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1 1 on both alpha-KG and glutarate (another C5-dicarboxylate).
2 Me2NH2)[In(ABDC)2] (ABDC, 2-aminobenzene-1,4-dicarboxylate).
3 MOF-74, DOBDC(4-) = 2,5-dihydroxybenzene-1,4-dicarboxylate).
4 dehyde and methyl carbon atoms to form a 1,2-dicarboxylate.
5 hyl spiro[cycloprop[2]ene-1,9'-fluorene]-2,3-dicarboxylate.
6 te reuptake blocker, l-trans-pyrrolidine-2,4-dicarboxylate.
7 obtained in one case with dimethyl acetylene dicarboxylate.
8  nitrogen, and 4 carboxylate of pyridine 2,4-dicarboxylate.
9 ate, but not by succinate, a nonexchangeable dicarboxylate.
10 ng buffer containing one fully (13)C-labeled dicarboxylate.
11  PA5530 gene was induced by extracellular C5-dicarboxylates.
12 onies and grew poorly on organic nitrogen or dicarboxylates.
13 ns and substrate specificity for four-carbon dicarboxylates.
14 ated that retained some ability to transport dicarboxylates.
15 2 mediate Na(+)-coupled transport of various dicarboxylates.
16 cells that shows preference for citrate over dicarboxylates.
17 a novel asymmetric alkylation of allylic gem-dicarboxylates.
18 ,5S,6R-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate) (0.3, 1.0, and 3.0 mg/kg, s.c.) dose depe
19 agonist APDC [(2R,4R)-4-aminopyrrolidine-2,4-dicarboxylate] (0.1 mum) or group III agonist l-(+)-2-am
20 1S,2S,5R,6S)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate 1 (LY354740) bearing C4-thiotriazole subst
21 cycloaddition of dimethyl cyclobut-1-ene-1,2-dicarboxylate (1) with cyclohexene (7) afforded two phot
22  4-methyl (1R,2S,4R)-2-methylcyclohexane-1,4-dicarboxylate (+)-1, via palladium-catalyzed methoxycarb
23  these compounds are maleate (7), allene-1,3-dicarboxylate (10), cis,cis-muconate (11), trans,trans-m
24 e (4Z,10Z)-dimethyl cyclodeca-4,10-diene-1,4-dicarboxylate (10), which subsequently isomerized to pro
25 pyridine (10), dimethyl 2,2'-bipyridine-4,4'-dicarboxylate (11), 1,10-phenanthroline (12), 2,9-dimeth
26          In a previous report, we discovered dicarboxylate 1a (PF-06649298) which inhibits the transp
27 ,6S-2-amino-4-methylbicyclo[3.1.0]hexane-2,6-dicarboxylate 2 (LY541850), exhibited an unexpected mGlu
28  is about 2000, releasing cyclopentanone-2,4-dicarboxylate (22) and two other precursors of this comp
29 oxylated 2E-fluoro-2,4-pentadienoate and the dicarboxylated 2E-fluoro-2-en-4-ynoate being the most po
30  syntheses of dimethyl 2,2'-bithiophene-4,4'-dicarboxylate (3), dimethyl 2,2'-bithiophene-3,4'-dicarb
31 eptor agonist (2R,4R)-4-aminopyrrolidine-2,4-dicarboxylate (3.0 microg/side) mimicked the effect of L
32  of a porous MOF, Zn(4)O(trans-4,4'-stilbene dicarboxylate)(3), with Br(2) results in diastereoselect
33 boxylate (3), dimethyl 2,2'-bithiophene-3,4'-dicarboxylate (4), and dimethyl 2,2'-bithiophene-3,3'-di
34 late (4), and dimethyl 2,2'-bithiophene-3,3'-dicarboxylate (5) are described.
35 ethylspiro[bicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate-7,1'-cycloprop ane] (B'), A:B', and A':B;
36 diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate (8), and i-Pr2NEt and their coupling in di
37  linkers (oxalate, 6; fumarate, 8; acetylene dicarboxylate, 9; cis,cis-muconate, 11; trans,trans-muco
38 ors (X-(CH(2))(n)-X) such as alkyl dithiols, dicarboxylate acids, and alkanethiol shells capped on na
39 odeling support a model where QFR twists the dicarboxylate, activating it for catalysis.
