共查询到20条相似文献,搜索用时 31 毫秒
1.
Morais M Raposinho PD Oliveira MC Correia JD Santos I 《Journal of biological inorganic chemistry》2012,17(4):491-505
Abstract
Aiming to apply the multivalency concept to melanoma imaging, we have assessed the in vivo melanocortin type 1 receptor (MC1R)-targeting properties of 99mTc(I)-labeled homobivalent peptide conjugates which contain copies of the α-melanocyte-stimulating hormone (α-MSH) analog [Ac-Nle4, Asp5, d-Phe7, Lys11]α-MSH4–11 separated by linkers of different length (L 2 nine atoms and L 3 14 atoms). The MC1R-binding affinity of L 2 and L 3 is significantly higher than that of the monovalent conjugate L 1 . Metallation of these conjugates yielded the complexes fac-[M(CO)3(k3-L)]+ (M is 99mTc/Re; 1/1a, L is L 1 ; 2/2a, L is L 2 ; 3/3a, L is L 3 ), with IC50 values in the subnanomolar and nanomolar range. The MC1R-mediated internalization of 2 and 3 is higher than that of 1 in B16F1 melanoma cells. Biodistribution studies in melanoma-bearing mice have shown low nonspecific accumulation with a tumor uptake that correlates with IC50 values. However, no correlation between tumor uptake and valency was found. Nevertheless, 2 displayed the highest tumor retention, and the best tumor to nontarget organ ratios. 相似文献2.
《Journal of receptor and signal transduction research》2013,33(1-4):421-430
ABSTRACTThe coat colour in mammals is determined by the relative amounts of eumelanin (black/brown) and phaeomelanin (red/yellow), produced in melanocytes, which are controlled by melanocyte stimulating hormone receptor (MSH-R). Melanocyte stimulating hormone receptor is activated by α-melanocyte-stimulating hormone (α-MSH). Stimulated MSH-R activates adenylyl cyclase (AC), thereby increasing the amount of cyclic AMP in the cell, which activates the enzyme tyrosinase resulting in eumelanin synthesis. In this study the complete coding sequences of five alleles of the MSH-R gene found in Holstein, Red Holstein, Simmental, and Brown Swiss cattle were cloned into a mammalian expression vector and transfected into human embryonic kidney (HEK) 293 cells. The expressed receptors were analyzed for their ability to increase intracellular cAMP in response to stimulation by α-MSH. The recessive red allele (e) found in Red Holstein and Simmental and the dominant black allele (ED) found in Holstein were unresponsive to a wide range of α-MSH concentrations. Two alleles from Brown Swiss (Ed1, Ed2) and one allele found in the Simmental breed (ef) responded to stimulation by α-MSH in a dose-dependent manner. When compared to Ed1 and Ed2, the cells transfected with the ef MSH-R allele, however, reached the corresponding intracellular cAMP concentrations at a 10-fold higher concentration of α-MSH. In conjunction with the mode of inheritance of coat colour, the results indicate that the e MSH-R allele is a non-functional receptor, ED is constitutively activated receptor, and Ed1 and Ed2 are hormonally activated receptors. The delay in ef MSH-R response may explain the similarity between the e and ef phenotypes. 相似文献
3.
Ramirededy Nageswara Reddy Ravichandra Reddy Mutyala Polamarasetty Aparoy Pallu Reddanna Mutyala Rami Reddy 《Journal of molecular modeling》2010,16(2):203-209
Since the human body for many reasons can adapt and become resistant to drugs, it is important to develop and validate computer
aided drug design (CADD) methods that could help predict binding affinity changes that can result from these resistant enzymes.
