-
1
-
-
79958839901
-
Benzotriazole-mediated syntheses of depsipeptides and oligoesters
-
10.1021/jo200174j 10.1021/jo200174j 1:CAS:528:DC%2BC3MXmsVeqsro%3D 21452874
-
Avan I, Tala SR, Steel PJ, Katritzky AR (2011) Benzotriazole-mediated syntheses of depsipeptides and oligoesters. J Org Chem 76:4884-4893. doi: 10.1021/jo200174j
-
(2011)
J Org Chem
, vol.76
, pp. 4884-4893
-
-
Avan, I.1
Tala, S.R.2
Steel, P.J.3
Katritzky, A.R.4
-
2
-
-
0036229133
-
Recent developments in depsipeptide research
-
10.2174/0929867023371049 1:CAS:528:DC%2BD38Xis1Olt70%3D 11945121
-
Ballard CE, Yu H, Wang B (2002) Recent developments in depsipeptide research. Curr Med Chem 9:471-498
-
(2002)
Curr Med Chem
, vol.9
, pp. 471-498
-
-
Ballard, C.E.1
Yu, H.2
Wang, B.3
-
3
-
-
43549085251
-
Surfactant-induced fluorescent sensor activity enhancement of tryptophan at various pH
-
10.1016/j.cplett.2008.03.076 10.1016/j.cplett.2008.03.076 1:CAS:528:DC%2BD1cXlvFyiur0%3D
-
Bandyopadhyay P, Saha K (2008) Surfactant-induced fluorescent sensor activity enhancement of tryptophan at various pH. Chem Phys Lett 457:227-231. doi: 10.1016/j.cplett.2008.03.076
-
(2008)
Chem Phys Lett
, vol.457
, pp. 227-231
-
-
Bandyopadhyay, P.1
Saha, K.2
-
4
-
-
4243106516
-
Environmental and magnetic field effects on exciplex and twisted charge transfer emission
-
10.1021/cr00017a022 10.1021/cr00017a022 1:CAS:528:DyaK3sXotVahtg%3D%3D
-
Bhattacharyya K, Chowdhury M (1993) Environmental and magnetic field effects on exciplex and twisted charge transfer emission. Chem Rev 93:507-535. doi: 10.1021/cr00017a022
-
(1993)
Chem Rev
, vol.93
, pp. 507-535
-
-
Bhattacharyya, K.1
Chowdhury, M.2
-
5
-
-
73649087584
-
On the mechanism of SDS-induced protein denaturation
-
10.1002/bip.21318 1:CAS:528:DC%2BD1MXhsVyls7jL 19802818
-
Bhuyan AK (2010) On the mechanism of SDS-induced protein denaturation. Biopolymers 93:186-199
-
(2010)
Biopolymers
, vol.93
, pp. 186-199
-
-
Bhuyan, A.K.1
-
6
-
-
0033549831
-
Total synthesis of quinoxapeptin A ± C: Establishment of absolute stereochemistry
-
10.1002/(SICI)1521-3773(19990816)38:16<2424: AID-ANIE2424>3.0.CO;2- 9 1:CAS:528:DyaK1MXls1Srs7w%3D
-
Boger DL, Ledeboer MW, Kume M (1999) Total synthesis of quinoxapeptin A ± C: establishment of absolute stereochemistry. Angew Chem Int Ed 38:2424-2426
-
(1999)
Angew Chem Int Ed
, vol.38
, pp. 2424-2426
-
-
Boger, D.L.1
Ledeboer, M.W.2
Kume, M.3
-
7
-
-
0017577685
-
Intramolecularly-quenched fluorescent peptides as fluorogenic substrates of leucine aminopeptidase and inhibitors of clostridial aminopeptidase
-
10.1111/j.1432-1033.1977.tb11357.x 10.1111/j.1432-1033.1977.tb11357.x 1:CAS:528:DyaE2sXhs1Kqurc%3D
-
Carmel A, Kessler E, Yaron A (1977) Intramolecularly-quenched fluorescent peptides as fluorogenic substrates of leucine aminopeptidase and inhibitors of clostridial aminopeptidase. Euro J Biochem 73:617-625. doi: 10.1111/j.1432-1033. 1977.tb11357.x
-
(1977)
Euro J Biochem
, vol.73
, pp. 617-625
-
-
Carmel, A.1
Kessler, E.2
Yaron, A.3
-
8
-
-
33845185140
-
Twisted internal charge transfer molecules: Already twisted in the ground state
