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1 optical fine-tuning of meso-aryl-substituted bacteriochlorins.
2 nd contrasted against benchmark chlorins and bacteriochlorins.
3 rted concerning the synthesis of substituted bacteriochlorins.
4 nce the capabilities for tailoring synthetic bacteriochlorins.
5  agents within the optical window of tissue, bacteriochlorins (2,3,12,13-tetrahydroporphyrins) promis
6                                              Bacteriochlorin 26 under acidic or basic conditions main
7 ring a 1,3-dioxolan-2-yl moiety afforded the bacteriochlorin (30% yield) containing a 2-hydroxyethoxy
8 rins and 13(1)-oxophorbines (603-687 nm) and bacteriochlorins (707-792 nm).
9                                         Each bacteriochlorin acceptor is equipped with a different se
10 results in relatively strong emission of the bacteriochlorin acceptor, with a quantum yield Phif rang
11                            Interestingly all bacteriochlorins accumulate in melanosomes, and subseque
12             Zinc and copper chelates of each bacteriochlorin also were prepared.
13                                              Bacteriochlorin analogue BC-PMI has more extended spectr
14  prepared and oxidatively stable chlorin and bacteriochlorin analogues with tunable optical spectra t
15 electronic structure of a family of expanded bacteriochlorin analogues.
16 a readily separable mixture of two free base bacteriochlorins and a free base B,D-tetradehydrocorrin.
17 -harvesting porphyrins, chlorins, and mainly bacteriochlorins and are also known for being efficient
18      Di- and tetrahydroporphyrins (chlorins, bacteriochlorins and isobacteriochlorins, respectively)
19      In summary, this simple entry to stable bacteriochlorins and tetradehydrocorrins should facilita
20  comprising a near-IR absorbing and emitting bacteriochlorin, and BODIPY derivatives with different a
21      The optical properties of the chlorin-, bacteriochlorin-, and isobacteriochlorin-type chromophor
22 ent strengths of the porphins, chlorins, and bacteriochlorins are 1.5-2.5 times stronger than for ben
23    The current strengths of the chlorins and bacteriochlorins are 19-24 nA/T depending on whether the
24                                              Bacteriochlorins are attractive candidates for a wide va
25                                              Bacteriochlorins are attractive candidates for photodyna
26 operties of mono- and bis-chromene-annulated bacteriochlorins are described.
27 ctra of the mono- and bis-chromene-annulated bacteriochlorins are modulated as a result of the annula
28                                    Synthetic bacteriochlorins are of interest for fundamental studies
29 exciting results, we believe that platinated bacteriochlorins are promising candidates for further in
30         Cell killing studies determined that bacteriochlorins are superior at (LD(50) approximately 0
31                                              Bacteriochlorins are tetrapyrrole compounds with two red
32 , with absorption between 500-700 nm, BODIPY-bacteriochlorin arrays should allow for construction of
33 ergy donor, and a different near-IR emitting bacteriochlorin, as an energy acceptor.
34 (HPPH) and structurally related chlorins and bacteriochlorins at different positions of the tetrapyrr
35  of peripheral functional groups makes these bacteriochlorins attractive candidates for diverse appli
36 e report an innovative approach to producing bacteriochlorins (bacs) via formal cycloaddition by subj
37             Herein we report the design of a bacteriochlorin-based nanoscale metal-organic framework,
38 ion of a free-base chlorin generally forms a bacteriochlorin (BC), while the reduction of the corresp
39 inated chromophores, which include synthetic bacteriochlorins (BC1, BC2) with strong near-infrared ab
40                                   The target bacteriochlorins bear cationic, lipophilic, or amphipath
41                                      Ten new bacteriochlorins bearing 0-6 total aryl, alkyl, and carb
42 , Sonogashira, Hartwig-Buchwald) to give six bacteriochlorins bearing functional groups at the 15-pos
43                                     Five new bacteriochlorins bearing various substituents (alkyl/alk
44 , the characteristic absorbance bands of the bacteriochlorins bound to the polypeptides within the re
45 at the 15-position to give a trans-(5,15)-AB-bacteriochlorin building block.
