「ligands」の共起表現一覧(1語右で並び替え)2ページ目
該当件数 : 277件
pite the large amount of processes that these | ligands regulate, they all operate through essentiall |
small crown ether) and cyclopentadienyl (Cp) | ligands related ligands and form related complexes. |
Other | ligands replacing the oxide ions have also been attes |
Fe3(CO)12 is different, with two bridging CO | ligands resulting in C2v symmetry. |
CXCR4 alpha-chemokine receptor and one of its | ligands, SDF-1, are important in hematopoietic stem c |
of chemical compounds which are tetradentate | ligands similar in shape to quaterpyridine. |
The macromolecule is assumed to bind to n | ligands simultaneously (where n is to be determined) |
y, is degraded by, aqueous solutions of basic | ligands such as hydroxide, ammonia, and additional cy |
ve been shown to bind different substances or | ligands such as sterols (e.g., StAR or STARD1) and li |
Binding study using various | ligands such as antibodies, lectins, bacterium, virus |
es are even known containing purely inorganic | ligands, such as Fe(C5Me5)(P5) and [(P5)2Ti]2-. |
the possibility of tripodal heptadentate | ligands such as N4O3 from the ligand tris[6-((2-N,N-d |
Polyatomic | ligands such as carbonate are ambidentate and thus ar |
ressed in cells of the immune system and bind | ligands such as CD55. |
s also useful for detecting interactions with | ligands, such as other proteins or drugs. |
of CNS-related side effects than hydrophilic | ligands such as atenolol, sotalol and nadolol. |
Studies of this receptor and its | ligands suggested its role in regulation of monocyte |
In other words, some | ligands tend to turn the receptor on and some tend to |
emical specificity, a measure of the types of | ligands that will bond, and affinity, which is a meas |
Crown ethers are not the only macrocyclic | ligands that have affinity for the potassium cation. |
llic compound containing two cyclopentadienyl | ligands that are linked by a bridging group such that |
This diamine is a building block for chiral | ligands that are useful in asymmetric catalysis. |
x coordination sites are occupied by fluoride | ligands that bridge to adjacent Cr centres. |
nes function as planar tetradentate dianionic | ligands that bind metals through four inwardly projec |
it had developed a library of small chemical | ligands that bind to dengue virus envelope proteins. |
etal is reduced by any negative charge on the | ligands, the d-orbitals can expand slightly. |
Upon binding to 17-β-estradiol or related | ligands, the encoded protein forms homo-dimers or het |
With two THF | ligands the catalyst is stable but in dichloromethane |
omplex's metal atom structures and the olefin | ligands themselves can conduct a current. |
eadily dissociates one of the three phosphine | ligands, thereby generating a reactive 16-electron co |
sponse to signals by the TGF-β superfamily of | ligands these proteins associate with receptor kinase |
is surrounded by an octahedron of six iodide | ligands, three of which are closer and three more dis |
signals from transforming growth factor beta | ligands to the nucleus where they activate downstream |
d Cys6) and backbone nitrogen (His1 and Cys2) | ligands, to square pyramidal Ni(III) with an added ax |
n arrangement is for the so-called equatorial | ligands to lie in a plane perpendicular to the O-U-O |
s, the four central nitrogen atoms can act as | ligands to bond to a metal ion in the center of the m |
ning of small molecule databases of candidate | ligands to identify novel small molecules that bind t |
bind to one two-electron or two one-electron | ligands to become electronically saturated with 18 va |
Binding of agonist | ligands to RAR results in dissociation of corepressor |
Binding of agonist | ligands to RXR results in dissociation of corepressor |
ordering roughly reflects the ability of the | ligands to form good covalent bonds with metals - tho |
torically, receptors were discovered by using | ligands to "fish" for their receptors. |
Enedithiolates displace all four chloride | ligands to give bis(dithiolene) complexes. |
etry of ladderanes is highly strained because | ligands to the carbon atoms cannot extend to their id |
One of the most active areas of search for | ligands to receptors, are in the field of brain recep |
nd is readily substituted with other stronger | ligands, to give linear gold bromide complexes. |
Back-electron transfer from the | ligands to the metal after the charge transfer, which |
FT is frequently used to map binding of novel | ligands to the DAT, although the drug also has some S |
Binding of a subgroup of TGFβ superfamily | ligands to extracellular receptors triggers phosphory |
nary complex formed between two identical FGF | ligands, two identical FGFR subunits and either one o |
tly, the molecule has two distinct types of F | ligands, two axial and two equatorial. |
As with other peptide | ligands, U-II is synthesised from a larger precursor |
, but they do not adhere to their appropriate | ligands until the leukocytes are activated by chemota |
ine solid tends to hydrolyse and lose ammonia | ligands upon standing in air. |
arious members of the TGF-beta superfamily of | ligands via its core protein, and bFGF via its hepara |
oring biological activity of nuclear receptor | ligands', Volume 16, Issue 2, Mar-Apr 2001, Pages: 15 |
A set of | ligands were evaluated. |
Phenanthroline | ligands were first published in the late 19th century |
he nuclear receptor superfamily because their | ligands were unknown. |
expression pattern of Eph receptors and their | ligands, which is vital to proper segmentation - the |
develop several more specialised cannabinoid | ligands which are now widely used in research, includ |
-derived neurotophic factor (GDNF ) family of | ligands which are a group of ligands within the TGF-b |
Recent research has produced several | ligands which are moderately selective for GABAA rece |
main of an Eph receptor interacts with ephrin | ligands, which may be tethered to neighbouring cells. |
abotropic receptors have neurotransmitters as | ligands, which, when bound to the receptors, initiate |
Synthetically, this may be achieved by using | ligands whose geometries prevent the metal from being |
t forms roughly equally strong complexes with | ligands whose donor atoms are N, O or F as with ligan |
Ligands with desired parameters can be selected from | |
roup found in many indole derived cannabinoid | ligands, with an adamantoyl group, generally confers |
Based on the 2:1 complexes were obtained | ligands with high sequence-selectivity. |
Upon "treatment" of the | ligands with (H2O2 + AcOH) the sulfur atom is oxidize |
is commonly used to replace halide anions or | ligands with the weakly-coordinating tetrafluoroborat |
e displacement of the bridging isothiocyanate | ligands with the incoming alcohol to form an alcohol- |
tion results from strain caused by binding to | ligands with relative orientation that is pre-arrange |
Antagonist | ligands work by inducing a conformation of the recept |
other nickel(II) derivatives where the water | ligands would be replaced. |
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