-
10.1021/j100343a030 10.1021/j100343a030 1:CAS:528:DyaL1MXhtlCnsrg%3D
-
Cazeau-Dubroca C, Ait Lyazidi S, Cambou P et al (1989) Twisted internal charge transfer molecules: already twisted in the ground state. J Phys Chem 93:2347-2358. doi: 10.1021/j100343a030
-
(1989)
J Phys Chem
, vol.93
, pp. 2347-2358
-
-
Cazeau-Dubroca, C.1
Ait Lyazidi, S.2
Cambou, P.3
-
9
-
-
18744401100
-
Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase
-
10.1038/nmeth735 1:CAS:528:DC%2BD2MXisVGhsr4%3D
-
Chen I, Howarth M, Lin W, Ting AY (2005) Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase. Nat Method 2:99-104
-
(2005)
Nat Method
, vol.2
, pp. 99-104
-
-
Chen, I.1
Howarth, M.2
Lin, W.3
Ting, A.Y.4
-
10
-
-
79955422442
-
Design, synthesis, and pharmacological characterization of fluorescent peptides for imaging human V1b vasopressin or oxytocin receptors
-
10.1021/jm1016208 10.1021/jm1016208 1:CAS:528:DC%2BC3MXjsleqtL8%3D 21428295
-
Corbani M, Trueba M, Stoev S et al (2011) Design, synthesis, and pharmacological characterization of fluorescent peptides for imaging human V1b vasopressin or oxytocin receptors. J Med Chem 54:2864-2877. doi: 10.1021/jm1016208
-
(2011)
J Med Chem
, vol.54
, pp. 2864-2877
-
-
Corbani, M.1
Trueba, M.2
Stoev, S.3
-
11
-
-
80052843571
-
Photoionization and time-dependent stokes shift of coumarin 307 in soft matter: Solvation and radical-ion pair recombination dynamics
-
doi: 10.1021/jp203092c
-
Dhenadhayalan N, Selvaraju C, Ramamurthy P (2011) Photoionization and time-dependent stokes shift of coumarin 307 in soft matter: solvation and radical-ion pair recombination dynamics. J Phys Chem B 110829104346066. doi: 10.1021/jp203092c
-
(2011)
J Phys Chem B
, pp. 110829104346066
-
-
Dhenadhayalan, N.1
Selvaraju, C.2
Ramamurthy, P.3
-
12
-
-
34547602169
-
Chemical labeling of protein in living cells
-
10.1002/cbic.200700158 10.1002/cbic.200700158 1:CAS:528: DC%2BD2sXotlGhsLY%3D 17492742
-
Dragulescu-Andrasi A, Rao J (2007) Chemical labeling of protein in living cells. ChemBioChem 8:1099-1101. doi: 10.1002/cbic.200700158
-
(2007)
ChemBioChem
, vol.8
, pp. 1099-1101
-
-
Dragulescu-Andrasi, A.1
Rao, J.2
-
13
-
-
67650510671
-
Determinants of K + vs Na + Selectivity in Potassium Channels
-
10.1021/ja900168k 10.1021/ja900168k 1:CAS:528:DC%2BD1MXmtFKit78%3D 19456150
-
Dudev T, Lim C (2009) Determinants of K + vs Na + Selectivity in Potassium Channels. J Am Chem Soc 131:8092-8101. doi: 10.1021/ja900168k
-
(2009)
J Am Chem Soc
, vol.131
, pp. 8092-8101
-
-
Dudev, T.1
Lim, C.2
-
14
-
-
77955018405
-
Characterization of membrane protein non-native states. 2. The SDS-Unfolded States of Rhodopsin
-
10.1021/bi100339x 10.1021/bi100339x 1:CAS:528:DC%2BC3cXosFCmur0%3D 20575562
-
Dutta A, Kim T-Y, Moeller M et al (2010) Characterization of membrane protein non-native states. 2. The SDS-Unfolded States of Rhodopsin. Biochemistry 49:6329-6340. doi: 10.1021/bi100339x
-
(2010)
Biochemistry
, vol.49
, pp. 6329-6340
-
-
Dutta, A.1
Kim, T.-Y.2
Moeller, M.3
-
15
-
-
0037039882
-
