|
T21411 |
Isoproterenol
|
Norisodrine,Isoprenaline,Novodrin,Isuprel,Medihaler-Iso |
Endogenous Metabolite
,
Adrenergic Receptor
|
|
Isoproterenol (Norisodrine) is a non-selective and orally active β-adrenoceptor agonist.Isoproterenol is a potent peripheral vasodilator and bronchodilator.Isoproterenol can be used in the study of bradycardia and bronch... |
|
T25546 |
Isoproterenol tartrate, (-)-
|
L-Isoproterenol D-bitartrate,Isoproterenol D-bitartrate, L-,Isolevin |
Others
|
|
Isoproterenol tartrate, (-)- is a beta-Adrenoceptor agonist agent that increases cytosolic cAMP. |
|
T29262 |
(S)-Isoproterenol bitartrate
|
EINECS 238-683-4,d-Isoproterenol bitartrate,L-(+)-Isoproterenol bitartrate,d-N-Isopropylnorepinephrine bitartrate |
Others
|
|
(S)-Isoproterenol bitartrate is a bioactive chemical. |
|
T20122 |
Isoproterenol sulfate anhydrous
|
Norisodrine,Novodrine,Novodrin,dl-Isoproterenol sulfate,Isoprenaline sulphate,Aleudrin |
Others
|
|
Isoproterenol sulfate anhydrous is a useful alkaloid. It is used for biological research. |
|
T21411L |
Isoproterenol bitartrate
|
|
Others
|
|
Isoproterenol bitartrate is a beta-sympathomimetic and an isopropyl analog of Epinephrine, which acts on the heart, bronchi, skeletal muscle, and alimentary tract. It is used mainly as a bronchodilator and heart stimulan... |
|
T1056 |
Isoprenaline hydrochloride
|
NCI-c55630,Isoproterenol hydrochloride,Isoprenaline HCl |
PI3K
,
Endogenous Metabolite
,
Adrenergic Receptor
,
PDE
|
|
Isoprenaline hydrochloride (NCI-c55630) is a potent beta-adrenergic agonist with the peripheral vasodilator, bronchodilator, and cardiac stimulating properties. |
|
T84859 |
(-)-Isoproterenol hydrochloride
|
|
Others
|
|
(-)-Isoproterenol hydrochloride is used as a β-adrenergic receptor agonist in the treatment of bradycardia and as a bronchodilator. |
|
T23312 |
SB 204741
|
|
5-HT Receptor
|
|
SB 204741 is a selective 5-HT2B antagonist with high affinity and pKi value of 7.1. |
|
T69040 |
Dichloroisoproterenol
|
|
Others
|
|
Dichloroisoproterenol is also known as Dichloroisoprenaline (DCI), was the first beta blocker ever to be developed. It is non-selective for the β1-adrenergic and β2-adrenergic receptors. DCI has low potency and acts as a... |
|
T31435 |
Dichloroisoproterenol hydrochloride
|
DCI hydrochloride,Dichloroisoprenaline hydrochloride,Dichloroisoproterenol HCl |
Others
|
|
Dichloroisoproterenol hydrochloride is a biochemical. It may be used for cardiac arrhythmia. |
|
T26822 |
Bisaramil hydrochloride
|
RGH-2957,NK 1556,NK1556,Bisaramil,NK-1556,RGH 2957 |
Potassium Channel
,
Adrenergic Receptor
|
|
Bisaramil hydrochloride (Bisaramil) is a novel diazabicyclononane antiarrhythmic compound that inhibits the generation of free radicals.Bisaramil hydrochloride blocks sodium currents and inhibits the slow Ca(2+) action p... |
|
T34329 |
Rimiterol
|
|
Others
|
|
Rimiterol, a beta 2 stimulant, therefore affects the cardiovascular system less than isoproterenol. |
|
T70854 |
Protokylol hydrochloride
|
|
Others
|
|
Protokylol hydrochloride is the salt form of Protokylol (free base) (Asmetil, Caytine, Palison, Ventaire), a β-adrenergic receptor agonist used as a bronchodilator in Europe and the United States. It is methylenedioxyphe... |
|
T69126 |
Clofeverine (free base)
|
|
Others
|
|
Clofeverine (free base) is a highly selective relaxant for gastrointestinal smooth muscles with a beta-receptor stimulative nature. On isolated ileum, the inhibitory effect of clofeverine for spontaneous motility was com... |
|
T69324 |
Clofeverine hydrochloride
|
|
Others
|
|
Clofeverine hydrochloride is the salt form of Clofeverine (free base), a highly selective relaxant for gastrointestinal smooth muscles with a beta-receptor stimulative nature. On isolated ileum, the inhibitory effect of ... |
|
T37896 |
AZ 1729
|
|
Others
|
|
FFA2 allosteric agonist. Inhibits forskolin-induced cAMP increase and stimulates 35SGTPγS binding in biochemical assays (pEC50 values are 6.9 and 7.23, respectively). Binds at allosteric binding site. In functional assay... |
|
T37475 |
Cyclic ADP-Ribose (ammonium salt)
|
cADP-Ribose,cADPR,Cyclic ADP-Ribose (ammonium salt) |
Others
|
|
Cyclic ADP-ribose (cADP-ribose) is an endogenous metabolite of NAD+ that mobilizes the release of stored Ca2+ in the endoplasmic reticulum via ryanodine receptors in various cell types.[1],[2],[3],[4],[5] This second mes... |
|
T36679 |
Rp-cAMPS sodium salt
|
|
Others
|
|
Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis b... |
