated dephospho

54 The ALP-catalyzed hydrolysis of BODIPY-ATP resulted in the formation of BODIPY-adenosine

55 of BODIPY-conjugated adenosine triphosphate (BODIPY-ATP) was quenched by Fe(III) ions through photoin

56 of the fluorescence quenching efficiency of BODIPY-AuNPs in the presence of thiols can achieve a lar

57 vatives, with absorption between 500-700 nm, BODIPY-bacteriochlorin arrays should allow for construct

58 ntitatively designed a boron dipyrromethene (BODIPY)-based AIEgen which exhibits (almost) barrierless

59 These boron-dipyrromethene (BODIPY)-based molecular rotors are rigidochromic by mean

60 th narrow-band NIR emission by introducing a BODIPY-based assistant polymer donor as D(1) .

61 Luminescence properties of the BODIPY-based chemodosimetric reagent make it an ideal ca

62 oieties conjugated to nonpolar coumarin- and BODIPY-based fluorophores.

63 , we report synthesis and application of new BODIPY-based hydrophobic sensors (HPsensors) that are st

64 are challenging to implement when developing BODIPY-based indicators: direct modification of BODIPY c

65 We report a BODIPY-based luminescence ON reagent for detection of HN

66 We have designed a BODIPY-based probe called (S)-Sulfox-1, which is equippe

67 We previously reported a BODIPY-based zinc probe, ZincBY-1, that can be used at w

68 further functionalize them to access 13 new, BODIPY-based, voltage-sensitive fluorophores (VF).

69 T-BODIPY) was synthesized by the reaction of BODIPY bearing double terminal ethynyl groups with azido

70 In this study, we show that BODIPYs bearing a sulfonated aromatic group at the meso

71 A series of push-pull BODIPYs bearing multiple electron-donating and electron-

72 c substitution and led to the isolation of F-BODIPYs bearing terminal bromovinyl and enol substituent

73 IYIY-I2-BODIPY binds TrkC similar to neurotrophin-3 (NT-3), and

74 The results of our studies demonstrate that BODIPY bioconjugates bearing the EGFR-targeting peptide

75 A series of five boron dipyrromethene (BODIPY) bioconjugates containing an epidermal growth fac

76 ctron donating group at the meso position of BODIPY blue shifts the absorption and emission with decr

77 me imaging microscopy of the molecular rotor BODIPY C10 in the membranes of live Escherichia coli bac

78 ppressive conventional chemotherapy, IYIY-I2-BODIPY can act as an immune-stimulatory chemotherapeutic

79 reaction is an interesting synthetic tool in BODIPY chemistry, mainly because it allows a valuable re

80 t here the synthesis and characterization of BODIPY-chlorin arrays containing a chlorin subunit, with

81 ce of thiols, meso-(4-pyridinyl)-substituted BODIPY chromophore were displaced and released from the

82 uoroionophore based on a bright red-emitting BODIPY chromophore.

83 rfaces and thus restored the fluorescence of BODIPY chromophore.

84 carbon monoxide-releasing molecules based on BODIPY chromophores (COR-BDPs) activatable by visible-to

85 ylbutadiene-conjugated or styrene-conjugated BODIPY chromophores (PBD-BODIPY or STY-BODIPY, respectiv

86 s were instead observed between at least two BODIPY chromophores along the edges of the cages, arisin

87 ultrafast dynamics of electronically excited BODIPY chromophores could lead to further advances in th

88 e report a set of Fe(II)4L6 cages containing BODIPY chromophores having tuneable photosensitizing pro

89 ompare the ultrafast dynamics of halogenated BODIPY chromophores through applying two-dimensional ele

90 able regioselective postfunctionalization of BODIPY chromophores with different functional groups.

91 ompare the results of structurally different BODIPY chromophores.

92 es, as well as mixed cages that contain both BODIPY chromophores.

93 ctronic states of the structurally different BODIPY chromophores.

94 p element analogues of boron-dipyrromethene (BODIPY) chromophores are described.

