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1 Me2NH2)[In(ABDC)2] (ABDC, 2-aminobenzene-1,4-dicarboxylate).
2 MOF-74, DOBDC(4-) = 2,5-dihydroxybenzene-1,4-dicarboxylate).
3 1 on both alpha-KG and glutarate (another C5-dicarboxylate).
4 te reuptake blocker, l-trans-pyrrolidine-2,4-dicarboxylate.
5 obtained in one case with dimethyl acetylene dicarboxylate.
6  nitrogen, and 4 carboxylate of pyridine 2,4-dicarboxylate.
7 ate, but not by succinate, a nonexchangeable dicarboxylate.
8 ng buffer containing one fully (13)C-labeled dicarboxylate.
9 dehyde and methyl carbon atoms to form a 1,2-dicarboxylate.
10 hyl spiro[cycloprop[2]ene-1,9'-fluorene]-2,3-dicarboxylate.
11 onies and grew poorly on organic nitrogen or dicarboxylates.
12 ns and substrate specificity for four-carbon dicarboxylates.
13 ated that retained some ability to transport dicarboxylates.
14 2 mediate Na(+)-coupled transport of various dicarboxylates.
15 cells that shows preference for citrate over dicarboxylates.
16 a novel asymmetric alkylation of allylic gem-dicarboxylates.
17 an additional site on the enzyme for binding dicarboxylates.
18  PA5530 gene was induced by extracellular C5-dicarboxylates.
19 ,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
20 agonist APDC [(2R,4R)-4-aminopyrrolidine-2,4-dicarboxylate] (0.1 mum) or group III agonist l-(+)-2-am
21 1S,2S,5R,6S)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate 1 (LY354740) bearing C4-thiotriazole subst
22 cycloaddition of dimethyl cyclobut-1-ene-1,2-dicarboxylate (1) with cyclohexene (7) afforded two phot
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                                 Acenaphthyne dicarboxylate (12) was transferred into the gas phase fr
27          In a previous report, we discovered dicarboxylate 1a (PF-06649298) which inhibits the transp
28 ,6S-2-amino-4-methylbicyclo[3.1.0]hexane-2,6-dicarboxylate 2 (LY541850), exhibited an unexpected mGlu
29 nyl-4-phenylethynyl-1, 4-dihydropyridine-3,5-dicarboxylate (2) were obtained via an ester derived fro
30  is about 2000, releasing cyclopentanone-2,4-dicarboxylate (22) and two other precursors of this comp
31 oxylated 2E-fluoro-2,4-pentadienoate and the dicarboxylated 2E-fluoro-2-en-4-ynoate being the most po
32  syntheses of dimethyl 2,2'-bithiophene-4,4'-dicarboxylate (3), dimethyl 2,2'-bithiophene-3,4'-dicarb
33 eptor agonist (2R,4R)-4-aminopyrrolidine-2,4-dicarboxylate (3.0 microg/side) mimicked the effect of L
34  of a porous MOF, Zn(4)O(trans-4,4'-stilbene dicarboxylate)(3), with Br(2) results in diastereoselect
35 boxylate (3), dimethyl 2,2'-bithiophene-3,4'-dicarboxylate (4), and dimethyl 2,2'-bithiophene-3,3'-di
36 late (4), and dimethyl 2,2'-bithiophene-3,3'-dicarboxylate (5) are described.
37 r reaction of dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate (7) with the optically active enol ether 6
38 ethylspiro[bicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate-7,1'-cycloprop ane] (B'), A:B', and A':B;
39 diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate (8), and i-Pr2NEt and their coupling in di
40  linkers (oxalate, 6; fumarate, 8; acetylene dicarboxylate, 9; cis,cis-muconate, 11; trans,trans-muco
41 ors (X-(CH(2))(n)-X) such as alkyl dithiols, dicarboxylate acids, and alkanethiol shells capped on na
42 odeling support a model where QFR twists the dicarboxylate, activating it for catalysis.
