phenylephrine — TargetMol Chemicals

Cat No.	Product Name	Synonyms	Targets
T17310	Phenylephrine	L-Phenylephrine,(R)-(-)-Phenylephrine	Adrenergic Receptor
	Phenylephrine ((R)-(-)-Phenylephrine) is a selective α1-adrenoceptor agonist ( pKi: 5.86, 4.87 and 4.70 for α1D, α1B, and α1A receptors respectively).		Adrenergic Receptor
T0453	Phenylephrine hydrochloride	NCI-c55641,Phenylephrine HCl,(R)-(-)-Phenylephrine hydrochloride	Endogenous Metabolite , Adrenergic Receptor
	Phenylephrine hydrochloride (NCI-c55641) is a selective agonist of the α1-adrenergic receptor.		Endogenous Metabolite , Adrenergic Receptor
T0453L	DL-Phenylephrine HCl	Eyelo,DL-Phenylephrine hydrochloride
	DL-Phenylephrine HCl is a selective agonist of the alpha1-adrenergic receptor.
T35576	Phenylephrine-3-O-Sulfate
	Phenylephrine-3-O-sulfate is metabolite of the α1A-adrenergic receptor agonist phenylephrine formed via sulfation.
T68997	L-Phenylephrine
	L-Phenylephrine is an alpha-adrenergic agonist used as a mydriatic, nasal decongestant, and cardiotonic agent.
T22033	ARC 239 dihydrochloride		Norepinephrine
	ARC 239 dihydrochloride is a selective α2B adrenoceptor antagonist (pKD values are 8.8, 6.7 and 6.4 at α2B, α2A, and α2D receptors respectively).		Norepinephrine
T7634	3-Hydroxymandelic Acid		Endogenous Metabolite
	3-Hydroxymandelic Acid is a metabolite of Phenylephrine.		Endogenous Metabolite
T5263	P-Hydroxymandelic acid	4-Hydroxymandelic acid	Others , Endogenous Metabolite
	p-Hydroxymandelic acid (4-Hydroxymandelic acid) is an acidic metabolite of p-octopamine and p-synephrine (p-phenylephrine). It is also a naturally occurring metabolite of tyramine.		Others , Endogenous Metabolite
T2944	Danshensu sodium salt	Sodium Danshensu,(±)-DanShenSu sodium salt,(±)-DanShenSu sodium sal	P450 , Autophagy
	Danshensu sodium salt (Sodium Danshensu) is sodium salt of danshensu from the widely used Chinese herb Danshen. It can inhibited phenylephrine- and CaCl2-induced vasoconstriction in Ca2+-free medium.		P450 , Autophagy
T4563	Thonzylamine	neohetramine	Histamine Receptor
	Thonzylamine (neohetramine) is an antihistamine and anticholinergic drug. It is available as combination products with Clofedanol or Phenylephrine for temporary relief of symptoms of common cold, hay fever (allergic rhin...		Histamine Receptor
TN1624	Ethyl cinnamate		Calcium Channel , ROS , NO Synthase
	Ethyl cinnamate has antifungal, and vasorelaxant effects. Ethyl cinnamate can lead to the damage of cell membrane system and metabolic disorder through inducing lipid peroxidation via initiating ROS overproduction. Ethyl...		Calcium Channel , ROS , NO Synthase
T12913	Siguazodan	SKF 94836	PDE
	Siguazodan (SKF 94836) is an effective, selective, orally active phosphodiesterase III ((PDE-III)) inhibitor with an IC50 of 117 nM. Siguazodan inhibited phenylephrine induced 5-HT release with an IC50 value of 4.2 μM。 S...		PDE
T23557	Talibegron hydrochloride	ZD2079 hydrochloride,ZD 2079	Adrenergic Receptor
	Talibegron hydrochloride (ZD2079 hydrochloride) is an β3 adrenergic receptor agonist with a pD2 of 3.72 on phenylephrine-preconstricted rat mesenteric artery. Relaxes rat mesenteric artery and isolated aorta in vitro. In...		Adrenergic Receptor
TN1724	Harmalol hydrochloride	Harmidol hydrochloride	P450 , Antioxidant
	Harmalol hydrochloride (Harmidol hydrochloride) is a β-carboline alkaloid that can be extracted from the seeds of Peganum harmala L. Harmalol hydrochloride is the major metabolite of Harmaline and significantly inhibits ...		P450 , Antioxidant
T30427	Berefrine
	Berefrine is an Oxazolidine prodrug of phenylephrine.
T40563	Sandaracopimaric acid
	Sandaracopimaric acid is an anti-inflammatory diterpenoid compound that effectively reduces the contraction of phenylephrine-induced pulmonary arteries. With an EC50 of 43.93 μM, it exhibits noteworthy anti-inflammatory ...
T27164	DHP-218	PAK-9,PAK9,PAK 9,DHP218
	DHP-218 is a calcium channel antagonist. DHP-218 inhibits Calcium-induced contraction of the rat aorta in high K+ solution with the pA2 value of 9.11. The IC50 value for the inhibitory effects of DHP-218 in high K+-induc...
T73083	Nipradolol	KT 210 ; K 351 ; Hypadil,Hypadil,KT 210,K 351
	Nipradolol (KT-210; K-351), an alpha-1-adrenergic receptor antagonist, effectively inhibits the elevation of intraocular pressure (IOP) induced by Phenylephrine in an albino rabbit model and suppresses noradrenaline (NA)...
TP2086	AdTx1
	Selective, high affinity, non-competitive α1A adrenoceptor antagonist (Ki = 0.35 nM). Exhibits no significant activity against a range of other GPCRs, including α2A, β1 and β2 adrenoceptors. Antagonizes effects of phenyl...
T39281	AM404
	AM404 is a chemical compound that functions as an inhibitor of endocannabinoid reuptake. It effectively blocks the transport of anandamide, with IC50 values measured in the low micromolar range. Moreover, AM404 exhibits ...