95 Boron-dipyrromethene (BODIPY) chromophores have a wide range of applications,

96 ht-activated release of bioactive compounds (BODIPY, colchicine, paclitaxel, and methotrexate) from m

97 s improved access to a fluorogenic tetrazine-BODIPY conjugate.

98 is study discovered that the fluorescence of BODIPY-conjugated adenosine triphosphate (BODIPY-ATP) wa

99 The coumarin- and BODIPY-conjugated amine probes described here undergo 38

100 n P-gp (IC(50) 2.4 +/- 0.6 uM); however, the BODIPY-conjugated derivative of 8 (compound 24) was not

101 us human HT-29 xenografts revealed that only BODIPY conjugates bearing the LARLLT peptide showed tumo

102 Here, we employ conventional BODIPY conjugates for live-cell SMLM via their previousl

103 Our reported SMLM capability of conventional BODIPY conjugates is further demonstrated by imaging lys

104 eacted with BF(3).OEt(2) to afford azaBODIPY-BODIPY conjugates or reacted with metal salt such as Pd(

105 All BODIPY conjugates showed low cytotoxicity (IC(50) > 94 m

106 The BODIPY conjugates with a LARLLT peptide were found to bi

107 DIPY (weak response) at 10 mg/kg, but not I2-BODIPY control, increased the levels of IL-2, IL-4, IL-6

108 IPY-based indicators: direct modification of BODIPY core can disrupt the electronics of the dye, comp

109 hen formulated with a PBD-lipid containing a BODIPY core, indole linker, and PEG length between 1000

110 viscosity-sensitive fluorophores based on a BODIPY core, termed "molecular rotors", in combination w

111 ective formation of the 2-pyridone[ a]-fused BODIPY core, which is the first example of heterocycle[

112 anar orientation of meso substituent and the BODIPY core, which leads to close pi-pi stacking.

113 onic communication between the 8-OPh and the BODIPY core.

114 PET)-capable subunit in meso-position of the BODIPY core.

115 espective of the substitution pattern on the BODIPY core.

116 perties via changes at the 5-position of the BODIPY core.

117 Relying on the boron-dipyrromethene (BODIPY) core, all the probes as well as selected referen

118 aration of the labeled antimicrobial peptide BODIPY-cPAF26 by solid-phase synthesis (6-7 d) and its s

119 an example, we include a procedure for using BODIPY-cPAF26 for wash-free imaging of fungal pathogens,

120 mine), and pharmacological dissection of two BODIPY-cyclopamine binding sites.

121 ed with nanoluciferase (Nluc) and binding of BODIPY-cyclopamine is assessed by quantifying resonance

122 istinction of two separate binding sites for BODIPY-cyclopamine on the SMO transmembrane core in live

123 ready precursors of ortho-substituted 8-aryl BODIPY derivatives by reaction with borontrifluoride eth

124 absorbing and emitting bacteriochlorin, and BODIPY derivatives with different absorption bands in th

125 e encapsulation of three structurally simple BODIPY derivatives within the hydrophobic cavity of a wa

126 Given the availability of diverse BODIPY derivatives, with absorption between 500-700 nm,

127 Boron dipyrromethene (BODIPY) derivatives have found widespread utility as chr

128 thine- and aza-bridged boron dipyrromethene (BODIPY) derivatives were synthesized and systematically

129 We also found that N-BODIPY detects aggregation of peroxisomes during final s

130 A and pore-network development and increased BODIPY diffusion coefficient, resulting in faster releas

131 he different regions of the heart influenced BODIPY distribution, with fluorophore penetrating more r

132 3.Et2O to obtain covalently linked azaBODIPY-BODIPY dyads and azaBODIPY-(BODIPY)2 triads.

133 Moreover, an oil phase doped with an aza-BODIPY dye allows indication of H(2) O(2) in the aqueous

134 tion range can be tuned by the choice of aza-BODIPY dye or/and the hydrogel matrix.

135 applies to a maleimide derivative carrying a BODIPY dye which was chosen for its fluorescence to be o

136 t example of the use of a molecular rotor, a BODIPY dye, to quantitatively visualize the viscosity of

137 irms this fluorescence to originate from the BODIPY dye.