40        In addition, p-aminohippurate and the dicarboxylates adipate and glutarate (but not succinate
41                 With SnCl4, the cyclopropane dicarboxylates afforded cyclopentene derivatives through
42  binding to site IIf The decrease in matrix [dicarboxylate] allows O2 access to reduced site IIf, the
43 njugate was reduced by the OAT1-exchangeable dicarboxylates alpha-ketoglutarate, glutarate, and adipa
44 cribing the transport and assimilation of C5-dicarboxylates among bacteria.
45 of catalysis in the presence of 2,4-pyridine dicarboxylate, an analogue of alpha-ketoglutarate.
46 old, and concomitantly decrease the K(i) for dicarboxylate analogues of l-aspartate by up to 40-fold.
47  in conjunction with di-tert-butyl hydrazine dicarboxylate and an inorganic base provides a variety o
48 ew MOF [Yb2(BDC)3(DMF)2]H2O (BDC=benzene-1,4-dicarboxylate and DMF=N,N-dimethylformamide) under solvo
49  likely orients amino acid residues near the dicarboxylate and FAD binding site, which facilitates fo
50 col utilizes a combination of an iodobenzene dicarboxylate and iodine to functionalize a series of ac
51 de at 0.6 V, whereas diethyl 2,5-dioxahexane dicarboxylate and lithium propionate form on the Sn elec
52 + 2] cycloaddition between vinylcyclopropane dicarboxylates and 3-nitroindoles has been developed.
53 inity, disulfonic stilbene-sensitive flux of dicarboxylates and citrate across the plasma membrane by
54  3a) are capable of regioselectively binding dicarboxylates and pyrophosphate (H(2)PPi(2-)).
55 DH4) contain all key residues for binding of dicarboxylates and quinones, but the enzyme showed the l
56                                              Dicarboxylates and sucrose are the main carbon sources w
57     The transporter does interact with other dicarboxylates and tricarboxylates but with considerably
58 , Co, Ni; dobdc(4-) = 2,5-dioxidobenzene-1,4-dicarboxylate) and M(2)(m-dobdc) (m-dobdc(4-) = 4,6-diox
59 7 ([Zr6O4(OH)4 (bpdc)6], bpdc: 4,4'-biphenyl dicarboxylate) and UiO-abdc ([Zr6O4(OH)4 (abdc)6], abdc:
60 y structures of MOFs UWDM-2 (1,4-diazophenyl-dicarboxylate) and UWDM-3 (1,4-biphenyl-dicarboxylate) s
61 ghest reported affinity to date for these C4-dicarboxylates, and to succinate (K(d) = 110 nM) and fum
62 not group II [(2R,4R)-4-aminopyrrolidine-2,3-dicarboxylate] and III [L-AP 4 (L-(+)-2-amino-4-phosphon
63 on of stereo- and E/Z geometric isomers of a dicarboxylate anion guest is described.
64 ne (PC), and sphingomyelin (SM) cations with dicarboxylate anions are shown to charge-invert the posi
65  studied as receptors for the recognition of dicarboxylate anions of varying chain length in aqueous
66 ape complementarity between the host and the dicarboxylate anions, which is nicely reflected in the s
67 ared to play a major role in the presence of dicarboxylate anions.
68 h respect to its ability to bind alpha,omega-dicarboxylate anions.
69 ajectory of S. Typhimurium implicates the C4-dicarboxylate antiporter DcuABC in early murine gut colo
70 mGluR agonists (2R,4R-4-aminopyrrolidine-2,4-dicarboxylate (APDC) and L(+)-2-amino-4-phosphonobutyric
71 3)) agonists (2R, 4R)-4-aminopyrrolidine-2,4-dicarboxylate (APDC) or (2S,2'R,3'R)-2-(2'3'-dicarboxycy
72  mGluR agonist, 2R,4R 4-aminopyrrolidine-2,4-dicarboxylate (APDC), did not alter thermal sensitivity
73 es of a cooperative pinwheel chemosensor for dicarboxylates are described.