46 rins are thus excellent models for localized bacteriochlorin chromophore deformations that are sugges
47  of the modulation is due to ruffling of the bacteriochlorin chromophore.
48 s vary the tetrapyrrole (porphyrin, chlorin, bacteriochlorin), chromophore (boron-dipyrrin, perylene,
49                                              Bacteriochlorins containing anhydride, imide, or isoimid
50                                    Synthetic bacteriochlorins containing site-specific isotopic subst
51                                         Each bacteriochlorin contains two geminal dimethyl groups to
52        The absorption spectra of these novel bacteriochlorins demonstrated remarkably red-shifted int
53                                          The bacteriochlorins display characteristic spectral feature
54 , which in case of the 13-13' ethynyl-linked bacteriochlorin dyad is positioned past 800 nm.
55                                              Bacteriochlorin dyads exhibit a strong dependence of flu
56  and split for the 13-13' linked chlorin and bacteriochlorin dyads.
57 nediyne linker in hydroporphyrin (chlorin or bacteriochlorin) dyads leads to thermally stable cis iso
58 ongly conjugated hydroporphyrin (chlorin and bacteriochlorin) dyads.
59 id catalysis conditions has afforded diverse bacteriochlorins (e.g., bearing alkyl/ester, aryl/ester,
60         The narrow, tunable emission band of bacteriochlorins enables the selection of a series of th
61 ical properties of a series of novel chlorin-bacteriochlorin energy transfer dyads are described.
62                                          The bacteriochlorins exhibit absorption spectra typical of b
63                                          The bacteriochlorins exhibit characteristic bacteriochloroph
64                                         Each bacteriochlorin exhibits a Q(y) absorption band in the r
65 r, this study expands the scope of available bacteriochlorins for fundamental studies and diverse app
66 describes testing of 12 new stable synthetic bacteriochlorins for PDT activity.
67 nge between 4 A to 11 A and that between two bacteriochlorins from different subunits is more than 20
68 er with near-infrared absorption gives these bacteriochlorins great potential as photosensitizers for
69                   Deuterium exchange of both bacteriochlorins (H-BC and MeO-BC) in acidic media (TFA-
70                      Altogether 22 free base bacteriochlorins have been prepared.
71 teriochlorin (MeOBC-type), a 5-unsubstituted bacteriochlorin (HBC-type), and a free base B,D-tetradeh
72 s two geminal dimethyl groups to lock-in the bacteriochlorin hydrogenation level, p-tolyl substituent
73 nsequently (3) access to diverse substituted bacteriochlorins including those with substituents at th
74                                         Each bacteriochlorin is stable to adventitious dehydrogenatio
75 of a bis-chromene-annulated chlorin from the bacteriochlorins is also described, including its X-ray
76 -tune the electronic properties of synthetic bacteriochlorins is important for these purposes.
77                             Together, the 24 bacteriochlorin isotopologues should provide valuable be
78                             By contrast, the bacteriochlorin lacking the 5-methoxy group (8,8,18,18-t
79 hereby maintaining an 18-atom 18-pi electron bacteriochlorin-like aromatic delocalization pathway.
80 ned and up to 90 nm bathochromically shifted bacteriochlorin-like optical spectra.
81 d dioxabacteriochlorins may have chlorin- or bacteriochlorin-like spectra.
82  Microscopy reveals that the least effective bacteriochlorin localizes predominantly in lysosomes, wh
83               Bacteriochlorophylls contain a bacteriochlorin macrocycle bearing an annulated fifth ri
84  unit attached to pyrroline ring B forms the bacteriochlorin macrocycle, and (ii) Nazarov cyclization
85 manifested by nearly exclusive emission from bacteriochlorin moiety upon BODIPY excitation.