43        In addition, p-aminohippurate and the dicarboxylates adipate and glutarate (but not succinate
44                 With SnCl4, the cyclopropane dicarboxylates afforded cyclopentene derivatives through
45 ed conditions, the alkylation of various gem-dicarboxylates afforded monoalkylated products in high y
46  binding to site IIf The decrease in matrix [dicarboxylate] allows O2 access to reduced site IIf, the
47 njugate was reduced by the OAT1-exchangeable dicarboxylates alpha-ketoglutarate, glutarate, and adipa
48 cribing the transport and assimilation of C5-dicarboxylates among bacteria.
49 of catalysis in the presence of 2,4-pyridine dicarboxylate, an analogue of alpha-ketoglutarate.
50  enzymes indicating that the ability of this dicarboxylate analogue to bridge the arginines precisely
51 old, and concomitantly decrease the K(i) for dicarboxylate analogues of l-aspartate by up to 40-fold.
52  in conjunction with di-tert-butyl hydrazine dicarboxylate and an inorganic base provides a variety o
53 ew MOF [Yb2(BDC)3(DMF)2]H2O (BDC=benzene-1,4-dicarboxylate and DMF=N,N-dimethylformamide) under solvo
54  likely orients amino acid residues near the dicarboxylate and FAD binding site, which facilitates fo
55 col utilizes a combination of an iodobenzene dicarboxylate and iodine to functionalize a series of ac
56 de at 0.6 V, whereas diethyl 2,5-dioxahexane dicarboxylate and lithium propionate form on the Sn elec
57 + 2] cycloaddition between vinylcyclopropane dicarboxylates and 3-nitroindoles has been developed.
58 inity, disulfonic stilbene-sensitive flux of dicarboxylates and citrate across the plasma membrane by
59  3a) are capable of regioselectively binding dicarboxylates and pyrophosphate (H(2)PPi(2-)).
60 DH4) contain all key residues for binding of dicarboxylates and quinones, but the enzyme showed the l
61                                              Dicarboxylates and sucrose are the main carbon sources w
62     The transporter does interact with other dicarboxylates and tricarboxylates but with considerably
63 7 ([Zr6O4(OH)4 (bpdc)6], bpdc: 4,4'-biphenyl dicarboxylate) and UiO-abdc ([Zr6O4(OH)4 (abdc)6], abdc:
64 y structures of MOFs UWDM-2 (1,4-diazophenyl-dicarboxylate) and UWDM-3 (1,4-biphenyl-dicarboxylate) s
65 not group II [(2R,4R)-4-aminopyrrolidine-2,3-dicarboxylate] and III [L-AP 4 (L-(+)-2-amino-4-phosphon
66 on of stereo- and E/Z geometric isomers of a dicarboxylate anion guest is described.
67 ne (PC), and sphingomyelin (SM) cations with dicarboxylate anions are shown to charge-invert the posi
68  studied as receptors for the recognition of dicarboxylate anions of varying chain length in aqueous
69 ape complementarity between the host and the dicarboxylate anions, which is nicely reflected in the s
70 ared to play a major role in the presence of dicarboxylate anions.
71 h respect to its ability to bind alpha,omega-dicarboxylate anions.
72 mGluR agonists (2R,4R-4-aminopyrrolidine-2,4-dicarboxylate (APDC) and L(+)-2-amino-4-phosphonobutyric
73 3)) agonists (2R, 4R)-4-aminopyrrolidine-2,4-dicarboxylate (APDC) or (2S,2'R,3'R)-2-(2'3'-dicarboxycy
74  mGluR agonist, 2R,4R 4-aminopyrrolidine-2,4-dicarboxylate (APDC), did not alter thermal sensitivity
75 es of a cooperative pinwheel chemosensor for dicarboxylates are described.
76                           To explore whether dicarboxylates are important for growth of DC3000 in the
77 indicating that transport and utilization of dicarboxylates are important for virulence of DC3000.
78                The requisite allylic geminal dicarboxylates are prepared in good yields and high isom
79 owly in culture than wild-type bacteria when dicarboxylates are the only available carbon source.