138 ts of a Br-substituted boron-dipyrromethene (BODIPY) dye.

139 oparticle (DLNP) system containing PEGylated BODIPY dyes (PBD) for mRNA delivery and near-infrared (N

140 For instance, the optical properties of BODIPY dyes are inherently related to the degree of aggr

141 e the electronic properties of water-soluble BODIPY dyes for functional indicators.

142 ereas the noncovalent aggregation of various BODIPY dyes has been studied in diverse media, the ill-d

143 ith the outstanding absorption properties of BODIPY dyes lead to photocages with uncaging cross secti

144 tecting groups derived from meso-substituted BODIPY dyes release acetic acid with green wavelengths >

145 Improving the water-solubility of BODIPY dyes remains an outstanding challenge.

146 -PMHC and related bromo and iodo-substituted BODIPY dyes show that the trap segment provides a total

147 The development of water-soluble BODIPY dyes usually involves direct modification of the

148 Eleven formyl-containing BODIPY dyes were prepared by means of either the Liebesk

149 nd lasing properties of the benzofuran-fused BODIPY dyes were thoroughly analyzed with the aid of ele

150 BODIPY dyes with a pendant thioether attached at the mes

151 ersion nanoparticles (UCNP) and pH sensitive BODIPY dyes with tunable p K(a) values embedded into a p

152 lified by the preparation of a series of new BODIPY dyes with unprecedented substitution patterns all

153 lectron deficient backbones, the BF2 unit of BODIPY dyes, and AlF or GaF3 units coordinated to multid

154 asserini reaction to give highly substituted BODIPY dyes.

155 d 6 to give a new family of benzofuran-fused BODIPY dyes.

156 so-enamine-substituted boron dipyrromethene (BODIPY) dyes were found to exhibit favorable indication

157 nstructed from extended borondipyrromethene (BODIPY) dyes, diketopyrrolopyrrole (DPP) dyes, and elect

158 glet oxygen-generating boron-dipyrromethene (BODIPY) dyes.

159 helated tetraarylazadipyrromethene dyes (aza-BODIPYs) dyes physically entrapped in polyurethane hydro

160 Only IYIY-I2-BODIPY enhanced the IFN-gamma(+) and IL-17(+) T-lymphocy

161 ve emission from bacteriochlorin moiety upon BODIPY excitation.

162 The BODIPYs exhibited low dark toxicity and phototoxicity to

163 ysis kinetics and were active in hydrolysing BODIPY-FL casein to varying extents at postmortem aging

164 BODIPY-FL-pentanoic-acid staining revealed higher short

165 reduction to the hydroquinone form, B-VKQH2, BODIPY fluorescence is restored, with emission quantum y

166 n thinner sheet packages which still exhibit BODIPY fluorescence right at the rim of these packages.

167 The incorporation of our unique BODIPY fluorogen in biologically relevant peptides will

168 a spacer-free C-C linkage between Trp and a BODIPY fluorogen, which shows remarkable fluorescence en

169 by confocal fluorescence microscopy using a Bodipy fluorogenic substrate.

170 usually involves direct modification of the BODIPY fluorophore core with ionizable groups or substit

171 binding drug risedronate to a pH-activatable BODIPY fluorophore enables the probe to penetrate osteoc

172 of a new fluorescent probe (BOFP) in which a BODIPY fluorophore has been conjugated to an oxazole-ben

173 bstituents in the context of a water-soluble BODIPY fluorophore provides opportunities to tune the el

174 ese probes incorporate a viscosity-sensitive BODIPY fluorophore that allows the measurement of micros

175 etween the photochrome and a co-encapsulated BODIPY fluorophore.

176 ne redox center), to a boron-dipyrromethene (BODIPY) fluorophore (a lipophilic reporter segment).

177 oquinone, coupled to a boron-dipyrromethene (BODIPY) fluorophore segment that both imparts lipophilic

178 d to the synthesis of heterocycles including BODIPY fluorophores and biotin.

