isoproterenol — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
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...		Endogenous Metabolite , Adrenergic Receptor
T25546	Isoproterenol tartrate, (-)-	L-Isoproterenol D-bitartrate,Isoproterenol D-bitartrate, L-,Isolevin
	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
	(S)-Isoproterenol bitartrate is a bioactive chemical.
T20122	Isoproterenol sulfate anhydrous	Norisodrine,Novodrine,Novodrin,dl-Isoproterenol sulfate,Isoprenaline sulphate,Aleudrin
	Isoproterenol sulfate anhydrous is a useful alkaloid. It is used for biological research.
T21411L	Isoproterenol bitartrate
	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...
T69598	Isoproterenol-d7 HCl
	Isoproterenol-d7 is intended for use as an internal standard for the quantification of isoproterenol by GC- or LC-MS. Isoproterenol is an agonist of β1- and β2-adrenergic receptors (β1- and β2-ARs; Kis = 224 and 458 nM, ...
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.		PI3K , Endogenous Metabolite , Adrenergic Receptor , PDE
T23312	SB 204741		5-HT Receptor
	SB 204741 is a 5-HT2B receptor antagonist.		5-HT Receptor
T69040	Dichloroisoproterenol
	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
	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...		Potassium Channel , Adrenergic Receptor
T3753	Sinapinic Acid	Sinapic acid,Synapoic acid	Apoptosis , RAAS , Reactive Oxygen Species , HDAC
	Sinapinic Acid (Synapoic acid) protects the rat liver from CCl4-induced inflammation, most likely by acting as a free radical scavenger and modulator of NF-κB p65 activation and proinflammatory cytokine expression. Sinap...		Apoptosis , RAAS , Reactive Oxygen Species , HDAC
T34329	Rimiterol
	Rimiterol, a beta 2 stimulant, therefore affects the cardiovascular system less than isoproterenol.
T70854	Protokylol hydrochloride
	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)
	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
	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
	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...
T71141	Fenspiride-d5
	Fenspiride-d5 is intended for use as an internal standard for the quantification of fenspiride by GC- or LC-MS. Fenspiride is an antagonist of histamine H1 receptors and a non-steroidal anti-inflammatory drug (NSAID). It...
T37475	Cyclic ADP-Ribose (ammonium salt)	cADP-Ribose,cADPR,Cyclic ADP-Ribose (ammonium salt)
	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
	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...