「INHIBITORS」の共起表現(1語右で並び替え)

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共起表現

「INHIBITORS」の共起表現一覧(1語右で並び替え)

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MAO), which is a target of monoamine oxidase	inhibitors, a class of antidepressants.
adol also function as noradrenaline reuptake	inhibitors, a property that contributes to their overal
nown to act as selective monoamine oxidase A	inhibitors, a side effect which can lead to lethal sero
Sheddase	inhibitors active on ADAM10 and ADAM17 can potentiate a
Chitin synthesis	inhibitors affect insects for longer periods of time th
ALS	Inhibitors affect grasses and dicots by inhibiting the
has led to the synthesis of highly specific	inhibitors against a number of protein kinases, includi
Some haemophiliacs develop antibodies (	inhibitors) against the replacement factors given to th
These	inhibitors also inhibit PDK1 explaining the higher inhi
The use of	inhibitors also decreases the localized zones of high p
alled specialty pharmaceuticals (such as TNF	Inhibitors) also use coupons as a marketing tactic.
ding conformation changes in serine protease	inhibitors, also known as serpins, mutations of which a
With these	inhibitors, an insect grows normally until it molts.
They are broad spectrum	inhibitors and are chemically diverse with different ty
is a member of the serpin family of protease	inhibitors, and participates in DNA and chromatin conde
s an adjunct to conventional treatments (ACE	inhibitors and diuretics).
breast cancer (in combination with aromatase	inhibitors) and for metastatic lung cancer (in combinat
hography and process engraving; in corrosion	inhibitors; and in pharmaceutical preparations.
Proton Pump	Inhibitors and C-Difficile
The effect of diuretics, ACE	inhibitors and angiotensin II receptor antagonists can
es, best known of which is azoxystrobin; QoI	inhibitors) and as anti-malaria agents (atovaquone).
strong serine/threonine protein phosphatase	inhibitors and based on this property, calyculins might
Other ingredients include corrosion	inhibitors and flow conditioners.
viruses that are resistant to other protease	inhibitors and it recommended for patients who are resi
The fluoroquinolones are known as GABA	inhibitors and as such have the ability to bind to neur
ste management, biologically active protease	inhibitors, and chemically inert redox shuttles for dye
ilar in concept to the use of selective MAOA	inhibitors and selective MAOB inhibitors in augmentatio
side the brain, to form two selective enzyme	inhibitors and blocking both types of the zinc-metallop
clude peroxidase, acid phosphatase, protease	inhibitors, and calcium.
The class I bacteriocins are small peptide	inhibitors and include nisin and other lantibiotics.
emely toxic at low levels, both are Na+ pump	inhibitors and both have nearly identical binding const
tituted phenyltropanes are highly potent MAT	inhibitors and also have a very long half-life, spannin
for screening transporter substrates and/or	inhibitors; and also to determine in vitro drug resista
diet and various medications especially ACE	inhibitors and angiotensin receptor blockers can lower
nidate both in efficacy as dopamine reuptake	inhibitors and in animal drug discrimination assays.
letal toxicity in the case of broad spectrum	inhibitors) and failure to show expected results (in th
blishes new knowledge and findings on enzyme	inhibitors and inhibitory processes as well as agonist/
ese drugs are known as reverse transcriptase	inhibitors and include the nucleoside and nucleotide an
blood pressure (antihypertensive drugs): ACE	inhibitors, angiotensin receptor blockers, α blockers,
Some JAK2	inhibitors are under development for the treatment of p
Trypsin	inhibitors are chemicals that reduce the availability o
If anodic	inhibitors are used at too low concentration, they can
Some corrosion	inhibitors are hexamine, benzotriazole, phenylenediamin
ed levels of this enzymatic activity, though	inhibitors are in development and clinical trials.
Kinase	inhibitors are low molecular weight molecules that prev
Alpha-glucosidase	inhibitors are used to establish greater glycemic contr
Many serpins (serine protease	inhibitors) are metastable, and undergo a conformationa
COMT	inhibitors are used in the treatment of Parkinson's dis
Some IGR-1R	inhibitors are in various stages of development (based
Thromboxane synthase	inhibitors are used as antiplatelet drugs.