179 es can guide future design of functionalized BODIPYs for various applications, including bioimaging a

180 g cleaves irreversibly to bring the adjacent BODIPY fragment in conjugation with an indole heterocycl

181 aightforward method for the synthesis of COO-BODIPYs from F-BODIPYs and carboxylic acids is establish

182 emical detection of eserine (a pesticide) on BODIPY functionalized SWCNTs as a three dimensional (3D)

183 A series of seven BODIPYs functionalized with ortho-carborane groups at th

184 ar weight (Mw), water uptake, mass loss, and BODIPY (green-fluorescent dye) diffusion coefficient in

185 ODIPY) and its scrambled counterpart YIYI-I2-BODIPY have been prepared.

186 7-tetramethyl-4-bora-3a,4a-diaza-s-indacene (BODIPY) having double terminal ethynyl groups was synthe

187 riplet excited lifetime in a heavy atom-free bodipy helicene molecule.

188 In this work, a N-B-O type BODIPY- hexylcarbazole derivative named BoCz-Lip was rat

189 sional single walled carbon nanotube (SWCNT)-BODIPY hybrid material (3D SWCNT-BODIPY) was synthesized

190 bon electrode (GCE) was modified by 3D SWCNT-BODIPY hybrid material for the determination of eserine

191 BODIPY-hydroporphyrin energy transfer arrays allow for d

192 he immunological impacts mediated by IYIY-I2-BODIPY in pre- and post-PDT conditions.

193 two commonly used fluorescent dyes, DiO and BODIPY, in 10 nm Nanodiscs.

194 monstrated on the basis of selected starting BODIPYs, including polyhalogenated and/or asymmetrical s

195 the boron center often renders the resultant BODIPY incompatible with the chemical transformations re

196 T effects (drug-light interval 1 h), IYIY-I2-BODIPY induced stronger responses.

197 cedures (e.g., asymmetrically functionalized BODIPYs involving halogenated positions) can now be made

198 ositions of chlorin, and a second type where BODIPY is attached at the 10-position of chlorin through

199 ontrast to this, some of the arrays in which BODIPY is attached at the 3- or at both 3,13-positons of

200 The pentachloro-BODIPY is shown to undergo regioselective Pd(0)-catalyze

201 this work, the energy donor moiety (distyryl-BODIPY) is connected to a photosensitizer (i.e., diiodo-

202 4,4-difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) is reported.

203 ized as acceptors: beta-scorpion toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs.

204 Interestingly, a CF(3)-substituted BODIPY, known for forming J-type aggregates, was also en

205 A BODIPY-labeled analogue binds proteins including PDIA1,

206 Three different Bodipy-labeled, Nav1.4-targeting toxins were synthesized

207 nt Arabidopsis mutant atg5 correlated with N-BODIPY labeling.

208 clization of the 1,3-bis(dimethylaminovinyl)-BODIPY leads to the regioselective formation of the 2-py

209 ew approach is generalizable for controlling BODIPY localization and was validated by sensitization o

210 All BODIPYs localized mainly within the cell ER.

211 frared (NIR) thanks to delocalisation of the BODIPY low-lying lowest unoccupied molecular orbital (LU

212 is study clearly indicates that the 3D SWCNT-BODIPY modified electrode tested as an electrochemical s

213 60 nM and 528 nM for eserine on the 3D SWCNT-BODIPY modified electrode, respectively.

214 Two types of arrays were examined: one where BODIPY moieties are attached through a phenylacetylene l

215 ep-red (641-685 nm) emission, and one or two BODIPY moieties, absorbing at 504 nm.

216 containing one or the other of two distinct BODIPY moieties, as well as mixed cages that contain bot

217 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) moieties, which we symmetrically conjugate with

218 to various chain lengths of ethylene-bridged BODIPY motifs was discovered.