The free energy perturbation (FEP) methodology is the most accurate means of estimating relative binding affinities between
inhibitors and protein variants. In this paper, we describe the role played by hydrophobic residues lining the active site
region, particularly
79
Ile and
176
Phe, in the binding of methotrexate to the Escherichia coli (E. coli) thymidylate synthase (TS) enzyme, using the thermodynamic cycle perturbation (TCP) approach. The computed binding free energy
differences on the binding of methotrexate to the native and some mutant E. coli TS structures have been compared with experimental results. Computationally, four different ‘mutations’ have been simulated
on the TS enzyme with methotrexate (MTX):
79
Ile →
79
Val;
79
Ile →
79
Ala;
79
Ile →
79
Leu; and
176
Phe →
176
Ile. The calculated results indicate that in each of these cases, the native residues (
79
Ile and
176
Phe) interact more favorably with methotrexate than the mutant residues and these results are corroborated by experimental measurements.
Binding preference to wild type residues can be rationalized in terms of their better hydrophobic contacts with the phenyl
ring of methotrexate. 相似文献
4.
Plant regeneration from mesophyll protoplasts of pepper,Capsicum annuum
L. cv. California Wonder has been demonstrated via shoot organogenesis. Protoplasts isolated from fully expanded leaves of
3-week-old axenic shoots when cultured in TM medium supplemented with 1 mg l
−1
NAA, 1 mg l
−1
2,4-D, 0 5 mg l
−1
BAP (CM 1) resulted in divisions with a frequency ranging from 20–25 %. Antioxidant ascorbic acid and polyvinylpyrrolidone
(PVP) in the medium and incubation in the dark helped overcome browning of protoplasts. Microcalli and macrocalli were formed
in TM medium containing 2 mg l
−1
NAA and 0.5 mg l
−1
BAP (CM II) and MS gelled medium containing 2 mg 1
−1
NAA and 0 5 mg 1
−1
BAP (CM III), respectively. Regeneration of plantlets was possible via caulogenesis. Microshoots, 2–5 percallus appeared on
MS gelled medium enriched with 0.5 mg l
−1
IAA, 2mg l
−1
GA and l0mg l
−1
BAP (CM IVc). Rooting of microshoots was obtained on half strength gelled medium containing 1 mg l
−1
NAA and 0.5mg l
−1
BAP. Protoplasts isolated from cotyledons failed to divide and degenerated eventually. 相似文献
5.
Lukas K. Filak Gerhard Mühlgassner Michael A. Jakupec Petra Heffeter Walter Berger Vladimir B. Arion Bernhard K. Keppler 《Journal of biological inorganic chemistry》2010,15(6):903-918
The synthesis of ruthenium(II) and osmium(II) arene complexes with the closely related indolo[3,2-c]quinolines N-(11H-indolo[3,2-c]quinolin-6-yl)-ethane-1,2-diamine (L
1
) and N′-(11H-indolo[3,2-c]quinolin-6-yl)-N,N-dimethylethane-1,2-diamine (L
2
) and indolo[3,2-d]benzazepines N-(7,12-dihydroindolo-[3,2-d][1]benzazepin-6-yl)-ethane-1,2-diamine (L
3
) and N′-(7,12-dihydroindolo-[3,2-d][1]benzazepin-6-yl)-N,N-dimethylethane-1,2-diamine (L
4
) of the general formulas [(η6-p-cymene)MII(L
1
)Cl]Cl, where M is Ru (4) and Os (6), [(η6-p-cymene)MII(L
2
)Cl]Cl, where M is Ru (5) and Os (7), [(η6-p-cymene)MII(L
3
)Cl]Cl, where M is Ru (8) and Os (10), and [(η6-p-cymene)MII(L
4
)Cl]Cl, where M is Ru (9) and Os (11), is reported. The compounds have been comprehensively characterized by elemental analysis, electrospray ionization mass
spectrometry, spectroscopy (IR, UV–vis, and NMR), and X-ray crystallography (L
1
·HCl, 4·H2O, 5, and 9·2.5H2O). Structure–activity relationships with regard to cytotoxicity and cell cycle effects in human cancer cells as well as cyclin-dependent
kinase (cdk) inhibition and DNA intercalation in cell-free settings have been established. The metal-free indolo[3,2-c]quinolines inhibit cancer cell growth in vitro, with IC50 values in the high nanomolar range, whereas those of the related indolo[3,2-d]benzazepines are in the low micromolar range. In cell-free experiments, these classes of compounds inhibit the activity of
cdk2/cyclin E, but the much higher cytotoxicity and stronger cell cycle effects of indoloquinolines L
1
and 7 are not paralleled by a substantially higher kinase inhibition compared with indolobenzazepines L
4
and 11, arguing for additional targets and molecular effects, such as intercalation into DNA. 相似文献
6.