80                    High amounts of aliphatic dicarboxylates are usually considered as an indicator of
81 ) and dimethyl 3,5-dimethyl-1-pyrazoline-3,5-dicarboxylate as a specific organocatalyst has been foun
82 e yield by employing neat dimethyl acetylene dicarboxylate as the dienophile, followed by catalytic h
83 new hosts against a series of alkyl and aryl dicarboxylates as well as a range of phosphoanionic spec
84 other transcriptional regulators involved in dicarboxylate assimilation, suggesting that MifR might i
85                     Synthesis of a ruthenium dicarboxylate at a low temperature allowed for direct ob
86  transporters of dipeptides and tripeptides, dicarboxylates, auxin, and abscisic acid.
87  complex of a 1,10-phenanthroline containing dicarboxylate axle with a 1,10-phenanthroline containing
88 benzo[24]crown-8 wheels, (3) 2,6-naphthalene dicarboxylate axles with tetra-imidazolium macrocycle wh
89 ary for transport was a four-carbon terminal dicarboxylate backbone and that productive substrate-tra
90 phiphilic ligand, 4'-tert-butyl-biphenyl-3,5-dicarboxylate (BBPDC), with Zn(NO(3))(2), Co(NO(3))(2),
91 O) as axial ligands and 2,2'-bipyridine-6,6'-dicarboxylate (bda) as the equatorial ligand, we have sy
92 of nonpolar functional groups on the benzene dicarboxylate (BDC) linker in the pillared DMOF-1 [Zn2(B
93  to the conservation of amino acids near the dicarboxylate binding sites of the two enzymes is that t
94 have remarkable structural homology at their dicarboxylate binding sites.
95 odanine acetic acid) and DHP (PDC = pyridine dicarboxylate) binding sites.
96 ults in succinate-dependent reduction of the dicarboxylate-binding site of complex II (site IIf); (b)
97 nedicarboxylate (NDC), and BTE/biphenyl-4,4'-dicarboxylate (BPDC), to give four metal-organic framewo
98 mu-O)(3)Mn(IV)(tmtacn)](2+) into the active, dicarboxylate-bridged [(tmtacn)Mn(III)(mu-O)(mu-RCOO)(2)
99 esized using a salicylaldimine (sal)-derived dicarboxylate bridging ligand.
100 eptor unit 1 with several linear and angular dicarboxylate bridging ligands afforded hitherto unknown
101 highly stable MOFs (1 and 2) using elongated dicarboxylate bridging ligands derived from Cp*Ir(L)Cl c
102 y building units (SBUs) and anthracene-based dicarboxylate bridging ligands.
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                               Recognition of dicarboxylates by bis-functional hydrogen-bonding recept
107  Nitrogen-fixing rhizobial bacteroids import dicarboxylates by using the DctA transporter.
108 ([Zr6O4(OH)4 (abdc)6], abdc: 4,4'-azobenzene dicarboxylate) by single-crystal nanoindentation, high-p
109 ous DEAD reagent bis(perfluorohexylethyl)azo dicarboxylate (C(6)F(13)(CH(2))(2)O(2)CN=NCO(2)(CH(2))(2
110 byproducts from bis(perfluorohexylpropyl)azo dicarboxylate (C(6)F(13)(CH(2))(3)O(2)CN=NCO(2)(CH(2))(3
111  reagent perfluorooctylpropyl tert-butyl azo dicarboxylate (C(8)F(17)(CH(2))(3)O(2)CN=NCO2(t)Bu, F-DE
112 rapid efflux of succinate/fumarate and other dicarboxylates capable of competitively binding to site
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, couples the transp
116                                      The Na+/dicarboxylate co-transporter, NaDC-1, from the kidney an
117                                          The dicarboxylate competitive inhibitor, (2E)-fluoromuconate
118 ecedented selectivity for fum(2-) over other dicarboxylate competitors, including its cis isomer male
119                                  Rhodium(II) dicarboxylate complexes were discovered to catalyze the
120                                      The Na+/dicarboxylate cotransporter (NaDC-1) couples the transpo
121 ues, Arg-349 and Asp-373, of the renal Na(+)/dicarboxylate cotransporter (NaDC-1) have been shown in
122                                      The Na+/dicarboxylate cotransporter (NaDC1) is involved in the a
123                                      The Na+/dicarboxylate cotransporter 1 (NaDC1) is a low-affinity
124 er from Xenopus intestine and a putative Na+/dicarboxylate cotransporter from rat intestine.