74                           To explore whether dicarboxylates are important for growth of DC3000 in the
75 indicating that transport and utilization of dicarboxylates are important for virulence of DC3000.
76 owly in culture than wild-type bacteria when dicarboxylates are the only available carbon source.
77                    High amounts of aliphatic dicarboxylates are usually considered as an indicator of
78 ) and dimethyl 3,5-dimethyl-1-pyrazoline-3,5-dicarboxylate as a specific organocatalyst has been foun
79 new hosts against a series of alkyl and aryl dicarboxylates as well as a range of phosphoanionic spec
80  which imports inside the cell 4 to 6 carbon dicarboxylates as well as N-acetylaspartate (NAA).
81 says, DcuABC and enzymes that convert the C4-dicarboxylates aspartate and malate into fumarate (AspA,
82 other transcriptional regulators involved in dicarboxylate assimilation, suggesting that MifR might i
83                     Synthesis of a ruthenium dicarboxylate at a low temperature allowed for direct ob
84  transporters of dipeptides and tripeptides, dicarboxylates, auxin, and abscisic acid.
85  complex of a 1,10-phenanthroline containing dicarboxylate axle with a 1,10-phenanthroline containing
86 benzo[24]crown-8 wheels, (3) 2,6-naphthalene dicarboxylate axles with tetra-imidazolium macrocycle wh
87 ary for transport was a four-carbon terminal dicarboxylate backbone and that productive substrate-tra
88 phiphilic ligand, 4'-tert-butyl-biphenyl-3,5-dicarboxylate (BBPDC), with Zn(NO(3))(2), Co(NO(3))(2),
89 O) as axial ligands and 2,2'-bipyridine-6,6'-dicarboxylate (bda) as the equatorial ligand, we have sy
90 of nonpolar functional groups on the benzene dicarboxylate (BDC) linker in the pillared DMOF-1 [Zn2(B
91  to the conservation of amino acids near the dicarboxylate binding sites of the two enzymes is that t
92 have remarkable structural homology at their dicarboxylate binding sites.
93 odanine acetic acid) and DHP (PDC = pyridine dicarboxylate) binding sites.
94 ults in succinate-dependent reduction of the dicarboxylate-binding site of complex II (site IIf); (b)
95 nedicarboxylate (NDC), and BTE/biphenyl-4,4'-dicarboxylate (BPDC), to give four metal-organic framewo
96 mu-O)(3)Mn(IV)(tmtacn)](2+) into the active, dicarboxylate-bridged [(tmtacn)Mn(III)(mu-O)(mu-RCOO)(2)
97 esized using a salicylaldimine (sal)-derived dicarboxylate bridging ligand.
98 eptor unit 1 with several linear and angular dicarboxylate bridging ligands afforded hitherto unknown
99 highly stable MOFs (1 and 2) using elongated dicarboxylate bridging ligands derived from Cp*Ir(L)Cl c
100 y building units (SBUs) and anthracene-based dicarboxylate bridging ligands.
101 ed using a post-assembly modification to the dicarboxylate building block, suggesting another strateg
102   As such, a small initial difference in the dicarboxylate building blocks is amplified into distinct
103  is apparent for several of the alkylaminium dicarboxylates but not for the alkylaminium monocarboxyl
104 tion of the transport and metabolism of C(4)-dicarboxylates, but they are not highly related by seque
105 ethyl]-amino]propyl]-1,3-benzodiox azole-2,2-dicarboxylate], but not after administration of beta1, b
106  Nitrogen-fixing rhizobial bacteroids import dicarboxylates by using the DctA transporter.
107 ([Zr6O4(OH)4 (abdc)6], abdc: 4,4'-azobenzene dicarboxylate) by single-crystal nanoindentation, high-p
108 ous DEAD reagent bis(perfluorohexylethyl)azo dicarboxylate (C(6)F(13)(CH(2))(2)O(2)CN=NCO(2)(CH(2))(2
109 byproducts from bis(perfluorohexylpropyl)azo dicarboxylate (C(6)F(13)(CH(2))(3)O(2)CN=NCO(2)(CH(2))(3
110  reagent perfluorooctylpropyl tert-butyl azo dicarboxylate (C(8)F(17)(CH(2))(3)O(2)CN=NCO2(t)Bu, F-DE
111 rapid efflux of succinate/fumarate and other dicarboxylates capable of competitively binding to site
112           We revealed that genipin activated dicarboxylate carrier and decreased the activity of UCP1
113 pt abundance of genes encoding mitochondrial dicarboxylate carrier proteins.
