Cimaterol 25mg 25mg | Purity Not Available
Adooq Bioscience
Cimaterol is a potent agonist of β-adrenergic receptors (pEC50 = 8.13, 8.78, and 6.62 for human β1, β2, and β3, respectively).
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Cimaterol 10mg 10mg | Purity Not Available
Adooq Bioscience
Cimaterol is a potent agonist of β-adrenergic receptors (pEC50 = 8.13, 8.78, and 6.62 for human β1, β2, and β3, respectively).
More Information Supplier PageBupranolol 500mg 500mg | Purity Not Available
Adooq Bioscience
Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity.
More Information Supplier PageBupranolol 200mg 200mg | Purity Not Available
Adooq Bioscience
Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity.
More Information Supplier PageBupranolol 100mg 100mg | Purity Not Available
Adooq Bioscience
Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity.
More Information Supplier PageBRL 44408 maleate 50mg 50mg | Purity Not Available
Adooq Bioscience
BRL 44408 maleate is a high purity Adrenoceptors antagonist. It increases hippocampal noradrenalin release following systemic administration.
More Information Supplier PageBRL 44408 maleate 25mg 25mg | Purity Not Available
Adooq Bioscience
BRL 44408 maleate is a high purity Adrenoceptors antagonist. It increases hippocampal noradrenalin release following systemic administration.
More Information Supplier PageBRL 44408 maleate 10mg 10mg | Purity Not Available
Adooq Bioscience
BRL 44408 maleate is a high purity Adrenoceptors antagonist. It increases hippocampal noradrenalin release following systemic administration.
More Information Supplier PageBopindolol malonate 500mg 500mg | Purity Not Available
Adooq Bioscience
BCH 250mg 250mg | Purity Not Available
Adooq Bioscience
BCH is an inhibitor of L-type amino acid transporter LAT1. Suppresses growth and induces apoptosis via activation of caspases in KB, Saos2 and C6 cancer cell lines.
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