RORγt	inhibitors are under development for autoimmune disease
Many HDAC	inhibitors are potential treatments for cancer through
Some glycosyltransferase	inhibitors are of use as drugs or antibiotics.
g on September 4, 2008, that patients on TNF	inhibitors are at increased risk of opportunistic funga
Some P2Y12	inhibitors are used clinically as effective inhibitors
Alpha-glucosidase	inhibitors are saccharides that act as competitive inhi
Other substitutents of these	inhibitors are usually designed to interact with variou
Several prolyl endopeptidase	inhibitors are known, and have been suggested as possib
Pyrimidine synthesis	inhibitors are used in active moderate to severe rheuma
Along with carbidopa, other DDC	inhibitors are benserazide (Ro-4-4602), difluromethyldo
Xanthine oxidase	inhibitors are being investigated for management of rep
Xanthine oxidase	inhibitors are of two kinds: purine analogues and other
Allosteric serotonin reuptake	inhibitors are therefore not a therapeutically distinct
A large number of AChE	inhibitors are used in both medicine and agriculture.
Integrase	inhibitors are a class of antiretroviral drug designed
ve bacteria, and synthetic versions of these	inhibitors are in clinical trials for the prevention of
Early results from clinical trials of PARP	inhibitors are considered to be important and promising
Thus, while ACE	inhibitors are still considered first-line therapy in h
For this reason, several FTase	inhibitors are undergoing testing as anti-cancer agents
ly SNRIs (serotonin-norepinephrine re-uptake	inhibitors), as this increases the risk of the above sy
More recently a new series of renin	inhibitors based on the ketopiperazine structure was de
Two angiogenesis	inhibitors based on Dr. Folkman's hypothesis and develo
of nucleoside analogue reverse transcriptase	inhibitors, because DNA production by reverse transcrip
Both	inhibitors bind with high affinity and specificity, and
Most TCAs act as reuptake	inhibitors, but opipramol does not, and instead acts as
does not produce nearly as many fermentation	inhibitors but must be separated from the sugar stream
ltramadol are inactive as serotonin reuptake	inhibitors, but (-)-O-desmethyltramadol retains activit
hibited by hirudin and other direct thrombin	inhibitors, but not by heparin.
go a chemical reaction and can act as enzyme	inhibitors by blocking their active site.
While Novartis was developing	inhibitors by modification of the peptide-like inhibito
tose intolerance or the use of α-glucosidase	inhibitors by diabetics), gluten (protein in wheat, bar
raig Jordan and initial studies of aromatase	inhibitors by 2005 Kettering prize recipient Angela Bro
OPS online database for peptidases and their	inhibitors: C01.032
After some time, though, some	inhibitors can develop a permanent bond with cholineste
Therapeutic ADAM	inhibitors can potentiate anti-cancer therapy.
Angiotensin-converting enzyme (ACE)	inhibitors can also be used.
s, particularly injectable drugs such as TNF	inhibitors can be worth several thousands of dollars pe
Chitin synthesis	inhibitors can also kill eggs by disrupting normal embr
	Inhibitors can escape removal during the DNA purificati
Protease	inhibitors changed the very nature of the AIDS epidemic
r (sedative which contains monoamine oxidase	inhibitors), Citrus aurantium (contains small amounts o
f resins, waxes, nylons, plastics, corrosion	inhibitors, coatings, lubricating greases and cosmetics
Although aromatase	inhibitors could be considered antiestrogens by some de
with the older non-selective cholinesterase	inhibitors currently used for this application, such as
Specific	inhibitors developed using rational design have recentl
Conventional protease	inhibitors do not completely inactivate Factor I but th
he Cybermen by shutting down their emotional	inhibitors, enabling them to "see" what had become of t
devoted to the development of protein kinase	inhibitors, especially tyrphostins/TKIs.
by the use of diuretics, beta blockers, ACE	inhibitors, etc., or to repair/replace the mitral valve
tanning leather, antiperspirants, corrosion	inhibitors, extraction of uranium, petroleum refining,
ated that he had studied proteases and their	inhibitors for twenty years.
been conducted on everolimus and other mTOR	inhibitors for use in a number of cancers.