Deactivation behavior and excited-state properties of (coumarin-4-yl)methyl derivatives. 2. Photocleavage of selected (coumarin-4-yl)methyl-caged adenosine cyclic 3',5'-monophosphates with fluorescence enhancement
-
10.1021/jo010692p 10.1021/jo010692p 1:CAS:528:DC%2BD38XjsFeksg%3D%3D 11856009
-
Eckardt T, Hagen V, Schade B et al (2002) Deactivation behavior and excited-state properties of (coumarin-4-yl)methyl derivatives. 2. Photocleavage of selected (coumarin-4-yl)methyl-caged adenosine cyclic 3',5'-monophosphates with fluorescence enhancement. J Org Chem 67:703-710. doi: 10.1021/jo010692p
-
(2002)
J Org Chem
, vol.67
, pp. 703-710
-
-
Eckardt, T.1
Hagen, V.2
Schade, B.3
-
16
-
-
23444451767
-
Critical micelle concentration of surfactants in aqueous buffered and unbuffered systems
-
10.1016/j.aca.2005.05.069 10.1016/j.aca.2005.05.069 1:CAS:528: DC%2BD2MXntVymsbY%3D
-
Fuguet E, Ràfols C, Rosés M, Bosch E (2005) Critical micelle concentration of surfactants in aqueous buffered and unbuffered systems. Anal Chim Acta 548:95-100. doi: 10.1016/j.aca.2005.05.069
-
(2005)
Anal Chim Acta
, vol.548
, pp. 95-100
-
-
Fuguet, E.1
Ràfols, C.2
Rosés, M.3
Bosch, E.4
-
17
-
-
0033574057
-
Brominated 7-hydroxycoumarin-4-ylmethyls: Photolabile protecting groups with biologically useful cross-sections for two photon photolysis
-
10.1073/pnas.96.4.1193 1:CAS:528:DyaK1MXhsFSrtrg%3D 9990000
-
Furuta T, Wang SS-H, Dantzker JL et al (1999) Brominated 7-hydroxycoumarin-4-ylmethyls: photolabile protecting groups with biologically useful cross-sections for two photon photolysis. Proc Natl Acad Sci USA 96:1193-1200
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 1193-1200
-
-
Furuta, T.1
Wang, S.-H.2
Dantzker, J.L.3
-
18
-
-
0000713034
-
Hydrogen-bond-mediated folding in depsipeptide models of.beta.-turns and.alpha.-helical turns
-
10.1021/ja00074a052 10.1021/ja00074a052 1:CAS:528:DyaK2cXjtFWruw%3D%3D
-
Gallo EA, Gellman SH (1993) Hydrogen-bond-mediated folding in depsipeptide models of.beta.-turns and.alpha.-helical turns. J Am Chem Soc 115:9774-9788. doi: 10.1021/ja00074a052
-
(1993)
J Am Chem Soc
, vol.115
, pp. 9774-9788
-
-
Gallo, E.A.1
Gellman, S.H.2
-
19
-
-
0032503999
-
Specific covalent labeling of recombinant protein molecules inside live cells
-
10.1126/science.281.5374.269 10.1126/science.281.5374.269 1:CAS:528:DyaK1cXksFKgs78%3D 9657724
-
Griffin B et al (1998) Specific covalent labeling of recombinant protein molecules inside live cells. Science 281:269-272. doi: 10.1126/science.281.5374. 269
-
(1998)
Science
, vol.281
, pp. 269-272
-
-
Griffin, B.1
-
20
-
-
33747100196
-
Hydrophilic photolabelling of glycopeptides from the murine liver-intestine (LI) cadherin recognition domain
-
10.1016/j.bmc.2006.06.014 10.1016/j.bmc.2006.06.014 1:CAS:528: DC%2BD28XosVOhsrs%3D 16828561
-
Heiner S, Detert H, Kuhn A, Kunz H (2006) Hydrophilic photolabelling of glycopeptides from the murine liver-intestine (LI) cadherin recognition domain. Bioorg Med Chem 14:6149-6164. doi: 10.1016/j.bmc.2006.06.014
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 6149-6164
-
-