114  such as overexpression of the mitochondrial dicarboxylate carrier result in increased ROS formation
115                                      The Na+/dicarboxylate co-transporter, NaDC-1, from the kidney an
116                                          The dicarboxylate competitive inhibitor, (2E)-fluoromuconate
117 ecedented selectivity for fum(2-) over other dicarboxylate competitors, including its cis isomer male
118                                  Rhodium(II) dicarboxylate complexes were discovered to catalyze the
119 ues, Arg-349 and Asp-373, of the renal Na(+)/dicarboxylate cotransporter (NaDC-1) have been shown in
120                                      The Na+/dicarboxylate cotransporter (NaDC1) is involved in the a
121                                      The Na+/dicarboxylate cotransporter 1 (NaDC1) is a low-affinity
122   SLC13A3 encodes the plasma membrane Na(+) /dicarboxylate cotransporter 3, which imports inside the
123                                    The Na(+)/dicarboxylate cotransporter NaDC1 absorbs citric acid cy
124                              The human Na(+)/dicarboxylate cotransporter NaDC3 (SLC13A3) is found in
125                                    The Na(+)/dicarboxylate cotransporter transports Na(+) with citric
126 ithin the substrate access pore of the Na(+)/dicarboxylate cotransporter, either in a transmembrane h
127 uctural similarity to the members of the Na+-dicarboxylate cotransporter/Na+ -sulfate cotransporter (
128                                    The Na(+)/dicarboxylate cotransporters (NaDC1) from mouse (m) and
129 aureus is a homologue of the mammalian Na(+)/dicarboxylate cotransporters (NaDC1) from the solute car
130 t sequence homology with the mammalian Na(+)/dicarboxylate cotransporters NaDC-1 and NaDC-3.
131 ily, a group that includes the mammalian Na+/dicarboxylate cotransporters NaDC1 and NaDC3.
132  the SLC13 family that also includes the Na+/dicarboxylate cotransporters, NaDC.
133 that also includes the mammalian SLC13 Na(+)/dicarboxylate cotransporters, NaDC1 and NaCT.
134 elopment of specific inhibitors of the Na(+)/dicarboxylate cotransporters.
135 [M8L12] (M=In/Cr, L=dinegative 4,5-imidazole-dicarboxylate) cubane-like structure.
136 arboxylation of nine zwitterionic pyridinium dicarboxylates (D(x,y)) are reported.
137 pane rings in 2'-aryl-1,1'-bicyclopropyl-2,2-dicarboxylates (D-A bicyclopropyl, ABCDs) in the presenc
138  units and a mixture of 2,2'-bipyridine-5,5'-dicarboxylate (dcbpy) and 1,4-benzenediacrylate (pdac) l
139 hoxy-5,6,5',6'-dimethylenedioxybiphenyl-2,2'-dicarboxylate (DDB) analogues were designed and synthesi
140  gene encodes 3-hydroxy-2-methylpyridine-4,5-dicarboxylate decarboxylase (HMPDdc), an enzyme involved
141 nsporter function by L-trans-pyrrolidine 2,4-dicarboxylate decreased the rate of glutamate uptake but
142 8 [(-)-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate] decreased nicotine, but not food, self-ad
143 carboxylates and 1.1 to 2.2 for alkylaminium dicarboxylates, dependent on the molecular functionality
144 -anisylformamidinate), linked by unsaturated dicarboxylate dianions of various lengths have been prep
145 conium nitrogen bond, forming a C2 symmetric dicarboxylated diazenido compound.