219 ies higher than that in the reference dyads (Bodipy-NDI and TAPD-Ru), leading to the energy efficienc

220 tude compared to that in the reference dyads Bodipy-NDI and TAPD-Ru, as it passes from about 3 ns in

221 The tetrad Bodipy-NDI-TAPD-Ru is composed of two different dyes-4,4

222 ural heavier main group element analogues of BODIPY offer a glimpse into the potential for elaboratio

223 is of the fluorogenic amino acid Fmoc-Trp(C2-BODIPY)-OH (3-4 d), the preparation of the labeled antim

224 rp)-based fluorogenic amino acid Fmoc-Trp(C2-BODIPY)-OH and its incorporation into peptides for live-

225 Fmoc-Trp(C2-BODIPY)-OH contains a BODIPY (4,4-difluoro-4-bora-3a,4a-

226 styrene-conjugated BODIPY chromophores (PBD-BODIPY or STY-BODIPY, respectively) as signal carriers t

227 the environmentally insensitive fluorophore BODIPY or the pH-sensitive dye pHrodo red.

228 azines linked to either a peptide, d-biotin, BODIPY, or N-acetyl-d-galactosamine.

229 however, exogenous NBD-phosphatidylcholine, Bodipy-PE, and TopFluor-cholesterol were rapidly traffic

230 ditive, for example, a 2,6-diiodo-B-dimethyl BODIPY photocage features quantum yields of 28% for the

231 y that is 50-fold higher than the best known BODIPY photocages absorbing >600 nm, validating the effe

232 BODIPY photocages allow the release of substrates using

233 Here, we show that boron-alkylated BODIPY photocages are capable of directly photoreleasing

234 Peripherally disulfonated BODIPY photocages are cell impermeable, making them usef

235 ease efficiency of long-wavelength absorbing BODIPY photocages by synthesizing structures that block

236 conventional 2,6-sulfonation to meso-methyl BODIPY photocages is incompatible with their photoreacti

237 conformationally restrained boron-methylated BODIPY photocages that absorb light strongly around 700

238 Toward this goal, we recently reported BODIPY photocages that absorb near-IR light.

239 ent a simple, remote sulfonation solution to BODIPY photocages that imparts water solubility and prov

240 Halogenated BODIPY photoredox catalysts were additionally employed t

241 and photochemical reactivity of meso-methyl BODIPY photoremovable protecting groups was accomplished

242 uct, EA-BPS, that contains both a brominated BODIPY photosensitizer (BPS) and an ethacrynic acid (EA)

243 attempt to develop photostable and efficient BODIPY (PM) dyes for use in liquid dye lasers, three new

244 romomycin A3 assay), and lipid peroxidation (Bodipy probe) in 18 infertile men with grade II or III v

245 d AzG-1, a cyclooctyne- and azide-containing BODIPY probe, respectively, which specifically label int

246 4'-di fl uoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) probes is systematically investigated to demonst

247 BODIPY proved to have a long-term presence within the he

248 th a variety of azido derivatives, including Bodipy, pyrene and ferrocene, was carried out first.

249 on withdrawing group at the meso position of BODIPY red shifts the absorption and emission with enhan

250 f the final charge-separated state (oxidized Bodipy/reduced Ru) in the tetrad lies higher than that i

251 gated BODIPY chromophores (PBD-BODIPY or STY-BODIPY, respectively) as signal carriers that co-autoxid

252 ono-2-pyridone- and bis-2-pyridone[ b]-fused BODIPYs, respectively, similar heterocyclization of the

253 ectroscopy, we confirmed that the ISC of the bodipy results from its twisted molecular structure and

254 inyl)-BODIPY and 3,5-bis(dimethylaminovinyl)-BODIPY results in the formation of mono-2-pyridone- and

255 cell-surface receptors, while monosulfonated BODIPY retains the ability to cross the cellular membran

256 of neutral lipids using a fluorescent probe (BODIPY) revealed that dopaminergic neurons and midbrain

257 Fluorophores based on the BODIPY scaffold are prized for their tunable excitation

258 For both BODIPY scaffolds, halogenation was shown as a general me

259 nanoparticles constructed with such helical bodipy show efficient PDT-mediated antitumor immunity am

260 In vitro, fluorescent CLR1404-BODIPY showed significant selective uptake in a variety

261 The BODIPYs showed higher permeabilities than lucifer yellow

262 The twisted bodipy shows intense long wavelength absorption (e=1.76x

263 In this way, the BODIPY-squaraine conjugates combine the best properties

264 We demonstrated that IYIY-I2-BODIPY (strong response) and YIYI-I2-BODIPY (weak respon

265 which have recently been located for simple BODIPY structures from excited state dynamic simulations

266 In a tandem solar cell comprising a NIR BODIPY subcell and a matching "green" absorber subcell,

267 character exhibited by the bis(aminophenyl)-BODIPY subcomponents disappeared.