125                                    The Na(+)/dicarboxylate cotransporter NaDC1 absorbs citric acid cy
126                              The human Na(+)/dicarboxylate cotransporter NaDC3 (SLC13A3) is found in
127                                    The Na(+)/dicarboxylate cotransporter transports Na(+) with citric
128 ithin the substrate access pore of the Na(+)/dicarboxylate cotransporter, either in a transmembrane h
129 s most closely related to a mammalian sodium dicarboxylate cotransporter-a membrane protein that tran
130 uctural similarity to the members of the Na+-dicarboxylate cotransporter/Na+ -sulfate cotransporter (
131                                    The Na(+)/dicarboxylate cotransporters (NaDC1) from mouse (m) and
132 aureus is a homologue of the mammalian Na(+)/dicarboxylate cotransporters (NaDC1) from the solute car
133 t sequence homology with the mammalian Na(+)/dicarboxylate cotransporters NaDC-1 and NaDC-3.
134 ily, a group that includes the mammalian Na+/dicarboxylate cotransporters NaDC1 and NaDC3.
135  the SLC13 family that also includes the Na+/dicarboxylate cotransporters, NaDC.
136 that also includes the mammalian SLC13 Na(+)/dicarboxylate cotransporters, NaDC1 and NaCT.
137 elopment of specific inhibitors of the Na(+)/dicarboxylate cotransporters.
138 [M8L12] (M=In/Cr, L=dinegative 4,5-imidazole-dicarboxylate) cubane-like structure.
139 arboxylation of nine zwitterionic pyridinium dicarboxylates (D(x,y)) are reported.
140 hoxy-5,6,5',6'-dimethylenedioxybiphenyl-2,2'-dicarboxylate (DDB) analogues were designed and synthesi
141  gene encodes 3-hydroxy-2-methylpyridine-4,5-dicarboxylate decarboxylase (HMPDdc), an enzyme involved
142 nsporter function by L-trans-pyrrolidine 2,4-dicarboxylate decreased the rate of glutamate uptake but
143 8 [(-)-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate] decreased nicotine, but not food, self-ad
144 carboxylates and 1.1 to 2.2 for alkylaminium dicarboxylates, dependent on the molecular functionality
145 cluding citrate and other tricarboxylate and dicarboxylate derivatives, this ratio ranged from 0.0003
146 -anisylformamidinate), linked by unsaturated dicarboxylate dianions of various lengths have been prep
147 conium nitrogen bond, forming a C2 symmetric dicarboxylated diazenido compound.
148                                 However, the dicarboxylate (DIC) and 2-oxoglutarate (OGC) carriers lo
149                             We also identify dicarboxylate dimers as a novel proton sensor in protein
150 otides containing complementary pyridine-2,6-dicarboxylate (Dipic) and pyridine (Py) bases.
151 rate levels, we hypothesize that by allowing dicarboxylate efflux from the matrix, PTP opening during
152  PA5530 gene in response to extracellular C5-dicarboxylates, especially alpha-KG.
153              Strikingly lower lysolipids and dicarboxylated fatty acids were seen in obese children.
154 ydrogenation of dibenzyl 5-dipyrroketone-2,9-dicarboxylates followed by decarboxylative iodination af
155 ann reaction of 2-naphthols with acetone-1,3-dicarboxylates, followed by an intramolecular Friedel-Cr
156 legans may lead to decreased availability of dicarboxylates for cellular production of metabolic ener
157 feature a new preparation of cis-cyclobutane dicarboxylates from commercially available coumalate sta
158  Thus, SdcS facilitates the transport of the dicarboxylates fumarate, malate, and succinate across th
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 rea receptors form exothermic complexes with dicarboxylates in DMSO, with a near zero entropic contri
165 ntributes to favorable binding constants for dicarboxylates in water, as well as a high degree of sel
166 ,5S,6R-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate) in adult, but not prepubertal, mice born
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 d 2) built from [Ir(ppy)(2)(bpy)](+)-derived dicarboxylate ligands (L(1) and L(2)) and Zr(6)(mu(3)-O)
179  than those of the analogous polyunsaturated dicarboxylate linked compounds and reveal at least two s
180 lt with a high-symmetry bicyclo[2.2.2]octane dicarboxylate linker in a Zn4O cubic lattice.