146                                 However, the dicarboxylate (DIC) and 2-oxoglutarate (OGC) carriers lo
147                             We also identify dicarboxylate dimers as a novel proton sensor in protein
148  phthalates and di(isononyl) cyclohexane-1,2-dicarboxylate (DINCH) in 656 urine samples collected fro
149 ith a 90 degrees Pt(II) acceptor and various dicarboxylate donors in a 1:1:2 ratio.
150 rate levels, we hypothesize that by allowing dicarboxylate efflux from the matrix, PTP opening during
151  PA5530 gene in response to extracellular C5-dicarboxylates, especially alpha-KG.
152              Strikingly lower lysolipids and dicarboxylated fatty acids were seen in obese children.
153 ydrogenation of dibenzyl 5-dipyrroketone-2,9-dicarboxylates followed by decarboxylative iodination af
154 ann reaction of 2-naphthols with acetone-1,3-dicarboxylates, followed by an intramolecular Friedel-Cr
155 legans may lead to decreased availability of dicarboxylates for cellular production of metabolic ener
156 feature a new preparation of cis-cyclobutane dicarboxylates from commercially available coumalate sta
157  Thus, SdcS facilitates the transport of the dicarboxylates fumarate, malate, and succinate across th
158                                     The C(4)-dicarboxylate (fumarate) responsive sensor kinase DcuS o
159 BDC) (H2DHBDC(2-) = 2,5-dihydroxybenzene-1,4-dicarboxylate) function as selective sensors for ammonia
160 selectivity follows: phenolates >/= aromatic dicarboxylates > aromatic monocarboxylates > benzenesulf
161 where TTh-CO2 = 2,2':5',2''-terthienyl-5,5''-dicarboxylate, has also been prepared and employed in th
162       The presence of substantial amounts of dicarboxylates in cuticular membranes is unexpected.
163 des olefins along with unsaturated mono- and dicarboxylates in distributions with adjustable widths.
164 ntributes to favorable binding constants for dicarboxylates in water, as well as a high degree of sel
165 ,5S,6R-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate) in adult, but not prepubertal, mice born
166 oncentrations of cerebrospinal fluid NAA and dicarboxylates (including alphaKG) were observed.
167 da(2-) being [2,2':6',2''-terpyridine]-6,6''-dicarboxylate, including complex [Ru(IV)(OH)(tda-kappa-N
168 agonist APDC [(2R,4R)-4-aminopyrrolidine-2,4-dicarboxylate] induced a concentration-dependent decreas
169   In Staphylococcus aureus, the transport of dicarboxylates is mediated in part by the Na+-linked car
170 iethylbenzene head unit, the affinity toward dicarboxylates is significantly reduced.
171 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate) is characterized for the removal of CO2 f
172 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate), is shown to undergo a topotactic oxidati
173 I)(bda)(isoq)2] (bda is 2,2'-bipyridine-6,6'-dicarboxylate; isoq is isoquinoline) exists as the open-
174 with Na(+) (K(0.5) of 2.7 mM) binding before dicarboxylate (K(m) of 4.5 microM).
175 side the square openings of neighboring zinc dicarboxylate layers.
176  molecular clip 6 and three different linear dicarboxylates led to the formation of neutral molecular
177                                          The dicarboxylate ligand in oxaloacetate-containing crystals
178 -bipyridine, ppy = 2-phenylpyridine) derived dicarboxylate ligands (DBB-Ir) and then loaded with Well
179 d 2) built from [Ir(ppy)(2)(bpy)](+)-derived dicarboxylate ligands (L(1) and L(2)) and Zr(6)(mu(3)-O)
180  than those of the analogous polyunsaturated dicarboxylate linked compounds and reveal at least two s
181 lt with a high-symmetry bicyclo[2.2.2]octane dicarboxylate linker in a Zn4O cubic lattice.
182 nic framework (MOF) based on a BINAP-derived dicarboxylate linker, BINAP-MOF, was synthesized and pos
183 nstructed from only bipyridyl-functionalized dicarboxylate linker, both mBPV- and mPT-MOF were built
184 th four methyl groups decorating the benzene dicarboxylate linker, leads to a smooth transition from
185 , the colors upon the chemical nature of the dicarboxylate linker.