, A. The Potential Role of Serine Proteinase	Inhibitors for the Prevention of Plaque Rupture.
There are three classes of commonly used	inhibitors for metalloproteinases.
caution should be used when prescribing PDE5	inhibitors for erectile dysfunction for patients receiv
semide) and UV-absorber as well as corrosion	inhibitors for metals and mold inhibitors in soya sauce
They have also been used as specific	inhibitors for various enzymes.
ug have been developed as CYP2C9 and CYP2C19	inhibitors for use in research.
As well as methods for the removal of	inhibitors from samples before PCR, some DNA polymerase
It also contains a group of proteinase	inhibitors from the plants Arabidopsis thaliana and Bra
Synthetic	inhibitors generally contain a chelating group which bi
e solution in the presence of polymerization	inhibitors gives crude chloroprene.
A number of rationally designed MMP	inhibitors have shown some promise in the treatment of
nger popular as many orally active aromatase	inhibitors have been identified.
Some Akt	inhibitors have undergone clinical trials.
ct primarily as selective serotonin reuptake	inhibitors have also been found to increase the levels
Zinc finger	inhibitors have been tested for their efficacy in treat
terference that selective serotonin reuptake	inhibitors have on serotonergic psychedelic drugs.
seeds and various serine proteases and their	inhibitors have been determined by his group.
FTase	inhibitors have shown efficacy as anti-parasitic agents
Competitive	inhibitors have the same y-intercept as uninhibited enz
Acetylcholinesterase	inhibitors, highly toxic to other animals and humans, a
OPS online database for peptidases and their	inhibitors: I04.001
OPS online database for peptidases and their	inhibitors: I04.033
Beta-lactamase	inhibitors in clinical use include clavulanic acid and
urrently one of the furthest advanced PDE10A	inhibitors in development and has progressed through to
se of atropine along with anticholinesterase	inhibitors in order to prevent side effects.
blasts, suggesting a potential role for PDE7	inhibitors in the treatment of osteoporosis.
among the tropane-derived dopamine reuptake	inhibitors in that the active stereoisomer is the (S) e
The global market for TNF	inhibitors in 2007 was $10Bn, and in 2008 it was $13.5B
te a dissertation entitled Monoamine oxidase	inhibitors in Amazonian hallucinogenic plants: ethnobot
t the NYU School of Medicine using synthesis	inhibitors in psychiatric patients responding to antide
Exogenous matrix metalloproteinase	inhibitors include batimastat and marimastat.
COMT	inhibitors include tolcapone and entacapone, which are
Other	inhibitors include 2-phosphoglycolate, a transition sta
es of drugs that are transition state analog	inhibitors include flu medications such as the neuramin
HMG-CoA reductase	inhibitors including simvastatin, simvastatin acid, lov
omologous to the Kunitz-type serine protease	inhibitors, including bovine pancreatic trypsin inhibit
Other	inhibitors involved in this process are noggin and chor
argely disappointing clinical results of MMP	inhibitors is unclear, especially in light of their act
The mechanism of DPP-4	inhibitors is to increase incretin levels (GLP-1 and GI
apy against bleeding; the incidence of these	inhibitors is dependent of various factors, including t
ACCase	Inhibitors kill grasses and inhibit the first step in l
ril was the first member of the group of ACE	inhibitors known as the dicarboxylate-containing ACE in
OPS online database for peptidases and their	inhibitors: LI27.001
ENTs are blocked by adenosine reuptake	inhibitors like dipyridamole and dilazep, drugs used cl
ge of ACE inhibition by active site-directed	inhibitors like captopril, enalapril, lisinopril, and o
nnels can still be inhibited by one of their	inhibitors, like Charybdotoxin (CTX)(Kaczorowski et al.
ACE	inhibitors like enalapril prevent this effect.