Heiner, S.1
Detert, H.2
Kuhn, A.3
Kunz, H.4
-
21
-
-
0035909080
-
Incorporation of nonnatural amino acids into proteins by using various four-base codons in an escherichia coli in vitro translation system
-
10.1021/bi0108204 10.1021/bi0108204 1:CAS:528:DC%2BD3MXmtVWjur0%3D 11551202
-
Hohsaka T, Ashizuka Y, Taira H et al (2001) Incorporation of nonnatural amino acids into proteins by using various four-base codons in an escherichia coli in vitro translation system. Biochemistry 40:11060-11064. doi: 10.1021/bi0108204
-
(2001)
Biochemistry
, vol.40
, pp. 11060-11064
-
-
Hohsaka, T.1
Ashizuka, Y.2
Taira, H.3
-
22
-
-
0012248846
-
Solvent effects on emission yield and lifetime for coumarin laser dyes. Requirements for a rotatory decay mechanism
-
10.1021/j100248a024 10.1021/j100248a024 1:CAS:528:DyaL2MXltlaqsw%3D%3D
-
Jones G, Jackson WR, Choi CY, Bergmark WR (1985) Solvent effects on emission yield and lifetime for coumarin laser dyes. Requirements for a rotatory decay mechanism. J Phys Chem 89:294-300. doi: 10.1021/j100248a024
-
(1985)
J Phys Chem
, vol.89
, pp. 294-300
-
-
Jones, G.1
Jackson, W.R.2
Choi, C.Y.3
Bergmark, W.R.4
-
23
-
-
47349125605
-
Angrish P (2008a) chiral N-(coumarin-3-ylcarbonyl)-α-amino acids: Fluorescent markers for amino acids and dipeptides
-
10.1055/s-2008-1067078LA-EN
-
Katritzky AR, Narindoshvili T, Angrish P (2008a) Angrish P (2008a) chiral N-(coumarin-3-ylcarbonyl)-α-amino acids: fluorescent markers for amino acids and dipeptides. Synthesis 2013:2022. doi: 10.1055/s-2008-1067078LA-EN
-
(2008)
Synthesis
, vol.2013
, pp. 2022
-
-
Katritzky, A.R.1
Narindoshvili, T.2
Angrish, P.3
-
24
-
-
57049084769
-
Fluorescent labeling of peptides on solid phase
-
10.1039/b811693h 1:CAS:528:DC%2BD1cXhsVChtb7I 19039367
-
Katritzky AR, Yoshioka M, Narindoshvili T et al (2008b) Fluorescent labeling of peptides on solid phase. Org Biomol Chem 6:4582-4586
-
(2008)
Org Biomol Chem
, vol.6
, pp. 4582-4586
-
-
Katritzky, A.R.1
Yoshioka, M.2
Narindoshvili, T.3
-
25
-
-
78650521336
-
Novel fluorescent aminoxy acids and aminoxy hybrid peptides
-
10.1055/s-0030-1258345 10.1055/s-0029-1220012
-
Katritzky A, Abdelmajeid A, Tala S et al (2010) Novel fluorescent aminoxy acids and aminoxy hybrid peptides. Synthesis 2010:83-90. doi: 10.1055/s-0030-1258345
-
(2010)
Synthesis
, vol.2010
, pp. 83-90
-
-
Katritzky, A.1
Abdelmajeid, A.2
Tala, S.3
-
26
-
-
65349097586
-
Tubulin-interactive natural products as anticancer agents(1)
-
10.1021/np800568j 10.1021/np800568j 1:CAS:528:DC%2BD1MXktVOmsQ%3D%3D 19125622
-
Kingston DGI (2009) Tubulin-interactive natural products as anticancer agents(1). J Nat Prod 72:507-515. doi: 10.1021/np800568j
-
(2009)
J Nat Prod
, vol.72
, pp. 507-515
-
-
Kingston, D.G.I.1
-
27
-
-
0026505650
-
A novel coumarin-labelled peptide for sensitive continuous assays of the matrix metalloproteinases
-
10.1016/0014-5793(92)80300-6 1:CAS:528:DyaK38XitlSnu7Y%3D 1537400
-
Knight CG, Willenbrock F, Murphy G (1992) A novel coumarin-labelled peptide for sensitive continuous assays of the matrix metalloproteinases. FEBS Lett 296:263-266