186  demonstrated using the 2,2'-bipyridine-5,5'-dicarboxylate linker; it is energetically prohibitive fo
187  chemically unsaturated and fully conjugated dicarboxylate linkers (oxalate, 6; fumarate, 8; acetylen
188 /H2O ligands, subsequent insertion of linear dicarboxylate linkers is achieved.
189  alone, implying that the pi system of these dicarboxylate linkers is mediating communication.
190 tu ligand exchange with progressively longer dicarboxylate linkers is performed on single crystalline
191 3+), Yb(3+)) and linear amino-functionalized dicarboxylate linkers of different lengths.
192 I), were prepared using purely BINAP-derived dicarboxylate linkers or by mixing BINAP-derived linkers
193  BINAP-derived linkers with unfunctionalized dicarboxylate linkers, respectively.
194                         As identified by the dicarboxylate linkers, these compounds are maleate (7),
195 rved with those compounds having unsaturated dicarboxylate linkers.
196 nanthryl-functionalized and unfunctionalized dicarboxylate linkers.
197  1S,2S,5R,6S-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate (LY354740), a potent and pharmacologically
198  (-)-4-Amino-2-thiabicyclo-[3.1.0]hexane-4,6-dicarboxylate (LY389795, (-)-3) is a highly potent and s
199                   In contrast, the saturated dicarboxylates maintained a constant level during seed d
200 te citramalyl-CoA, an intermediate in the C5-dicarboxylate metabolic pathway that includes itaconate,
201 in the methane, pyruvate, and glyoxylate and dicarboxylate metabolic pathways.
202 linoleic acid metabolism, and glyoxylate and dicarboxylate metabolism were mainly enriched.
203 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate; mmen = N,N'-dimethylethylenediamine) was
204 ive Ru-bda type (bda is 2,2'-bipyridine-6,6'-dicarboxylate) molecular OER catalysts are proposed to o
205 sotope shifts implies that a wide variety of dicarboxylate monanions are asymmetric, present as a rap
206 (13)C NMR chemical shifts of cyclohexene-1,2-dicarboxylate monoanion in chloroform-d and on the (19)F
207 he hydrogen bond in hydrogen cyclohexene-1,2-dicarboxylate monoanion was determined in chloroform usi
208 ers have been described to participate in C4-dicarboxylate movement across biological membranes, but
209 thynyl-6-phenyl-1,4(+/-)dihydropyridine-3 ,5-dicarboxylate (MRS1191), by the phospholipase C inhibito
210 (+)]tpy-PhCOO(-)), and disodium pyridine-2,6-dicarboxylate (Na(2)pydic).
211 l2]2, tpyCOONa, and then sodium pyridine-2,6-dicarboxylate [Na(dipic)].
212 cognition elements to cooperatively bind two dicarboxylates of varying size.
213 (4-vinylpyridine)2 (bda=2,2'-bipyridine-6,6'-dicarboxylate) on planar electrodes results in films con
214                             Oxanorbornadiene dicarboxylate (OND) reagents are potent Michael acceptor
215 ixtures (> or = 81% product) of the reactive dicarboxylate or monocarboxylate intermediates, 2 or 2-h
216 ly, the GT inhibitor l-trans-pyrrolidine-2-4-dicarboxylate (PDC) potentiated, whereas the positive GT
217 es the reversible hydrolysis of 2-pyrone-4,6-dicarboxylate (PDC) to 4-oxalomesaconate and 4-carboxy-2
218  with 100-500 microM L-trans-pyrrolidine-2,4-dicarboxylate (PDC), an inhibitor of glutamate re-uptake
219                 FsrA also represses the DctP dicarboxylate permease and the iron-sulfur-containing en
220 trate (methyl propiolate, dimethyl acetylene dicarboxylate, phenyl acetylene, ethyl 2,3-butadienoate)
221 t energy absorptions are Mo(2)(4+) delta --> dicarboxylate pi metal-to-ligand charge transfer transit
222                                           C4-dicarboxylates play a central role in cellular physiolog
223 ponent system in response to fumarate or its dicarboxylate precursors.
