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Cat. No.	Product Name	Target	Signaling Pathways
T1056	Isoprenaline hydrochloride NCI-c55630,Isoproterenol hydrochloride,Isoprenaline HCl,盐酸异丙肾上腺素	PI3K; Endogenous Metabolite; Adrenergic Receptor; PDE	GPCR/G Protein; Metabolism; Neuroscience; PI3K/Akt/mTOR signaling
	Isoprenaline hydrochloride (NCI-c55630) 是非选择性的β-肾上腺素能受体激动剂，有支气管扩张剂，外周血管扩张剂和心脏刺激活性。
T21411	Isoproterenol Norisodrine,Isoprenaline,Novodrin,Isuprel,Medihaler-Iso	Endogenous Metabolite; Adrenergic Receptor	GPCR/G Protein; Metabolism; Neuroscience
	Isoproterenol (Norisodrine) 是一种非选择性且具有口服活性的 β-肾上腺素受体激动剂。Isoproterenol 是有效的外周血管扩张剂和支气管扩张剂。Isoproterenol 可用于研究心动过缓和支气管哮喘，用于治疗心脏传导阻滞、心动过缓。
T32697	Levisoprenaline (R)-Isoprenaline,Levisoprenalina,BRN-3203136,BRN 3203136,Proternol L
	Levisoprenaline 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.
T68259	TUPS
	TUPS is a selective soluble epoxide hydrolase inhibitor which protects against isoprenaline-induced cardiac hypertrophy.
T27970	Mabuterol free base Mabuterol,PB 868Cl	Others	Others
	Mabuterol is a selective agonist of β2 adrenoreceptor with no beta 1-stimulation. Mabuterol inhibited the positive inotropic effect of isoprenaline at 10(-7) g/ml and decreased the maximum driving frequency at 3 X 10(-6) g/ml. Mabuterol was 3 times more p
T69085	Mabuterol, (S)-
	Mabuterol, (S)- is a D isoform of Mabuterol, which is a selective β2 adrenoreceptor agonist. Mabuterol has been found to decrease the blood pressure in rats and increase heart rate and contractile force in guinea pigs. Mabuterol inhibited the positive inotropic effect of isoprenaline but has no effect on alpha-adrenergic, acetylcholine and histamine receptors.
T68242	D-Mabuterol hydrochloride
	D-Mabuterol hydrochloride is a D isoform of Mabuterol, which is a selective β2 adrenoreceptor agonist. Mabuterol has been found to decrease the blood pressure in rats and increase heart rate and contractile force in guinea pigs. Mabuterol inhibited the positive inotropic effect of isoprenaline but has no effect on alpha-adrenergic, acetylcholine and histamine receptors.
T69084	Mabuterol, (R)-
	Mabuterol, (R)- is a D isoform of Mabuterol, which is a selective β2 adrenoreceptor agonist. Mabuterol has been found to decrease the blood pressure in rats and increase heart rate and contractile force in guinea pigs. Mabuterol inhibited the positive inotropic effect of isoprenaline but has no effect on alpha-adrenergic, acetylcholine and histamine receptors.
T60713	TK-129
	TK-129 是具有口服活性的 KDM5B 的有效抑制剂，IC50值为44 nM，并且具有低毒性。TK-129 发挥心脏保护作用，通过抑制 KDM5B 和阻断 KDM5B 相关的 Wnt 通路。TK-129 可用于研究心血管疾病，它能在体内减少异丙肾上腺素诱导的心肌重塑和纤维化，并且在体外减少 Ang II 诱导的心脏成纤维细胞活化。