The sorptive behavior of bacteria—iron oxide composites was investigated in batch metal sorption assays using ferrihydrite in isolation (0.13 and 0.14 g/L ferrihydrite in cadmium and lead systems, respectively) as well as in combination with Bacillus subtilis (0.25 g/L adsorbent mixture) and Escherichia coli (0.27 g/L adsorbent mixture). A pH range from 3.0 to 6.5 was studied using total metal concentrations of 1.0 × 10 ? 4.0 and 3.2 × 10 ? 5 M with adsorbent mixtures proportioned on a 1:1 mass/volume basis. The log of the apparent surface complex formation constants (log K S M ) and sorption capacity (S max ) values were determined by fitting the experimental data to one-site Langmuir sorption isotherms. The one-site model effectively described the sorption data (r 2 > 0.9), where Cd 2 + exhibited somewhat lower sorption affinities (log K S M = ?3 for ferrihydrite, ?1.7 for B. subtilis–ferrihydrite, and ?1.1 for E. coli–ferrihydrite) than Pb 2 + (log K S M = ?0.9 for ferrihydrite, ? 0.2 forB. subtilis–ferrihydrite, and –0.1 for E. coli–ferrihydrite). The corresponding S max values for Cd 2 + and Pb 2 + on ferrihydrite were 0.78 mmole/g and 1.34 mmole/g, respectively. For the B. subtilis–ferrihydrite composites, Cd 2 + and Pb 2 + S max values were lower at 0.29 mmole/g and 0.5 mmole/g, respectively. Similar values were determined for the E. coli–ferrihydrite composites (0.15 mmole/g and 0.68 mmole/g for Cd 2 + and Pb 2 + , respectively). The sorption of Cd 2 + and Pb 2 + by each of the sorbent systems exhibited a strong dependence on pH with sorption edges in the range of pH 4.0 to 7.3. The observed S max of the composites were lower than values predicted upon available site additivity (Cd 2 + B. subtilis ?ferrihydrite : 0.29 mmole/g (observed) < 0.57 mmole/g (calculated); Cd 2 + E. coli ?ferrihydrite : 0.15 mmole/g (observed) < 0.44 mmole/ g (calculated); Pb 2 + B. subtilis ?ferrihydrite : 0.5 mmole/g (observed) < 0.805 mmole/g (calculated); Pb 2 + E. coli –ferrihydrite : 0.68 mmole/g (observed) < 0.775 mmole/g (calculated)), implying that a masking of reactive surface sites by attachment had occurred between the bacteria and ferrihydrite. Electrophoretic mobility analysis indicated that the ferrihydrite surface properties dominate the net surface charge for each composite system with lesser contributions from the bacteria. 相似文献
7.
Mamta Tripathi Chandra Gopal Giri Devashish Das Rama Pande Sougata Sarkar Santanab Giri 《Nucleosides, nucleotides & nucleic acids》2013,32(10):563-584
AbstractAzo linked salicyldehyde and a new 2-hydroxy acetophenone based ligands (HL1 and HL2) with their copper(II) complexes [Cu(L1)2] (1) and [Cu(L2)2] (2) were synthesized and characterized by spectroscopic methods such as 1H, 13C NMR, UV–Vis spectroscopy and elemental analyses. Calculation based on Density Functional Theory (DFT), have been performed to obtain optimized structures. Binding studies of these copper (II) complexes with calf thymus DNA (ct-DNA) and torula yeast RNA (t-RNA) were analyzed by absorption spectra, emission spectra and Viscosity studies and Molecular Docking techniques. The absorption spectral study indicated that the copper(II) complexes of 1 and 2 had intrinsic binding constants with DNA or RNA in the range of 7.6?±?0.2?×?103?M?1 or 6.5?±?0.3?×?103M?1 and 5.7?±?0.4?×?104 M?1 or 1.8?±?0.5?×?103 M?1 respectively. The synthesized compounds and nucleic acids were simulated by molecular docking to explore more details mode of interaction of the complexes and their orientations in the active site of the receptor. 相似文献
8.