224 neogenesis using deaminated amino acids with dicarboxylate products of peroxisomal lipid beta-oxidati
225 xanthenone fluorescent scaffold coupled to a dicarboxylate pseudocrown ether receptor to achieve sele
226 neutral symport reaction having a 2:1 cation/dicarboxylate ratio.
227 nd radicals generated from phenyliodine(III) dicarboxylate reagents and exhibits excellent functional
228 tamate analogue PDC (L-trans-pyrrolidine-2,4-dicarboxylate), reduced the current by approximately 88%
229 n, Co, Ni and Zn; L = 2,5-dioxidobenzene-1,4-dicarboxylate) referred to as MOF-74 and CPO-27.
230  fumarate; and the dcuSR operon encoding the dicarboxylate-responsive regulatory system.
231    Saponification gave 21,23-dithiaporphyrin dicarboxylate salts 16 and 17.
232                                       The C4-dicarboxylate sensor kinase DcuS is membrane integral be
233 enyl-dicarboxylate) and UWDM-3 (1,4-biphenyl-dicarboxylate) show that both frameworks are large enoug
234 nsa-zirconocene diiodide along with the N,N'-dicarboxylated silylated hydrazine.
235 ed in substrate binding and catalysis at the dicarboxylate site.
236 trogen fixation, although they can transport dicarboxylates, some at relatively high levels.
237 ane axle component facilitates the complexed dicarboxylate species to be sensed via a fluorescence re
238 d tetraphenylethylene and one of two benzene dicarboxylate species.
239 including the SdhE assembly factor and bound dicarboxylates, stimulate covalent flavinylation by preo
240 e branched chain side chain, less so for the dicarboxylate substrate side chain.
241 ion of the protonated macrobicycles with the dicarboxylate substrates.
242 enerated a strain unable to grow on the C(4)-dicarboxylates succinate, malate, and fumarate.
243 I) lyotropic gyroid phase formed by a gemini dicarboxylate surfactant self-assembly using a combinati
244                                    The Na(+)/dicarboxylate symporter (SdcS) from Staphylococcus aureu
245                                    The Na(+)/dicarboxylate symporter from Staphylococcus aureus, name
246 ion of self-assembly in the Fe-biphenyl-4,4'-dicarboxylate system, demonstrating that coordination mo
247       A series of new zinc(II)-thiophene-2,5-dicarboxylate (tdc) MOFs based on novel dodecanuclear wh
248 portantly, we also identify a small molecule dicarboxylate that acts as an essential cofactor in this
249 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate) that feature step-shaped CO2 adsorption i
250 udied using a structurally similar series of dicarboxylated thiacyanine dyes that bind to the oxide s
251 on strategy, the [3]rotaxane host recognises dicarboxylates through the formation of 1:1 stoichiometr
252 boxylation of 3-hydroxy-2-methylpyridine-4,5-dicarboxylate to 3-hydroxy-2-methylpyridine-5-carboxylat
253 contribution of the polyolefinic alpha,omega-dicarboxylate to the molecular orbital undergoing oxidat
254 4'-(4-benzoate)-(2,2',2''-terpyridine)-5,5''-dicarboxylate (TPY) before being coordinated with iron c
255                                  A plastidic dicarboxylate translocator 1-[2-OG/malate translocator (
256 mbrane transporters, proteins involved in C4-dicarboxylate transport and utilization, enzymes for bio
257      Our results reveal a new function in C4-dicarboxylate transport by members of the poorly charact
258 n and biochemical properties of bacterial C4-dicarboxylate transport systems.
259 xylate transport family to be involved in C4-dicarboxylate transport.
260 d transporters from the tellurite-resistance/dicarboxylate transporter (TDT) family or the Na(+) coup
261     The absence of the Arabidopsis tonoplast Dicarboxylate Transporter (tDT) in the tdt knockout muta
262 3000 in the apoplast, we disrupted the dctA1 dicarboxylate transporter gene.