181 nic framework (MOF) based on a BINAP-derived dicarboxylate linker, BINAP-MOF, was synthesized and pos
182 nstructed from only bipyridyl-functionalized dicarboxylate linker, both mBPV- and mPT-MOF were built
183 , the colors upon the chemical nature of the dicarboxylate linker.
184  chemically unsaturated and fully conjugated dicarboxylate linkers (oxalate, 6; fumarate, 8; acetylen
185 /H2O ligands, subsequent insertion of linear dicarboxylate linkers is achieved.
186  alone, implying that the pi system of these dicarboxylate linkers is mediating communication.
187 tu ligand exchange with progressively longer dicarboxylate linkers is performed on single crystalline
188 3+), Yb(3+)) and linear amino-functionalized dicarboxylate linkers of different lengths.
189 I), were prepared using purely BINAP-derived dicarboxylate linkers or by mixing BINAP-derived linkers
190  BINAP-derived linkers with unfunctionalized dicarboxylate linkers, respectively.
191                         As identified by the dicarboxylate linkers, these compounds are maleate (7),
192 rved with those compounds having unsaturated dicarboxylate linkers.
193 nanthryl-functionalized and unfunctionalized dicarboxylate linkers.
194  1S,2S,5R,6S-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate (LY354740), a potent and pharmacologically
195 ds (-)-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate (LY379268, (-)-9) and (-)-2-thia-4-aminobi
196 d (-)-2-thia-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate (LY389795, (-)-10).
197  (-)-4-Amino-2-thiabicyclo-[3.1.0]hexane-4,6-dicarboxylate (LY389795, (-)-3) is a highly potent and s
198                   In contrast, the saturated dicarboxylates maintained a constant level during seed d
199 te citramalyl-CoA, an intermediate in the C5-dicarboxylate metabolic pathway that includes itaconate,
200 in the methane, pyruvate, and glyoxylate and dicarboxylate metabolic pathways.
201 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate; mmen = N,N'-dimethylethylenediamine) was
202 ive Ru-bda type (bda is 2,2'-bipyridine-6,6'-dicarboxylate) molecular OER catalysts are proposed to o
203 he hydrogen bond in hydrogen cyclohexene-1,2-dicarboxylate monoanion was determined in chloroform usi
204  (1S,2S,5R,6S-2-aminobicycl[3.1.0]hexane-2,6-dicarboxylate monohydrate) and the group III agonist L-A
205 thynyl-6-phenyl-1,4(+/-)dihydropyridine-3 ,5-dicarboxylate (MRS1191), by the phospholipase C inhibito
206 (+)]tpy-PhCOO(-)), and disodium pyridine-2,6-dicarboxylate (Na(2)pydic).
207 l2]2, tpyCOONa, and then sodium pyridine-2,6-dicarboxylate [Na(dipic)].
208  dihydrokainate, and L-trans-pyrrolidine-2,4-dicarboxylate) nor by replacement of extracellular sodiu
209 nation of dimethyl bicyclo[1.1.1]pentane-1,3-dicarboxylate, obtained from [1.1.1]propellane prepared
210 cognition elements to cooperatively bind two dicarboxylates of varying size.
211 (4-vinylpyridine)2 (bda=2,2'-bipyridine-6,6'-dicarboxylate) on planar electrodes results in films con
212                             Oxanorbornadiene dicarboxylate (OND) reagents are potent Michael acceptor
213 ixtures (> or = 81% product) of the reactive dicarboxylate or monocarboxylate intermediates, 2 or 2-h
214 ly, the GT inhibitor l-trans-pyrrolidine-2-4-dicarboxylate (PDC) potentiated, whereas the positive GT
215 ment of transport by L-trans-pyrrolidine-2,4-dicarboxylate (PDC) produced a prolongation of the decay
216 es the reversible hydrolysis of 2-pyrone-4,6-dicarboxylate (PDC) to 4-oxalomesaconate and 4-carboxy-2
217  with 100-500 microM L-trans-pyrrolidine-2,4-dicarboxylate (PDC), an inhibitor of glutamate re-uptake
218 glutamate transport: l-trans-pyrrolidine-2,4-dicarboxylate (PDC), which is a relatively non-selective
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 ponent system in response to fumarate or its dicarboxylate precursors.