268 eric demand of the alkyl substituents in the BODIPY subunit defines the site of (1)O2 addition.

269 Our novel halogenated BODIPY-tetrazine probes only become efficient photosensi

270 structural similarities with well-known aza-BODIPYs, the new MB-DIPYs differ remarkably from them in

271 methane-tetramethylrhodamine-(+/-)CGP 12177 (BODIPY-TMR-CGP)] at the human beta1-adrenoceptor express

272 to a photosensitizer (i.e., diiodo-distyryl-BODIPY) to form a dyad molecule (RET-BDP).

273 Moreover, photoirradiated IYIY-I2-BODIPY treated mice had high levels of effector T-cells

274 optive transfer of immune cells from IYIY-I2-BODIPY-treated survivor mice that were photoirradiated g

275 the fluorescent-dye conjugate, [S14R, W50Pra(Bodipy)]Ts1, we confirmed its binding to Nav1.4 through

276 ional groups was approached with a dual-mode BODIPY-type fluorescence label, which allows quantificat

277 The application of a multimode BODIPY-type fluorescence, photometry, and X-ray photoele

278 supported an efficient energy transfer from BODIPY unit(s) to azaBODIPY unit in dyads and triads.

279 we found that the mutual orientation of two BODIPY units in the cage's cavity was remarkably similar

280 BODIPY-(BODIPY)2 triad revealed that the two BODIPY units were in perpendicular orientation with azaB

281 of aggregation and the mutual orientation of BODIPY units within these aggregates.

282 of 2-pyridone[ a]- and 2-pyridone[ b]-fused BODIPYs using 1,3,5,7-tetramethyl-2,6-dicarbethoxy-BODIP

283 ignificantly inhibited boron-dipyrromethene (BODIPY)-verapamil transport mediated by human P-gp (IC(5

284 The most sensitive of these BODIPY VF dyes displays a 48% DeltaF/F per 100 mV in mam

285 Two additional BODIPY VFs show good voltage sensitivity (>=24% DeltaF/F

286 s were mostly confined to epicardial layers, BODIPY was capable of penetrating into the myocardium, r

287 ective formation of the 2-pyridone[ a]-fused BODIPY was further confirmed by X-ray crystallography an

288 Absorption band of BODIPY was tuned by installation of 0, 1, or 2 styryl su

289 ctroscopic and electrochemical properties of BODIPYs was investigated.

290 chelated tetraarylazadipyrromethene dye (aza-BODIPY) was incorporated into the polyvinylpyrrolidone s

291 ube (SWCNT)-BODIPY hybrid material (3D SWCNT-BODIPY) was synthesized by the reaction of BODIPY bearin

292 ghlight the utility of these new, sulfonated BODIPYs, we further functionalize them to access 13 new,

293 IYIY-I2-BODIPY (strong response) and YIYI-I2-BODIPY (weak response) at 10 mg/kg, but not I2-BODIPY co

294 w fluorescence quantum yields, the push-pull BODIPYS were effective for cell imaging, readily accumul

295 All BODIPYs were nontoxic in the dark (IC50 > 200 muM) and s

296 xisome abundance using the small probe Nitro-BODIPY, which in vivo fluoresces selectively inside pero

297 ine the route to a suite of 5 new sulfonated BODIPYs with 2,6-disubstitution patterns spanning a rang

298 Spiro-BODIPYs with a diaryl chelate unit have been found to fo

299 The first series of arrays contains BODIPYs with PEG substituents attached to the boron, whe

300 Three furan fused boron dipyrromethenes (BODIPYs) with a CF3 group on the meso-carbon are synthes