263 ion that increased expression of the dctA C4-dicarboxylate transporter greatly enhanced the Cit(+) ph
264  cell motility 2), SLC13A3 (sodium-dependent dicarboxylate transporter member 3), and PREX1 (phosphat
265  function of the high affinity Na(+)-coupled dicarboxylate transporter NaDC2 in C. elegans may lead t
266                             Although the NAA dicarboxylate transporter NaDC3 is primarily thought to
267 ctural modeling using the x-ray structure of dicarboxylate transporter VcINDY as template and confirm
268 a crystal structure of Vibrio cholerae Na(+)-dicarboxylate transporter VcINDY, from which we generate
269 and Pi based on the crystal structure of the dicarboxylate transporter VcINDY.
270 d functionally characterized a Na(+)-coupled dicarboxylate transporter, SdcS, from Staphylococcus aur
271         The PA5530 gene, encoding a putative dicarboxylate transporter, was found to be essential for
272 ion of the dctA gene, which encodes the C(4)-dicarboxylate transporter, was reduced in a gyrA751 muta
273 T-PCR; the three known Na+-dependent citrate/dicarboxylate transporters could not be detected.
274                                  Other Na(+)/dicarboxylate transporters from the SLC13 family, includ
275 hila melanogaster and with the Na(+)-coupled dicarboxylate transporters NaDC1 and NaDC3 identified in
276 the differential substrate specificity among dicarboxylate transporters that underpin their diverse b
277 functionally characterized two Na(+)-coupled dicarboxylate transporters, namely ceNaDC1 and ceNaDC2,
278 cassette superfamily and telurite-resistance/dicarboxylate transporters.
279 on/Na(+) symporter (DASS) family translocate dicarboxylate, tricarboxylate or sulphate across cell me
280 ceptor cyclopropanes (2-arylcyclopropane-1,1-dicarboxylates) under double-catalysis conditions by tre
281 iral monomeric all-cis 5-arylpyrrolidine-2,4-dicarboxylate units were synthesized for the first time
282        trans-2-Aryl-3-nitro-cyclopropane-1,1-dicarboxylates, upon treatment with BF3.OEt2, undergo ri
283 as prepared from diethyl 2-nitropyrrole-3,4,-dicarboxylate via an alkylation, ammonolysis, reduction
284 on of trans-2-aroyl-3-styrylcyclopropane-1,1-dicarboxylates was investigated with different Lewis aci
285 m catalyzed dimerization of oxanorbornadiene dicarboxylates was studied.
286 imple inorganic ions, halides, and mono- and dicarboxylates was taken into account.
287  hydroxamates derived from trans-cyclopropyl dicarboxylate were examined as potential TNF-alpha conve
288 he alkylation of di-tert-butyl hydrazine-1,2-dicarboxylate were investigated.
289                A wide variety of oxetane 2,2-dicarboxylates were accessed in high yields, including f
290                                        These dicarboxylates were found predominantly in epidermal pee
291 f 4-oxo-2,4-dihydrocyclopenta[c]chromene-1,2-dicarboxylates were obtained in moderate to good yields
292                       The m- and p-carborane dicarboxylates were utilized as the donor linkers in con
293 dobdc) (m-dobdc(4-) = 4,6-dioxidobenzene-1,3-dicarboxylate), which all contain a high density of coor
294 ork, we trans-hydrogenate [1-(13)C]acetylene dicarboxylate with para-enriched hydrogen using a commer
295 nding is observed for dicarboxylic acids and dicarboxylates with four-carbon chains, and the binding
296         The ring-opening of cyclopropane-1,1-dicarboxylates with vicinal donor aryl groups by boronic
297 s, Ru(bda)(L)(2) (bda = 2,2'-bipyridine-6,6'-dicarboxylate) with phosphonate or pyridyl sites for wat
298 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate) with the cyclic diamine 2-(aminomethyl)pi
299 ceptors form more endothermic complexes with dicarboxylates, with a favorable entropy of association.
300 electron spectra of nine isomeric pyridinium dicarboxylate zwitterions and three nonzwitterionic meth

 
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