86 parable with that observed for corresponding bacteriochlorin monomer, and is significantly reduced in
87                                    The novel bacteriochlorins, obtained from chlorophyll-a, have long
88 dination chemistry (e.g., Zn, Cd, Ni), (2) a bacteriochlorin oxidation state of the macrocyclic ring,
89 t energy transfer (>/=0.77) even for chlorin-bacteriochlorin pairs with large (up to 122 nm) separati
90 ers of redaporfin (a fluorinated sulfonamide bacteriochlorin photosensitizer of 1135 Da) are separabl
91                                   The 15 new bacteriochlorins prepared herein exhibit a long-waveleng
92 orescent probes show that the most effective bacteriochlorin produces significantly higher levels of
93 es of the isolated porphyrins, chlorins, and bacteriochlorins, related to Bchl a, were assigned on th
94 ds between LH2 alphabeta-side chains and the bacteriochlorin rings, further emphasizing the major rol
95                                          The bacteriochlorins show relatively low fluorescence quantu
96 pared from commercially available reactants (bacteriochlorin sites): ((13)C)paraformaldehyde (1, 11);
97 tes different sets of bis-chromene-annulated bacteriochlorin stereo- and regioisomers.
98 of synthetic plans for early installation of bacteriochlorin substituents via the dihydrodipyrrin-ace
99  differ in the levels of pigmentation; 3 new bacteriochlorins successfully overcame the resistance.
100            The distances between neighboring bacteriochlorin systems within a subunit range between 4
101 r-TBB stabilizes 5,10,15,20-tetra(p-benzoato)bacteriochlorin (TBB) ligands toward oxygen and light vi
102                                              Bacteriochlorins (tetrahydroporphyrins) are attractive f
103 gree of reduction is significantly lower for bacteriochlorins than for Photofrin.
104 single-isotopic substitution gives rise to a bacteriochlorin that contains two isotopic substitutions
105  may provide simple strategies for designing bacteriochlorins that efficiently generate ROS upon phot
106                                Among all the bacteriochlorins the triplet states were quenched by gro
107  groups at a specific site enables synthetic bacteriochlorins to be tailored for a variety of applica
108 ect of indocyanine green, Photodithazine(R), bacteriochlorin-trizma, and protoporphyrin IX against St
109 ties is described, generating inter alia the bacteriochlorin-type chromophores oxazolobacteriochlorin
110                                          The bacteriochlorin-type optical spectra of the mono- and bi
111          The first examples of bis-modified, bacteriochlorin-type PMPs containing either two eight-me
112  formation of the dihydrodipyrrin-acetal and bacteriochlorin underpins evaluation of synthetic plans
113                               A new route to bacteriochlorins via Northern-Southern (N-S) self-conden
114 a building block in the synthesis of diverse bacteriochlorins via Pd-mediated coupling reactions (Son
115                                         Each bacteriochlorin was prepared in five steps from an alpha
116                 The best in vitro performing bacteriochlorin was tested in vivo in a mouse melanoma m
117                              A series of new bacteriochlorins was synthesized using 13(2)-oxo-bacteri
118 rties, and skin phototoxicity of some stable bacteriochlorins were investigated.
119 ining PEG-substituted BODIPY and chlorins or bacteriochlorins were prepared and their optical and flu
120          Eight such isotopically substituted bacteriochlorins were prepared from commercially availab
121 tal X-ray structures (two intermediates, two bacteriochlorins) were determined.
122  novo synthesis has been employed to prepare bacteriochlorins wherein each macrocycle contains a pair
123 ring with KOH/propanol produced an "unstable bacteriochlorin", which decomposed in acidic conditions
124 rein, we report stable conjugates of a novel bacteriochlorin with cisplatin and transplatin.
125 thalene afforded highly conjugated annulated bacteriochlorins with fused quinoxaline, benzimidazole,

 
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