「adrenergic」の共起表現(1語右で並び替え)

「adrenergic」の共起表現一覧(1語右で並び替え)

adrenergic

1語右で並び替え

該当件数:83件

odafinil possesses greater selective alpha-1 adrenergic activity than adrafinil without the side eff
If the amine on the Adrenergic agent has a substituent bigger than a tertia
stituted phenethylamines are known to act as adrenergic agents (including adrenergic uptake inhibito
vity or idiosyncrasy to their components, to adrenergic agents or to other drugs of similar chemical
The pharmacologic effects of beta adrenergic agonist drugs, such as orciprenaline, are at
ptor agonist and also has some serotonin and adrenergic agonist effects, as well as some anticholine
Adrenergic agonists or withdrawal from alpha blockers (
It has the opposite effect as adrenergic agonists.
ine, and similarly to it, has effects on the adrenergic and dopaminergic systems.
ne and dopamine and therefore an increase in adrenergic and dopaminergic neurotransmission.
compensatory changes at dopamine, serotonin, adrenergic and histamine receptor sites in the central
An Adrenergic antagonist is a pharmaceutical substance tha
of beta-1 (ADRB1) may affect the response to adrenergic beta-antagonist treatment of heart failure.
cells), Ca2+ channel antagonistic action, α1 adrenergic blockade and others.
Guanadrel is a postganglionic adrenergic blocking agent.
Pirbuterol (trade name: Maxair) is a beta-2 adrenergic bronchodilator used in the treatment of asth
n primarily by increasing catecholaminergic ( adrenergic, dopaminergic) and histaminergic activity in
indicate that etilefrine has both β1 and α1 adrenergic effects in man.
ke inhibitor and has negligible affinity for adrenergic, histaminergic, and muscarinic receptors.
hypotension) which is followed by sustained adrenergic hyperactivity (hypertension, tachycardia, an
Adrenergic means "having to do with adrenaline (epineph
or a variety of dopaminergic, serotonergic, adrenergic, muscarinic or cannabinoid receptors and doe
ter release from sympathetic nerves and from adrenergic neurons in the central nervous system.
Effects on the body include cholinergic, adrenergic, opioid and nitric oxide donating actions, a
The adrenergic phase but not the cholinergic phase is a dos
Adrenergic receptor
The Adrenergic receptor Pathways
Adrenergic receptor agonist
Adrenergic receptor antagonist
Alpha-1 adrenergic receptor
It is a subtype of the adrenergic receptor family.
ICI-118,551 is a selective beta-2 (β2) adrenergic receptor antagonist.
Beta-3 adrenergic receptor has been shown to interact with Src
Beta adrenergic receptor kinase-2 appears to affect dopamine
ine is a nonselective agonist of the alpha-1 adrenergic receptor (α1-AR), and an antagonist to the a
The alpha-2A adrenergic receptor (α2A adrenoceptor), also known as A
Overall, the beta adrenergic receptor kinase 2 has 85% amino acid similar
Systemic Alpha-1 adrenergic receptor antagonists have been implicated in
(steps 1) Upon stimulation of the Beta adrenergic receptor by epinephrine, Gs will be activate
Beta adrenergic receptor kinase has been shown to interact w
is a cardiotonic drug which acts as a Beta-1 adrenergic receptor agonist.
The alpha-2B adrenergic receptor (α2B adrenoceptor), is a G-protein
The alpha-1 (α1) adrenergic receptor is a G protein-coupled receptor (GP
Beta adrenergic receptor kinase (also referred to as βARK or
It acts as both a selective α2 adrenergic receptor antagonist, and an antagonist for t
ent and selective antagonist for the Alpha-1 adrenergic receptor subtype α1B.
Adrenergic receptor antagonist, subtypes α2a and α2c: c
The beta adrenergic receptor kinase-2 was cloned from mice and r
It is an alpha-1 adrenergic receptor blocker that inhibits the binding o
, did not find that the gene coding for beta adrenergic receptor kinase-2 was linked to schizophreni
he NMDA antagonist tiletamine or the alpha-2 adrenergic receptor agonist xylazine, depending on what
a2A-adrenoceptor (also known as the alpha-2A adrenergic receptor) has been shown to improve working
t acts as a selective antagonist for the α2B adrenergic receptor, and has been useful for distinguis
research to understand the action of the β2 adrenergic receptor, as few other specific antagonists
, GAB1, MST1R, DNM1, Huntingtin, Src, Beta-2 adrenergic receptor, VAV2, ADAM15, RAPGEF1, VAV1, HER2/
onidine, it is an agonist at the α2 class of adrenergic receptor.
which acts as a selective agonist for the β3 adrenergic receptor.
nist at both the 5-HT1A receptor and the α2C adrenergic receptor.
which acts as a selective agonist for the β3 adrenergic receptor.
of drugs that bind selectively to the beta-1 adrenergic receptor.
2 dopamine receptor and antagonist at the α1 adrenergic receptor.
fect on heart muscle, when binding to beta-1 adrenergic receptors on this tissue.
Beta adrenergic receptors are involved in the epinephrine- a
regulated by norepinephrine (noradrenaline) ( adrenergic receptors), whereas parasympathetic systems
thylclonidine is an irreversible agonist for adrenergic receptors, in particular alpha1B, D, C and a
ated via a partial agonist action at Alpha-2 adrenergic receptors, and TDIQ has been suggested as a
y blocking a variety of receptors, including adrenergic receptors, dopamine receptors, histamine rec
It stimulates adrenergic receptors.
It has no effect on alpha or beta adrenergic receptors.
nzamine forms a permanent covalent bond with adrenergic receptors.
metic that nonselectively agonizes α1 and α2 adrenergic receptors.
t also interacts centrally with dopamine and adrenergic receptors.
upling in the rat parotid gland and at alpha adrenergic receptors.
tivated through protein receptors such as α1 adrenergic receptors.
hilic side-chain that binds to an exosite on adrenergic receptors.
oson vasodilates but does not stimulate beta adrenergic receptors.
mals, suggesting stimulation of both α and β adrenergic receptors.
de, where they can come into contact with β2 adrenergic receptors.
Adrenergic reuptake inhibitor
and thereby rendering it less responsive to adrenergic stimulation ).
ppear to be mediated by the dopaminergic and adrenergic systems.
It localizes to adrenergic tissue and thus can be used to identify the
Adrenergic transporter