-
(1992)
FEBS Lett
, vol.296
, pp. 263-266
-
-
Knight, C.G.1
Willenbrock, F.2
Murphy, G.3
-
28
-
-
0000363049
-
Effect of micelles on dual fluorescence of 2-(4′-N, N-dimethylaminophenyl)pyrido[3,4-d]imidazole
-
10.1016/S0009-2614(00)00511-X 1:CAS:528:DC%2BD3cXktVShtL0%3D
-
Krishnamoorthy G, Dogra SK (2000) Effect of micelles on dual fluorescence of 2-(4′-N, N-dimethylaminophenyl)pyrido[3,4-d]imidazole. Chem Phys Lett 323:234-242
-
(2000)
Chem Phys Lett
, vol.323
, pp. 234-242
-
-
Krishnamoorthy, G.1
Dogra, S.K.2
-
29
-
-
0344241060
-
A general methodology for automated solid-phase synthesis of depsides and depsipeptides. preparation of a valinomycin analogue
-
10.1021/jo981580 10.1021/jo981580+ 1:CAS:528:DyaK1MXmt12lurY%3D 11674717
-
Kuisle O, Quiñoá E, Riguera R (1999) A general methodology for automated solid-phase synthesis of depsides and depsipeptides. preparation of a valinomycin analogue. J Org Chem 64:8063-8075. doi: 10.1021/jo981580
-
(1999)
J Org Chem
, vol.64
, pp. 8063-8075
-
-
Kuisle, O.1
Quiñoá, E.2
Riguera, R.3
-
30
-
-
79952296066
-
Mirabamides e - H, HIV-inhibitory depsipeptides from the sponge stelletta clavosa
-
10.1021/np100613p 10.1021/np100613p 1:CAS:528:DC%2BC3MXhsVSit7o%3D 21280591
-
Lu Z, Van Wagoner RM, Harper MK et al (2011) Mirabamides E - H, HIV-inhibitory depsipeptides from the sponge stelletta clavosa. J Nat Prod 74:185-193. doi: 10.1021/np100613p
-
(2011)
J Nat Prod
, vol.74
, pp. 185-193
-
-
Lu, Z.1
Van Wagoner, R.M.2
Harper, M.K.3
-
31
-
-
19944422124
-
Shape and position of 4-aminophthalimide (4-AP) time-resolved emission spectra (TRES) versus sodium dodecyl sulfate SDS concentration in micellar solutions: The partitioning of 4-AP in the micellar phase and in water surrounding the micelles
-
10.1021/jp044097d 10.1021/jp044097d 1:CAS:528:DC%2BD2MXjt1SksLg%3D 16852130
-
Maciejewski A, Kubicki J, Dobek K (2005) Shape and position of 4-aminophthalimide (4-AP) time-resolved emission spectra (TRES) versus sodium dodecyl sulfate SDS concentration in micellar solutions: the partitioning of 4-AP in the micellar phase and in water surrounding the micelles. J Phys Chem B 109:9422-9431. doi: 10.1021/jp044097d
-
(2005)
J Phys Chem B
, vol.109
, pp. 9422-9431
-
-
Maciejewski, A.1
Kubicki, J.2
Dobek, K.3
-
32
-
-
0346540824
-
AM1 study of the electronic structure of coumarins
-
10.1021/j100149a018 10.1021/j100149a018 1:CAS:528:DyaK3sXmslSnurc%3D
-
McCarthy PK, Blanchard GJ (1993) AM1 study of the electronic structure of coumarins. J Phys Chem 97:12205-12209. doi: 10.1021/j100149a018
-
(1993)
J Phys Chem
, vol.97
, pp. 12205-12209
-
-
McCarthy, P.K.1
Blanchard, G.J.2
-
33
-
-
9644291609
-
Interaction of Lucifer yellow with cetyltrimethyl ammonium bromide micelles and the consequent suppression of its non-radiative processes
-
10.1016/j.cplett.2004.10.101 10.1016/j.cplett.2004.10.101 1:CAS:528:DC%2BD2cXhtVaku7vL
-
Mishra PP, Koner AL, Datta A (2004) Interaction of Lucifer yellow with cetyltrimethyl ammonium bromide micelles and the consequent suppression of its non-radiative processes. Chem Phys Lett 400:128-132. doi: 10.1016/j.cplett.2004. 10.101
