「ligands」の共起表現(2語左で並び替え) - Weblio英語共起表現検索


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「ligands」の共起表現一覧(2語左で並び替え)

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s, the four central nitrogen atoms can act as ligands to bond to a metal ion in the center of the m
in which three bidentate oxalate ions act as ligands bound to an iron centre.
ts as a transducer of activin or activin like ligands (e.g., inhibin) signals.
of Various New Aryl and Aryl Alkyl Phosphane ligands”.
homoleptic complex, which means that all the ligands are the same.
(See also Chemotaxis#Chemotactic ligands.)
ordination complexes of dppe, and diphosphine ligands in general, are almost entirely used as homog
a high degree of structural homology and few ligands are available that can distinguish between th
d Cys6) and backbone nitrogen (His1 and Cys2) ligands, to square pyramidal Ni(III) with an added ax
atinum(0) compounds contain alkene and alkyne ligands.
etween the central metal ion and polypyridine ligands are usually very strong; furthermore, the pol
ycoforms that serve as P-, L-, and E-selectin ligands and fibrin, but not fibrinogen, receptors und
expression pattern of Eph receptors and their ligands, which is vital to proper segmentation - the
arch on cobalt complexes of salen and related ligands for their capacity for oxygen storage and tra
um atoms are bridged by both CH2 and chloride ligands.
ter to hard bases such as oxygen and nitrogen ligands, copper(I) is normally tetrahedral and binds
Studies of this receptor and its ligands suggested its role in regulation of monocyte
ressed in cells of the immune system and bind ligands such as CD55.
ive oxidation states with oxygen and fluorine ligands.
Free cyano and carbonyl ligands are toxic to many biological systems so their
le ribosome in complex with its tRNA and mRNA ligands.
h the displacement of the cod and/or chloride ligands.
is commonly used to replace halide anions or ligands with the weakly-coordinating tetrafluoroborat
ks the binding of the antigen-presenting cell ligands B7.1 and B7.2 to CTLA-4, resulting in inhibit
c properties of phosphines, which are popular ligands for catalysts.
ese zwitterionic teichoic acids are suspected ligands for toll-like receptors 2 and 4. Teichoic aci
of chemical compounds which are tetradentate ligands similar in shape to quaterpyridine.
, involving interaction with a large array of ligands.
he dissolved copper(II) sulfate, as bidentate ligands giving the bistartratocuprate(II)4- complex a
They have also been identified as potential ligands for radioisotope delivery, with selectivity t
have an equally good claim to be scorpionate ligands.
cellular adhesion to other cells bearing its ligands, CD112 and CD155, and cross-linking CD226 wit
he nuclear receptor superfamily because their ligands were unknown.
Kisspeptins behave as ligands for the G-protein-coupled receptor, GPR54 (21
The best-known PPAR ligands are the thiazolidinediones; see below for mor
An equilibrium exists between unbound ligands and bound ligands.
g Na+ centers sandwiched between μ-η5:η5-C5H5 ligands.
Related bidentate phosphine-containing ligands derived from other chiral diamines have also
urally distinct families which bind different ligands and are primarily expressed in different tiss
nstead of being activated by binding chemical ligands like their relatives, rhodopsins contain reti
tion results from strain caused by binding to ligands with relative orientation that is pre-arrange
Removal of the two bound chloride ligands from [VCl2(H2O)4]+ in aqueous solution gives
and properties of adamantane bridged diimine ligands and their Ru(II) and Os(II) complexes" under
al aluminium centers sharing bridging hydride ligands.
Fe3(CO)12 is different, with two bridging CO ligands resulting in C2v symmetry.
e displacement of the bridging isothiocyanate ligands with the incoming alcohol to form an alcohol-
nters are linked by four bridging carboxylate ligands.
Related bulky anionic ligands include C5Me5-, (Me3Si)2N-, and NacNac-.
hem are capable of being shut off by chemical ligands even though they do not require ligands in or
ocess involving first activation by microbial ligands, followed by binding of an rNTP to the nucleo
ntains three platinum centres linked by amine ligands.
Synthetically, this may be achieved by using ligands whose geometries prevent the metal from being
eceptors can be excited by neurotransmitters ( ligands) like glutamate and aspartate.
nitude of the splitting energy exerted by the ligands on d orbitals, as a free ion approach a ligan
It functions by stimulating ligands for interleukin 3 and c-Mpl.
torically, receptors were discovered by using ligands to "fish" for their receptors.
pied by water, which can be replaced by other ligands.
x coordination sites are occupied by fluoride ligands that bridge to adjacent Cr centres.
onsisting of metal centres linked by bridging ligands.
ligand which is easily displaced by stronger ligands like triphenylphosphine, hence it serves a us
e others are activated by Ca2+, extracellular ligands, and pH among other modulators.
tidyinositol-linked protein that captures its ligands from the extracellular milieu and transports
d extensively with N-heterocyclic carbenes as ligands.