Barbara?Biondi Elisa?Giannini Lucia?Negri Pietro?Melchiorri Roberta?Lattanzi Federica?Rosso Luigi?Ciocca Raniero?Rocchi
Summary Syntheses are described of new endomorphin 1 and 2 peptoid–peptide hybrids in which Tyr1 and either one or both Phe3 and Phe4 have been replaced by N-substituted-glycine. The preparation is also described of two glycosylated Hyp2-endomorphin 2 analogues in which either 2,3,4,6-tetra-O-acetyl glucose or glucose are β-O-glycosidically linked to the hydroxyproline residue. The Hyp2-endomorphin sequences have also been elongate by adding a C-terminal β-alanine residue and several linear dimers have been prepared by coupling either the native peptides or the modified analogues. The cyclo endomorphin 2 has also been synthesized. Preliminary pharmacological experiments on isolated organ preparations showed that the agonist activities of both endomorphin 1 and 2 are not significantly affected by the Pro/Hyp substitution. Phe4/Nphe substitution in the endomorphin 1 reduced the potency on guinea pig ileum (GPI) by about 100 times and abolished the agonist activity on mouse vas deferens (MVD) preparation. The decrease of the agonist activity induced by modification of one phenylalanine residue only, either Phe3 or Phe4, is lower on endomorphin 2. Either modification of both Phe3 and Phe4 or glycosylation of the Hyp2-endomorphin 2 cancelled any agonist activity on both preparations. The linear peptide dimers [endomorphin 1]2, [endomorphin 2]2, [Hyp2-endomorphin 1]2, [Hyp2-endomorphin 2]2, [Hyp2-endomorphin 1-Hyp2-endomorphin 2]2 or [Hyp2-endomorphin 2-Hyp2-endomorphin 1]2, are 7–19 times less potent than endomorphin 1 on GPI and significantly less active than endomorphins 1 and 2 on MVD. The other afforded modifications significantly affected or abolished the agonist activity of the resulting endomorphin analogues on both GPI and MVD preparations.The α-amino acid residues are of the L-configuration. Standard abbreviations for amino acid derivatives and peptides are according to the suggestions of the IUPAC-IUB Commission on Biochemical Nomenclature (1984) Eur. J. Biochem., 138, 9–37. Abbreviations listed in the guide published in (2003) J. Peptide Sci., 9, 1–8 are used without explanation. 相似文献
9.
Yoshihito Ueno Shinji Ishihara Yasutomo Ito Yukio Kitade 《Nucleosides, nucleotides & nucleic acids》2013,32(4-6):475-487
The synthesis and properties of oligonucleotides (ONs) containing 9-(2,3,4-trihydroxybutyl)adenine, A C2 and A C3, are described. The ON containing A C2 involves the 3′ → 4′ and 3′ → 5′ phosphodiester linkages in the strand, whereas that containing A C3 possesses the 3′ → 4′ and 2′ → 5′ phosphodiester linkages. It was found that incorporation of the analogs, A C2 or A C3, into ONs significantly reduces the thermal and thermodynamic stabilities of the ON/DNA duplexes, but does not largely decrease the thermal and thermodynamic stabilities of the ON/RNA duplexes as compared with the case of the ON/DNA duplexes. It was revealed that the base recognition ability of A C2 is greater than that of A C3 in the ON/RNA duplexes. 相似文献
10.