-
(2004)
Chem Phys Lett
, vol.400
, pp. 128-132
-
-
Mishra, P.P.1
Koner, A.L.2
Datta, A.3
-
34
-
-
84985609328
-
Charge separation in excited states of decoupled systems - TICT compounds and implications regarding the development of new laser dyes and the primary process of vision and photosynthesis
-
10.1002/anie.198609711
-
Rettig W (1986) Charge separation in excited states of decoupled systems - TICT compounds and implications regarding the development of new laser dyes and the primary process of vision and photosynthesis. Angew Chem Int Ed Engl 25:971-988
-
(1986)
Angew Chem Int Ed Engl
, vol.25
, pp. 971-988
-
-
Rettig, W.1
-
35
-
-
0034270368
-
Excited-state dipole moment of 7-aminocoumarins as determined from time-resolved microwave dielectric absorption measurements
-
10.1021/jp001676j 10.1021/jp001676j 1:CAS:528:DC%2BD3cXlslCht7s%3D
-
Samanta A, Fessenden RW (2000) Excited-state dipole moment of 7-aminocoumarins as determined from time-resolved microwave dielectric absorption measurements. J Phys Chem A 104:8577-8582. doi: 10.1021/jp001676j
-
(2000)
J Phys Chem A
, vol.104
, pp. 8577-8582
-
-
Samanta, A.1
Fessenden, R.W.2
-
36
-
-
33748392395
-
Solvation dynamics of coumarin 480 in micelles
-
10.1021/jp960630g 10.1021/jp960630g 1:CAS:528:DyaK28Xlt1OmsLo%3D
-
Sarkar N, Datta A, Das S, Bhattacharyya K (1996) Solvation dynamics of coumarin 480 in micelles. J Phys Chem 100:15483-15486. doi: 10.1021/jp960630g
-
(1996)
J Phys Chem
, vol.100
, pp. 15483-15486
-
-
Sarkar, N.1
Datta, A.2
Das, S.3
Bhattacharyya, K.4
-
37
-
-
35349013121
-
Amide-to-ester substitution in coiled coils: The effect of removing hydrogen bonds on protein structure
-
10.1002/anie.200702218 10.1002/anie.200702218 1:CAS:528: DC%2BD2sXht1alsL3N 17876795
-
Scheike JA, Baldauf C, Spengler J et al (2007) Amide-to-ester substitution in coiled coils: the effect of removing hydrogen bonds on protein structure. Angew Chem Int Ed Engl 46:7766-7769. doi: 10.1002/anie.200702218
-
(2007)
Angew Chem Int Ed Engl
, vol.46
, pp. 7766-7769
-
-
Scheike, J.A.1
Baldauf, C.2
Spengler, J.3
-
38
-
-
0016925901
-
New laser dyes with blue-green emission
-
10.1016/0030-4018(76)90005-5 1:CAS:528:DyaE28Xht1ymsbs%3D
-
Schimitschek EJ, Trias JA, Hammond PR et al (1976) New laser dyes with blue-green emission. Opt Commun 16:313-316
-
(1976)
Opt Commun
, vol.16
, pp. 313-316
-
-
Schimitschek, E.J.1
Trias, J.A.2
Hammond, P.R.3
-
39
-
-
4644249283
-
Photophysical properties of coumarin-30 dye in aprotic and protic solvents of varying polarities
-
10.1562/2004-03-19-RA-119.1 1:CAS:528:DC%2BD2cXnsVeisrs%3D 15339222
-
Senthilkumar S, Nath S, Pal H (2004) Photophysical properties of coumarin-30 dye in aprotic and protic solvents of varying polarities. Photochem Photobiol 80:104-111
-
(2004)
Photochem Photobiol
, vol.80
, pp. 104-111
-
-
Senthilkumar, S.1
Nath, S.2
Pal, H.3
-
40
-
-
2342522662
-
Dynamic fluorescence probing of the microenvironment of sodium dodecyl sulfate micelle solutions: Surfactant concentration dependence and solvent isotope effect