223 neogenesis using deaminated amino acids with dicarboxylate products of peroxisomal lipid beta-oxidati
224 xanthenone fluorescent scaffold coupled to a dicarboxylate pseudocrown ether receptor to achieve sele
225 neutral symport reaction having a 2:1 cation/dicarboxylate ratio.
226 nd radicals generated from phenyliodine(III) dicarboxylate reagents and exhibits excellent functional
227 tamate analogue PDC (L-trans-pyrrolidine-2,4-dicarboxylate), reduced the current by approximately 88%
228 n, Co, Ni and Zn; L = 2,5-dioxidobenzene-1,4-dicarboxylate) referred to as MOF-74 and CPO-27.
229  fumarate; and the dcuSR operon encoding the dicarboxylate-responsive regulatory system.
230 ) and dimethyl 3,4-dimethylcyclopentane-1, 1-dicarboxylate (S,S-6) in 64% combined yield.
231    Saponification gave 21,23-dithiaporphyrin dicarboxylate salts 16 and 17.
232                                       The C4-dicarboxylate sensor kinase DcuS is membrane integral be
233 cur with high stereospecificity, allylic gem-dicarboxylates serve as synthons for a double allylic tr
234 enyl-dicarboxylate) and UWDM-3 (1,4-biphenyl-dicarboxylate) show that both frameworks are large enoug
235 nsa-zirconocene diiodide along with the N,N'-dicarboxylated silylated hydrazine.
236 ed in substrate binding and catalysis at the dicarboxylate site.
237 trogen fixation, although they can transport dicarboxylates, some at relatively high levels.
238 ane axle component facilitates the complexed dicarboxylate species to be sensed via a fluorescence re
239 d tetraphenylethylene and one of two benzene dicarboxylate species.
240 including the SdhE assembly factor and bound dicarboxylates, stimulate covalent flavinylation by preo
241                                   With a 1,6-dicarboxylate substrate (2-hydroxymuconate), the R61A mu
242  shows that aspartate aminotransferase binds dicarboxylate substrate analogues by bonds to Arg292 and
243 portance of Arg-11 in properly orienting the dicarboxylate substrate by interacting with the charged
244 the R11A-catalyzed protonation at C-5 of the dicarboxylate substrate decreased, while the stereoselec
245 e branched chain side chain, less so for the dicarboxylate substrate side chain.
246 ion of the protonated macrobicycles with the dicarboxylate substrates.
247 enerated a strain unable to grow on the C(4)-dicarboxylates succinate, malate, and fumarate.
248 lated a novel member of the sodium-dependent dicarboxylate/sulfate transporter called SDCT2.
249 I) lyotropic gyroid phase formed by a gemini dicarboxylate surfactant self-assembly using a combinati
250                                    The Na(+)/dicarboxylate symporter (SdcS) from Staphylococcus aureu
251                                    The Na(+)/dicarboxylate symporter from Staphylococcus aureus, name
252 pdc) (dobpdc(4-) = 4,4'-dioxidobiphenyl-3,3'-dicarboxylate) that feature step-shaped CO2 adsorption i
253 udied using a structurally similar series of dicarboxylated thiacyanine dyes that bind to the oxide s
254 on strategy, the [3]rotaxane host recognises dicarboxylates through the formation of 1:1 stoichiometr
255 boxylation of 3-hydroxy-2-methylpyridine-4,5-dicarboxylate to 3-hydroxy-2-methylpyridine-5-carboxylat
256 contribution of the polyolefinic alpha,omega-dicarboxylate to the molecular orbital undergoing oxidat
257 4'-(4-benzoate)-(2,2',2''-terpyridine)-5,5''-dicarboxylate (TPY) before being coordinated with iron c
258                                  A plastidic dicarboxylate translocator 1-[2-OG/malate translocator (
259                                          The dicarboxylate transport (Dct) system of Sinorhizobium me
260 mbrane transporters, proteins involved in C4-dicarboxylate transport and utilization, enzymes for bio
261 , consistent with the sites of high-affinity dicarboxylate transport identified based on vesicle stud
262 n and biochemical properties of bacterial C4-dicarboxylate transport systems.