Interaction of (2′ -5′) and (3′ -5′) Linked 2-Aminoadenylyl-3-aminoadenosines with Polyuridylic Acid
Masako Muraoka Seizo Takahashi Seiichi Uesugi 《Nucleosides, nucleotides & nucleic acids》2013,32(7):1503-1518
Abstract 2′-5′ and 3′-5′ linked 2-aminoadenylyl-2-aminoadenosines [(2′-5′)n2Apn2A (1) and (3′-5′)n2Apn2A (2)] were synthesized by condensation of 5′-O-monomethoxytrityl-N 2 N 6-dibenzoyl-2-aminoadenosine and N 2,N 6,2′,3′-O-tetrabenzoyl-2-aminoadenosine 5′-phosphate using dicyclohexylcarbodiimide (DCC). The conformational properties of these dimers 1 and 2 were examined by UV, NMR and CD spectroscopy. The results reveal that the 2′-5′-isomer 1 takes a stacked conformation, which contains a larger base-base overlap and is more stable against thermal perturbation with respect to the 3′-5′-isomer 2. Interactions of 1 and 2 with polyuridylic acid (Poly (U)) were also examined by Tm, mixing curves, UV and CD spectra. Both the dinucleoside isomers 1 and 2 formed a complex of 1 : 2 stoichiometry with poly(U), which was much more stable than that of the corresponding ApA isomer 相似文献
11.
Abstract The synthesis of phosphoramidites (2 and 3) derived from hypoxanthine and isoguanine N7-21-deoxyribonucleosides is described. Solid-phase synthesis furnishes oligonucleotides containing N7-glycosylated purines. New base pairs between purine N7- and N9-nucleosides are proposed. 相似文献
12.
Lilliam Casillas-Martinez Millie L. Gonzalez Zamara Fuentes-Figueroa Cyd M. Castro Deborah Nieves-Mendez Carmen Hernandez 《Geomicrobiology journal》2013,30(6):269-281
Seasonal variations in precipitation changed the community composition and microbial activity in a hypersaline, tropical microbial mat, in Cabo Rojo, PR. Using a combination of dissection, light, and transmission electron microscopy, terminal restriction fragment length polymorphism (T-RFLP), in situ microelectrode studies, and 35 S isotope incubations, we documented the major differences between wet and dry seasons. During the wet season (precipitation 177 mm), cyanobacterial (green layer) and anoxyphototrophic (pink layer) communities, as well as the black FeS layer were well-developed, and T-RFLP patterns indicated a diverse community. The rate of oxygenic photosynthesis was 49 μ M min ? 1 . Aerobic respiration was 29 μ M min ? 1 , and sulfate reduction was 264 nmol cm ? 3 h ? 1 . During the dry season (precipitation 51 mm), cyanobacteria and anoxyphototrophs were less diverse and abundant, and T-RFLP patterns were less complex. The O 2 production rate was reduced to 9 μ M min ? 1 , as was O 2 consumption (7 μ M min ? 1 ) and sulfate reduction (26 nmol cm ? 3 h ? 1 ). Aragonite, calcite, halite, and quartz were the predominant minerals. Seasonal differences were found in the green and pink layers for both halite and quartz. Gypsum was not observed, likely due to a sample handling artifact. The fluctuations in community composition and metabolic activity, principally reflected in fluctuations in binding and trapping potential of the uppermost mat community, might be responsible for the observed differences in mineralogy. 相似文献
13.