Dopamine β-hydroxylase (DBH)	inhibitors like disulfiram (Antabuse), which is used in
Tyrosine hydroxylase (TH)	inhibitors like metirosine (Demser), which is used in t
istration of Atorvastatin with one of CYP3A4	inhibitors like itraconazole, telithromycin and voricon
s is less likely to happen with other CYP3A4	inhibitors like diltiazem, erythromycin, fluconazole, k
might interact with dihydrofolate reductase	inhibitors like methotrexate and trimethoprim, and NO-e
OPS online database for peptidases and their	inhibitors: M10.006
OPS online database for peptidases and their	inhibitors: M10.009
OPS online database for peptidases and their	inhibitors: M10.013
OPS online database for peptidases and their	inhibitors: M10.014
OPS online database for peptidases and their	inhibitors: M10.017
OPS online database for peptidases and their	inhibitors: M10.019
OPS online database for peptidases and their	inhibitors: M10.051
OPS online database for peptidases and their	inhibitors: M12.021
OPS online database for peptidases and their	inhibitors: M12.208
OPS online database for peptidases and their	inhibitors: M12.220
OPS online database for peptidases and their	inhibitors: M12.222
OPS online database for peptidases and their	inhibitors: M12.235
OPS online database for peptidases and their	inhibitors: M18.002
dition of, or dosage change in, these CYP3A4	inhibitors makes it harder for the body to metabolize a
Exogenous angiogenesis	inhibitors may be drugs or a dietary components.
	Inhibitors may be present in the original sample, such
relevant to understanding how PDE5-selective	inhibitors may alter signal transduction pathways in ph
PDE5-selective	inhibitors may show good discrimination of PDE5 from mo
Because of the Akt[1] functions above Akt	inhibitors may treat cancers such as neuroblastoma.
mTOR	inhibitors may also be useful for treating several age-
OPS online database for peptidases and their	inhibitors: Metallo Peptidases
HIV protease	inhibitors, nefazodone, sertraline, grapefruit juice, f
tion of non-nucleoside reverse transcriptase	inhibitors, notably etravirine and rilpivirine.
ajor pharmaceutical companies are developing	inhibitors of the Na/glucose cotransporters to treat di
Tryptolines are also potent reuptake	inhibitors of serotonin and epinephrine, with a signifi
netrating peptides that act as intracellular	inhibitors of signal transference from receptors to G p
chemical compound, one of the noncompetitive	inhibitors of cytochrome P450 2C9.
breast cancer, a small-molecule or antibody	inhibitors of LOX abolished metastasis.
ine were synthesized that behave as combined	inhibitors of monoamine uptake and nAChRs.
(S)-thiorphan are isomeric thiol-containing	inhibitors of endopeptidase EC 24-11 (also called "enke
anticholinergics (benztropine), which act as	inhibitors of the neurotransmitter acetylcholine, may p
iopanoic acid and ipodate sodium are potent	inhibitors of thyroid hormone release from thyroid glan
role in drug-induced malformations is known:	inhibitors of the last step of cholesterol biosynthesis
Reversible	inhibitors of monoamine oxidase A (RIMAs) are a class o
Hydroxymates are particularly potent	inhibitors of MMPs and other zinc-dependent enzymes, du
gs didanosine and zidovudine are more potent	inhibitors of mitochondrial DNA synthesis than tenofovi
on and a related halogenated monoterpene are	inhibitors of the enzyme DNA methyltransferase, suggest
These include INKS for	inhibitors of kinase, KIPS for kinase inhibitors and CK
	Inhibitors of insect alpha-amylases from sorghum.
Many	inhibitors of glycosyltransferases are known.
d by a local balance between stimulators and	inhibitors of new vessel growth and is suppressed under
In 2005 it was shown that	inhibitors of EGFR could enhance axonal regeneration on
ed by a number of independent stimulators or	inhibitors of iron absorption.
Synthetic	inhibitors of the enzyme have been discovered.
The calphostins are	inhibitors of protein kinase C (PKC).
The Aminocoumarin antibiotics are known	inhibitors of DNA gyrase.

1 2 次へ＞

共起表現

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「INHIBITORS」の共起表現一覧(1語右で並び替え)