In it, two carbon monoxide ligands and three triphenylphosphine ligands are coor
g a signalling cascade through certain ephrin ligands.
lves only upon breaking the chloride bridging ligands.
d therapeutic agents over classic orthosteric ligands.
and ions-in this context collectively called ligands, or more specifically, protein ligands-form a
ransition metal free ion forms a complex with ligands.
solvent, for example, complex-forming anions ( ligands) in liquids.
t forms roughly equally strong complexes with ligands whose donor atoms are N, O or F as with ligan
Complexes containing η2-O2 ligands are fairly common, but most are generated usi
duced to neutral derivatives containing bipy- ligands.
Important compounds containing P(Cy)3 ligands include the 2005 Nobel Prize-winning Grubbs'
As the coordinated acetonitrile ligands may be displaced in other solvents, the [Cu(C
small crown ether) and cyclopentadienyl (Cp) ligands related ligands and form related complexes.
Unlike most other D2 receptor ligands, piquindone displays Na2+-dependent binding,
roup found in many indole derived cannabinoid ligands, with an adamantoyl group, generally confers
The group designed new ligands for complexation of iron and aluminium, techn
eptors have the capacity to detect endogenous ligands, and certain fatty acid amines that arise fro
Because the dibutyl phosphate ligands are acidic, it will now be possible to extrac
ls, with their ability to gather & dispose of ligands in a given predictable geometry, can induce a
tions of proteins with radiolabeled DNA, RNA, ligands, and other small chemicals.
s octahedral, with oxo, four equatorial water ligands, and a monodentate sulfate.
f which bears two axial and two equatorial CO ligands.
equivalently, SELEX (systematic evolution of ligands by exponential enrichment) to bind to various
from salicylaldehyde, are excellent chelating ligands.
soft and hard-hard interactions exist between ligands and metal centers.
signals from transforming growth factor beta ligands to the nucleus where they activate downstream
modulation of transforming growth factor beta ligands.
The B7 family is a family of ligands.
-derived neurotophic factor (GDNF ) family of ligands which are a group of ligands within the TGF-b
dinated to two Tc neighbors and five chloride ligands (Tc-Tc bond length 2.44 angstrom).
planar, consistent with VSEPR theory for four ligands and two lone pairs (or AX4E2 in the notation
Activation ligand for other ligands bound to that metal.
rapeutic roles have been suggested for 5-HT5A ligands due to the presence of this receptor in sever
This diamine is a building block for chiral ligands that are useful in asymmetric catalysis.
nd type II receptors are required for binding ligands and for expression of type I receptors.
nd type II receptors are required for binding ligands and for expression of type I receptors.
any cases there are more than four equatorial ligands.
Enedithiolates displace all four chloride ligands to give bis(dithiolene) complexes.
two metal atoms are bridged by four bidentate ligands.
Back-electron transfer from the ligands to the metal after the charge transfer, which
It condenses with amines to give diketimines ligands.
mercaptoethylamines, which are good chelating ligands.
vation by a subset of potential growth factor ligands.
to better assess the activity of H3 receptor ligands.
pe I integral membrane receptor that has many ligands, including the cyclophilin (CyP) proteins Cyp
s well as certain peptides, are high affinity ligands for the lipoxin A4 receptor (LXA4R), which wa
t is motivated by the inclusion of high field ligands like cyano and CO (metal carbonyl) in the fir
These high field ligands may ensure the iron centers at the active sit
Few highly selective ligands are commercially available for the 5-HT5A rec
ylaminotetralins are novel histamine receptor ligands.
nary complex formed between two identical FGF ligands, two identical FGFR subunits and either one o
urring compounds that have been identified as ligands of Ahr include derivatives of tryptophan such
arbohydrate specificity and identify specific ligands.
If other ligands increase the density of π electrons on the me
mbles some biologically important macrocyclic ligands, as found for example in vitamin B12 and myog
interacting with sialic acid molecules in the ligands on their surfaces.
oximes are commonly utilized in metallacrown ligands.
s also useful for detecting interactions with ligands, such as other proteins or drugs.
G/PMA-binding domain binds two zinc ions; the ligands of these metal ions are probably the six cyst
has been refined to include less symmetrical ligands of the type PRR'R" as well as diphosphines.
oordinated to four almost linear acetonitrile ligands in a nearly ideal tetrahedral geometry.
ine solid tends to hydrolyse and lose ammonia ligands upon standing in air.
While many scorpionate ligands are of the Tp class, many other scorpionate l
Many related ligands can be prepared from other diketones, e.g.