The building blocks fac-[99mTc{κ3-HB(timMe)3}(CO)3] and fac-[99mTc{κ3-R(μ-H)B(timMe)2}(CO)3] [R is H (4a), Ph (5a); timMe is 2-mercapto-1-methylimidazolyl] were obtained almost quantitatively by reacting fac-[99mTc(CO)3(H2O)3]+ with the corresponding scorpionate. These compounds cross the intact blood–brain barrier in mice, with significant retention in the case of 4a and 5a. Using 4a as the lead structure, we have synthesized the functionalized complexes fac-[M{κ3-H(μ-H)B(timBu-pip)2}(CO)3] [M is Re (8), 99mTc (8a); timBu-pip is methyl[4-((2-methoxyphenyl)-1-piperazinyl)butyl](2-mercapto-1-methylimidazol-5-yl)methanamide] and fac-[M{κ
3-H(μ-H)B(timMe)(timBu-pip)}(CO)3] [M is Re (9), 99mTc (9a)] and evaluated their potential as radioactive probes for the targeting of brain 5-HT1A serotonergic receptors. The Re complexes exhibit excellent affinity [IC50=0.172 ± 0.003 nM (8); IC50=0.65 ± 0.01 nM (9)] for the 5-HT1A receptor. The radioactive congeners (99mTc) have shown an initial brain uptake of 1.38 ± 0.46%ID g−1 (8a) and 0.43 ± 0.12%ID g−1 (9a), but suffer from a relatively fast washout. 相似文献
14.
Yu-Chi Hsieh Jiun-Ly Chir Shih-Tse Yang Shau-Jiun Chen Ching-Han Hu An-Tai Wu 《Carbohydrate research》2011,(7):10818
A sugar-aza-crown ether (SAC)-based fluorescent sensor 4 was prepared. It contains a pyrene as the fluorophore and its fluoroionophoric properties toward transition metal ions were investigated. Chemosensor 4 exhibits highly selective recognition toward Cu2+ and Hg2+ ions among a series of tested metal ions in methanol solution. The association constants for 4*Cu2+ and 4*Hg2+ in methanol solution were calculated to be 7.4 × 101 M−1 and 4.4 × 103 M−1, respectively. Chemosensor 4 formed complexes with the Cu2+ or Hg2+ ion at a 1:1 ligand-to-metal ratio with a detection limit of 1.3 × 10−4 M Cu2+ and 1.26 × 10−5 M Hg2+, respectively. 相似文献
15.
《Nucleosides, nucleotides & nucleic acids》2013,32(5-8):865-868
Abstract Two dinucleoside polyphosphate NAD analogs, P1-(adenosine-5′)-P3-(nicotinamide riboside-5′)triphosphate (Np3A, 1) and P1-(adenosine-5′)-P4-(nicotinamide riboside-5′)tetraphosphate (Np4A, 2), were synthesized and tested as inhibitors of both microbial and human recombinant NMN adenylyltransferase. Compounds 1 and 2 proved to be selective inhibitors of microbial enzymes. 相似文献
16.
Saied Ghadimi Ali Asghar Ebrahimi Valmoozi Mehrdad Pourayoubi Keyvan Asad Samani 《Journal of enzyme inhibition and medicinal chemistry》2013,28(4):556-561
Phosphoramido acid esters (CH3)2NP(O)X(p-OC6H4-CH3) (containing P-Cl (1), P-O (2), P-F (3), P-CN (5), and P-N (4,6) bonds, X for 2, 4 and 6 is OCH3, (C2H5)2N and morpholin) have been synthesized to investigate the structure-activity study of AChE enzyme inhibition, through the parameters logP, δ31P and IC50. After their characterization by 31P, 31P{1H}, 13C, 1H NMR, IR and mass spectroscopy, the parameters logP and δ31P (31P chemical shift in NMR) were used to evaluated the lipophilicity and electronical properties. The ability of compounds to inhibit human AChE was predicted by PASS software (version 1.193), and experimentally evaluated by a modified Ellman's assay. 相似文献
17.
Wajdi Michel Zoghaib Shajan Mannala V. Sagar Gupta Guy Tourigny 《Nucleosides, nucleotides & nucleic acids》2013,32(4):364-376
Analogs of (E)-5-(2-bromovinyl)-2 ′-deoxycytidine (BrVdCyd) (1) by substitution at N4 were synthesized to impart resistance against deamination. The anti-HSV-1 activity and solution conformation of these analogs were determined. N4-Acetyl-BrVdCyd (2) was a potent inhibitor of HSV-1 replication whereas N4-propanoyl-BrVdCyd (3) had good activity and N4-Butanoyl-BrVdCyd (4) had only low activity against HSV-1 replication. N4-Methyl-BrVdCyd (5) was devoid of activity against HSV-1. 相似文献
18.
