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「THIOL」の共起表現一覧(1語右で並び替え)

該当件数 : 57



unstable because they readily dissociate into thiol and aldehyde.
This thiol appears to participate in the sensing of perox
cysteine residue, in the presence of an added thiol catalyst.
In 1985, Alan Fairlamb discovered a unique thiol compound present in these parasites, and named
ycothiol (MSH or AcCys-GlcN-Ins) is an unusual thiol compound found in the Actinobacteria.
Bacillithiol (BSH or Cys-GlcN-mal) is a thiol compound found in Bacillus species.
icin is greatly accelerated in the presence of thiol compounds.
e synthases (or synthetases) in an energy-rich thiol ester linkage.
the growing chain bound during synthesis as a thiol ester at the distal thiol of a 4'-phosphopante
cinic acid is a dicarboxylic acid containing a thiol functional group.
olving a nucleophilic attack of the N-terminal thiol group of peptide 2 at the α-thioester of pepti
ould it be possible to use chains containing a thiol group for the R and R' so that disulfide bridg
teine occurs via nucleophillic attack from the thiol group of the cysteine on C2 of the epoxide.
ation is the cleavage of 3-ketoacyl CoA by the thiol group of another molecule of CoA.
l, in the presence of water) specifically at a thiol group.
on in which mercury replaces a nitrosyl from a thiol group.
reduced form of the protein contains two free thiol groups at the cysteine residues, whereas the o
At neutral pH, protein thiol groups specifically react with the functional
e exchange reactions that oxidise the cysteine thiol groups of nascent polypeptides.
Activity is mediated by the two thiol groups that the molecule contains.
PCMB reacts with thiol groups in proteins and is therefore an inhibit
Dimercaprol competes with the thiol groups for binding the metal ion, which is the
is also used in titrimetric quantification of thiol groups in proteins.
It binds to metal cations through the thiol groups, which ionize upon complexation.
f nitric oxide; it refers to the conversion of thiol groups, including cysteine residues in protein
Hg2+ ions bind to thiol groups.
ists of a benzene ring with a pair of adjacent thiol groups.
hydroxy group of terpineol is replaced by the thiol in grapefruit mercaptan, so it also called thi
echanism that involves a nucleophilic cysteine thiol in a catalytic dyad.
was first detected in 2007, as an unidentified thiol in Bacillus anthracis.
The first step is deprotonation of a thiol in the enzyme's active site by an adjacent ami
The thiol is susceptible to oxidization to give the disu
The thiol is inserted between C-2 and C-3, which yields
boxy-terminus of the substrate to the cysteine thiol is formed.
This thiol is used as a flavoring agent and used in a wid
This thiol metabolite is quite different from its human e
Butanethiol is a thiol of low molecular weight, and it is highly flam
In enzymology, a thiol oxidase (EC 1.8.3.2) is an enzyme that catalyz
erefore they are also sometimes referred to as thiol proteases.
etals act by chemically reacting with adjacent thiol residues on metabolic enzymes, creating a chel
The thiol reversibly interacts with a zinc atom in the b
The thiol side chain often participates in enzymatic rea
e enzyme and serves as a disfulfiram sensitive thiol site.
it is likely that the very vile nature of the thiol starting material is likely to make the synthe
albumin, insulin, transferrin, selenium and a thiol such as 2-mercaptoethanol or 1-thioglycerol
In enzymology, a thiol sulfotransferase (EC 2.8.2.16) is an enzyme th
al reactions, including the addition of benzyl thiol, the coupling of enolates, and stereospecific
hemithioacetal can be prepared by addition of thiol to methyl glyoxalate.
these enzymes by over-oxidation of the active thiol to sulfinic acid can be reversed by sulfiredox
iredoxin-(S-hydroxy-S-oxocysteine), ATP, and a thiol, whereas its 4 products are peroxiredoxin-(S-h
this enzyme are 3'-phosphoadenylyl sulfate and thiol, whereas its two products are adenosine 3',5'-
The side chain on cysteine is thiol, which is nonpolar and thus cysteine is usuall
The molecule contains a thiol, which is its principal site of reaction.
Mercaptoethanesulfonate contains both a thiol, which is the main site of reactivity, and a s
, sometimes called 1,2-dimercaptopropane, is a thiol with the formula HSCH2CH(SH)CH3.
An alternative reaction is the reaction of a thiol with P4S10 to form a substance like the Davy r
                                                                                                   


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