-COO- linkage - a parent compound of many MAT ligands (here in a unfavourable conformation of the O
mily of extracellular signalling molecules or ligands (GFLs).
ytokines, cell adhesion molecules, receptors, ligands, and enzymes.
te Sb(OAc)3 monomers with monodentate acetate ligands.
ramidites are also used as monodentate chiral ligands in asymmetric synthesis.
so is much less selective than most research ligands, but as of 2009 no superior 5-HT2B agonist is
osely related 5-HT1B receptor, and most older ligands for these receptors bind to both subtypes wit
y virtue of the presence of multiple bridging ligands.
unds have been used as N-heterocyclic carbene ligands on various transition metals.
fluoride complexes of N-heterocyclic carbene ligands.
abotropic receptors have neurotransmitters as ligands, which, when bound to the receptors, initiate
ide, with each Ba center bound to nine iodide ligands.
oring biological activity of nuclear receptor ligands', Volume 16, Issue 2, Mar-Apr 2001, Pages: 15
Other synthetic nuclear receptor ligands have no apparent effect on gene transcription
ntate, tridentate characterized the number of ligands attached to a metal.
neration and selection of the large number of ligands for high-throughput screening.
A number of ligands have been found to bind to various sites on t
CXCR4 alpha-chemokine receptor and one of its ligands, SDF-1, are important in hematopoietic stem c
Efficacy spectrum of receptor ligands.
anic synthesis as well as a source of diverse ligands and building blocks for researchers.
e indenyl effect, the reaction of coordinated ligands, and synthetic models for myoglobin.
e(NO)2 units are bridged by a pair of sulfide ligands.
y, is degraded by, aqueous solutions of basic ligands such as hydroxide, ammonia, and additional cy
More recently a range of selective ligands for ORL-1 have been developed, which show lit
The binding site of endogenous ligands on LGICs protein complexes are normally locat
ning of small molecule databases of candidate ligands to identify novel small molecules that bind t
n be used in the synthesis of organophosphine ligands for transition metal catalysis.
he graph correspond to pseudorotations of the ligands.
s commonly used in the synthesis of phosphine ligands.
Binding of agonist ligands to RAR results in dissociation of corepressor
Binding of agonist ligands to RXR results in dissociation of corepressor
A large group of such ligands is derived from the chiral diol BINOL and can
tly, the molecule has two distinct types of F ligands, two axial and two equatorial.
affinity chromatography by use of immobilized ligands.
Upon "treatment" of the ligands with (H2O2 + AcOH) the sulfur atom is oxidize
ordering roughly reflects the ability of the ligands to form good covalent bonds with metals - tho
rahedral centers linked by a pair of bridging ligands.
describes the enhanced affinity of chelating ligands for a metal ion compared to the affinity of a
The chemical structures of the ligands are Ca+2 ion, alpha-D-mannose (C6H12O6), and
ation of biosorbents and the use of selective ligands for metal sorption.
includes formation of cyclopentadienone-like ligands.
sed for high-throughput screening of receptor ligands and calcium permeable ion channels.
The number of characterized ligands in the TGFβ superfamily far exceeds the numbe
with good yields by displacement of pyridine ligands of the trispyridine complex Mo(CO)3(pyridine)
sing different pyrazoles a range of different ligands can be formed.
dinating solvents or in the presence of donor ligands.
FT is frequently used to map binding of novel ligands to the DAT, although the drug also has some S
earch Article: 'Automated docking of flexible ligands: Applications of AutoDock', Volume 9, Issue 1
etal is reduced by any negative charge on the ligands, the d-orbitals can expand slightly.
Crown ethers are not the only macrocyclic ligands that have affinity for the potassium cation.
f a coordination complex bearing only hydride ligands.
s by rats distinct from other opioid receptor ligands, but was not able to produce the conditioned
TLR) or microbial ligands.
Upon binding to 17-β-estradiol or related ligands, the encoded protein forms homo-dimers or het
enes using dihydroquinine or dihydroquinidine ligands on an osmium metal center
and Ang4 function as agonistic or activating ligands for Tie2, whereas Ang2 and Ang3 behave as com
etal ions linked together by organic bridging ligands and are a new development on the interface be
As with other peptide ligands, U-II is synthesised from a larger precursor
main, and includes several other non-cytokine ligands like CD40, CD27 and CD30, besides the ligands
cell adhesion molecules with other recognized ligands before their HA binding was discovered.
nd is readily substituted with other stronger ligands, to give linear gold bromide complexes.
h palladium complexes of most other phosphine ligands.
Other C2-symmetric ligands derived from trans-1,2-diaminocyclohexane (DA
werful therapeutic advantage over orthosteric ligands, namely the ability to selectively tune up or
lization and specificity for particular lipid ligands.
to nitrogen, oxygen or phosphorus containing ligands, although stabilization can be achieved throu
energetic consequences of pre-organization of ligands in their biologically active conformation is
cell populations or study preference between ligands.
Recent research has produced several ligands which are moderately selective for GABAA rece
f Toll-like receptor related products (mainly ligands and engineered mammalian cell lines), selecti
es are even known containing purely inorganic ligands, such as Fe(C5Me5)(P5) and [(P5)2Ti]2-.
puter database to track the reaction rates of ligands and how they react with ions to form complex
                                                                                                   


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