Joseph B. Yavitt Nathan Basiliko Merritt R. Turetsky Anthony G. Hay 《Geomicrobiology journal》2013,30(8):641-651
Because recent patterns of permafrost collapse in boreal peatlands appear to enhance emissions of CH 4 to the atmosphere, we examined methanogenesis and methanogen diversity in peat soil from peatlands with and without permafrost in two peatland complexes situated in continental western Canada. Peat soil from the active layer of permafrost bogs had very low rates of CH 4 production (ca. 10 nmol g ?1 day ?1 ), and we were unable to PCR-amplify 16s rRNA gene sequences using Archaea-specific primers in four peat samples. Surface peat soil from continental bogs with no permafrost supported moderate rates of CH 4 production (20–600 nmol g ?1 day ?1 ), with maximum rates in soil located close to the mean water table level. Additions of ethanol stimulated CH 4 production rates, suggesting metabolic substrate limitations. Peat from internal lawns, which have experienced surface permafrost degradation in the past 150 years, had very rapid rates of CH4 production (up to 800 nmol g ?1 day ?1 ) occurring within the soil profile. Concomitant rates of anaerobic CO 2 production were greater in continental bogs (ca. 6 μmol g ?1 day ?1 ) than in internal lawns (ca. 4 μ mol g ?1 day ?1 ) or in permafrost bogs (2.8 μ mol g ?1 day ?1 ). Analysis of the 16s rRNA gene for Archaea in the continental bog indicated mostly sequences associate with Methanobacteriales and RC-I with a Methanosarcinaceae sequence in the deepest peat soil. In the internal lawn, Methanosarcinaceae were most common in peat soil with a Methanosaetaceae sequence in the deepest peat soil. This study showed that patterns of discontinuous permafrost and ongoing permafrost degradation in boreal regions create patchy soil environments for methanogens and rates of methanogenesis. 相似文献
19.
《Nucleosides, nucleotides & nucleic acids》2013,32(1-2):59-75
The nucleophilic addition–elimination reaction of 2′,3′,5′-tri-O-acetyl-2-fluoro-O 6-[2-(4-nitrophenyl)ethyl]inosine (8) with [15N]benzylamine in the presence of triethylamine afforded the N 2-benzyl[2-15N]guanosine derivative (13) in a high yield, which was further converted into the N 2-benzoyl[2-15N] guanosine derivative by treatment with ruthenium trichloride and tetrabutyl-ammonium periodate. A similar sequence of reactions of 2′,3′,5′-tri-O-acetyl-2-fluoro-O 6-[2-(methylthio)ethyl]inosine (9) and the 6-chloro-2-fluoro-9-(β-D-ribofuranosyl)-9H-purine derivative (11), which were respectively prepared from guanosine, with potassium [15N]phthalimide afforded the N 2-phthaloyl [2-15N]guanosine derivative (15; 62%) and 9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-6-chloro-2-[15N]phthalimido-9H-purine (17; 64%), respectively. Compounds 15 and 17 were then efficiently converted into 2′,3′,5′-tri-O-acetyl[2-15N]guanosine. The corresponding 2′-deoxy derivatives (16 and 18) were also synthesized through similar procedures. 相似文献
20.
E. Sochacka 《Nucleosides, nucleotides & nucleic acids》2013,32(1-3):327-338
Abstract E. coli tRNALys anticodon loop fragment (Umnm5sUUUt6A) 1 and its analogues 2–6 were synthesized by the classical phosphotriester approach in solution. The preparation of suitably protected derivatives of N6-threonylcarbamoyladenosine 18 is also described. 相似文献