263     The absence of the Arabidopsis tonoplast Dicarboxylate Transporter (tDT) in the tdt knockout muta
264  family include a Na(+)- and Li(+)-dependent dicarboxylate transporter from Xenopus intestine and a p
265 3000 in the apoplast, we disrupted the dctA1 dicarboxylate transporter gene.
266 ion that increased expression of the dctA C4-dicarboxylate transporter greatly enhanced the Cit(+) ph
267  cell motility 2), SLC13A3 (sodium-dependent dicarboxylate transporter member 3), and PREX1 (phosphat
268  function of the high affinity Na(+)-coupled dicarboxylate transporter NaDC2 in C. elegans may lead t
269                             Although the NAA dicarboxylate transporter NaDC3 is primarily thought to
270 ctural modeling using the x-ray structure of dicarboxylate transporter VcINDY as template and confirm
271 a crystal structure of Vibrio cholerae Na(+)-dicarboxylate transporter VcINDY, from which we generate
272 and Pi based on the crystal structure of the dicarboxylate transporter VcINDY.
273 d functionally characterized a Na(+)-coupled dicarboxylate transporter, SdcS, from Staphylococcus aur
274         The PA5530 gene, encoding a putative dicarboxylate transporter, was found to be essential for
275 ion of the dctA gene, which encodes the C(4)-dicarboxylate transporter, was reduced in a gyrA751 muta
276  of a mammalian Na+-dependent, high affinity dicarboxylate transporter.
277 T-PCR; the three known Na+-dependent citrate/dicarboxylate transporters could not be detected.
278                                  Other Na(+)/dicarboxylate transporters from the SLC13 family, includ
279 hila melanogaster and with the Na(+)-coupled dicarboxylate transporters NaDC1 and NaDC3 identified in
280 the differential substrate specificity among dicarboxylate transporters that underpin their diverse b
281 functionally characterized two Na(+)-coupled dicarboxylate transporters, namely ceNaDC1 and ceNaDC2,
282 cassette superfamily and telurite-resistance/dicarboxylate transporters.
283 on/Na(+) symporter (DASS) family translocate dicarboxylate, tricarboxylate or sulphate across cell me
284 ceptor cyclopropanes (2-arylcyclopropane-1,1-dicarboxylates) under double-catalysis conditions by tre
285        trans-2-Aryl-3-nitro-cyclopropane-1,1-dicarboxylates, upon treatment with BF3.OEt2, undergo ri
286 as prepared from diethyl 2-nitropyrrole-3,4,-dicarboxylate via an alkylation, ammonolysis, reduction
287 on of trans-2-aroyl-3-styrylcyclopropane-1,1-dicarboxylates was investigated with different Lewis aci
288 m catalyzed dimerization of oxanorbornadiene dicarboxylates was studied.
289 imple inorganic ions, halides, and mono- and dicarboxylates was taken into account.
290  hydroxamates derived from trans-cyclopropyl dicarboxylate were examined as potential TNF-alpha conve
291 he alkylation of di-tert-butyl hydrazine-1,2-dicarboxylate were investigated.
292                A wide variety of oxetane 2,2-dicarboxylates were accessed in high yields, including f
293                                        These dicarboxylates were found predominantly in epidermal pee
294 f 4-oxo-2,4-dihydrocyclopenta[c]chromene-1,2-dicarboxylates were obtained in moderate to good yields
295                       The m- and p-carborane dicarboxylates were utilized as the donor linkers in con
296    Asymmetric alkylations of allylic geminal dicarboxylates with dialkyl malonates have been investig
297 nding is observed for dicarboxylic acids and dicarboxylates with four-carbon chains, and the binding
298         The ring-opening of cyclopropane-1,1-dicarboxylates with vicinal donor aryl groups by boronic
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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