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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
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. | |||
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... | |||
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 |
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)... | |||
T68242 | D-Mabuterol hydrochloride | ||
D-Mabuterol hydrochloride is a selective β2 adrenoreceptor agonist. Mabuterol inhibited the positive inotropic effect of isoprenaline. | |||
T69084 | Mabuterol, (R)- | ||
Mabuterol, (R)- is a selective β2 adrenoreceptor agonist. Mabuterol inhibited the positive inotropic effect of isoprenaline. | |||
T69085 | Mabuterol, (S)- | ||
Mabuterol, (S)- is a selective β2 adrenoreceptor agonist. Mabuterol inhibited the positive inotropic effect of isoprenaline. | |||
T60713 | TK-129 | ||
TK-129 is an orally active, potent inhibitor of KDM5B with IC 50 of 44 nM that is low-toxicity. TK-129 shows cardioprotective effects by inhibiting KDM5B and blocking the KDM5B -associated Wnt pathway. TK-129 can be used... |