-
10.1021/jp035861j 10.1021/jp035861j 1:CAS:528:DC%2BD2cXitFyisLY%3D
-
Shirota H, Tamoto Y, Segawa H (2004) Dynamic fluorescence probing of the microenvironment of sodium dodecyl sulfate micelle solutions: surfactant concentration dependence and solvent isotope effect. J Phys Chem A 108:3244-3252. doi: 10.1021/jp035861j
-
(2004)
J Phys Chem A
, vol.108
, pp. 3244-3252
-
-
Shirota, H.1
Tamoto, Y.2
Segawa, H.3
-
41
-
-
0029114876
-
Mechanism of protein synthesis inhibition by Didemnin B in vitro
-
10.1021/bi00028a030 10.1021/bi00028a030 1:CAS:528:DyaK2MXmsFejurw%3D 7619818
-
SirDeshpande BV, Toogood PL (1995) Mechanism of protein synthesis inhibition by Didemnin B in vitro. Biochemistry 34:9177-9184. doi: 10.1021/bi00028a030
-
(1995)
Biochemistry
, vol.34
, pp. 9177-9184
-
-
Sirdeshpande, B.V.1
Toogood, P.L.2
-
42
-
-
84863011769
-
Integrated SDS removal and peptide separation by strong-cation exchange liquid chromatography for SDS-assisted shotgun proteome analysis
-
10.1021/pr200676v 10.1021/pr200676v 1:CAS:528:DC%2BC38Xht1eqsA%3D%3D
-
Sun D, Wang N, Li L (2012) Integrated SDS removal and peptide separation by strong-cation exchange liquid chromatography for SDS-assisted shotgun proteome analysis. J Proteom Res 11:818-828. doi: 10.1021/pr200676v
-
(2012)
J Proteom Res
, vol.11
, pp. 818-828
-
-
Sun, D.1
Wang, N.2
Li, L.3
-
43
-
-
79952899655
-
Construction of a more sensitive fluorescence sensing material for the detection of vascular endothelial growth factor, a biomarker for angiogenesis, prepared by combining a fluorescent peptide and a nanopillar substrate
-
10.1016/j.bios.2011.02.007 10.1016/j.bios.2011.02.007 1:CAS:528:DC%2BC3MXjvFeitrY%3D 21388797
-
Suzuki Y, Yokoyama K (2011) Construction of a more sensitive fluorescence sensing material for the detection of vascular endothelial growth factor, a biomarker for angiogenesis, prepared by combining a fluorescent peptide and a nanopillar substrate. Biosens Bioelectron 26:3696-3699. doi: 10.1016/j.bios.2011.02.007
-
(2011)
Biosens Bioelectron
, vol.26
, pp. 3696-3699
-
-
Suzuki, Y.1
Yokoyama, K.2
-
44
-
-
49549144734
-
Application of a generating function to reaction kinetics in micelles. Kinetics of quenching of luminescent probes in micelles
-
10.1016/0009-2614(75)80158-8 1:CAS:528:DyaE2MXkvVyjsrs%3D
-
Tachiya M (1975) Application of a generating function to reaction kinetics in micelles. Kinetics of quenching of luminescent probes in micelles. Chem Phys Lett 33:289-292
-
(1975)
Chem Phys Lett
, vol.33
, pp. 289-292
-
-
Tachiya, M.1
-
45
-
-
0034106843
-
Structuarl features for fluorescing present in methoxycoumarin derivatives
-
10.1248/cpb.48.256 1:CAS:528:DC%2BD3cXhtVSisbc%3D 10705514
-
Takadate A, Masuda T, Murata C et al (2000) Structuarl features for fluorescing present in methoxycoumarin derivatives. Chem Pharm Bull 48:256-260
-
(2000)
Chem Pharm Bull
, vol.48
, pp. 256-260
-
-
Takadate, A.1
Masuda, T.2
Murata, C.3
-
46
-
-
73149116645
-
SDS micelles as a membrane-mimetic environment for transmembrane segments
-
10.1021/bi9013819 10.1021/bi9013819 1:CAS:528:DC%2BD1MXhsVyjt7fI 19921933
-
Tulumello DV, Deber CM (2009) SDS micelles as a membrane-mimetic environment for transmembrane segments. Biochemistry 48:12096-12103. doi: 10.1021/bi9013819
-
(2009)
Biochemistry
, vol.48
, pp. 12096-12103
-
-
Tulumello, D.V.1
Deber, C.M.2
-
47
-
-
58949096544
-
The use of coumarins as environmentally-sensitive fluorescent probes of heterogeneous inclusion systems
-
10.3390/molecules14010210 10.3390/molecules14010210 1:CAS:528: DC%2BD1MXht1Slsbk%3D 19127249
-
Wagner BD (2009) The use of coumarins as environmentally-sensitive fluorescent probes of heterogeneous inclusion systems. Molecules 14:210-237. doi: 10.3390/molecules14010210
-
(2009)
Molecules
, vol.14
, pp. 210-237
-
-
Wagner, B.D.1
-
48
-
-
54349118620
-
Synthesis and application of dipeptides; Current status and perspectives
-
10.1007/s00253-008-1590-3 10.1007/s00253-008-1590-3 1:CAS:528: DC%2BD1cXht1Oisb3F 18795289
-
Yagasaki M, Hashimoto S (2008) Synthesis and application of dipeptides; current status and perspectives. Appl Microbiol Biotechnol 81:13-22. doi: 10.1007/s00253-008-1590-3
-
(2008)
Appl Microbiol Biotechnol
, vol.81
, pp. 13-22
-
-
Yagasaki, M.1
Hashimoto, S.2
-
49
-
-
0032500312
-
Energetic superiority of two-center hydrogen bonding relative to three-center hydrogen bonding in a model system
-
10.1021/ja981604u
-
Yang J, Gellman SH (1998) Energetic superiority of two-center hydrogen bonding relative to three-center hydrogen bonding in a model system. J Am Chem Soc 7863:9090-9091
-
(1998)
J Am Chem Soc
, vol.7863
, pp. 9090-9091
-
-
Yang, J.1
Gellman, S.H.2
-
50
-
-
0032790483
-
Characterization of new fluorogenic substrates for the rapid and sensitive assay of cathepsin e and cathepsin D
-
10.1093/oxfordjournals.jbchem.a022396 1:CAS:528:DyaK1MXlsVygsr4%3D 10348917
-
Yasuda Y, Kageyama T, Akamine A et al (1999) Characterization of new fluorogenic substrates for the rapid and sensitive assay of cathepsin E and cathepsin D. J Biochem 125:1137-1143
-
(1999)
J Biochem
, vol.125
, pp. 1137-1143
-
-
Yasuda, Y.1
Kageyama, T.2
Akamine, A.3
-
51
-
-
0030037593
-
Callipeltin A, an anti-HIV cyclic depsipeptide from the new caledonian lithistida sponge callipelta sp
-
10.1021/ja954287p 10.1021/ja954287p 1:CAS:528:DyaK28XjsFequ7w%3D
-
Zampella A, D'Auria MV, Paloma LG et al (1996) Callipeltin A, an anti-HIV cyclic depsipeptide from the new caledonian lithistida sponge callipelta sp. J Am Chem Soc 118:6202-6209. doi: 10.1021/ja954287p
-
(1996)
J Am Chem Soc
, vol.118
, pp. 6202-6209
-
-
Zampella, A.1
D'Auria, M.V.2
Paloma, L.G.3
-
52
-
-
3242811187
-
A Fluorogenic probe for the copper (I) -catalyzed azide-alkyne ligation reaction: Modulation of the fluorescence emission via 3 (n, π) - 1 (π, π) inversion
-
10.1021/ja049684r
-
Zhou Z, Fahrni CJ (2004) A Fluorogenic probe for the copper (I) -catalyzed azide-alkyne ligation reaction: modulation of the fluorescence emission via 3 (n, π) - 1 (π, π) inversion. J Am Chem Soc 3:8862-8863
-
(2004)
J Am Chem Soc
, vol.3
, pp. 8862-8863
-
-
Zhou, Z.1
Fahrni, C.J.2
|