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Hexestrol 200mg  | Purity Not Available

Selleck Chemicals

Hexestrol (Bibenzyl) binds to ERα and ERβ with EC50 of 0.07 nM and 0.175 nM, respectively.

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Imatinib 250mg  | Purity Not Available

Selleck Chemicals

Imatinib is a multi-target inhibitor of tyrosine kinase with inhibition for v-Abl, c-Kit and PDGFR, IC50 values are 0.6 μM, 0.1 μM and 0.1 μM in cell-free or cell-based assays, respectively. Imatinib (STI571) induces autophagy.

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Bupivacaine HCl 50mg  | Purity Not Available

Selleck Chemicals

Bupivacaine HCl binds to the intracellular portion of voltage-gated sodium channels and blocks sodium influx into nerve cells, used for treating cardiac arrhythmias.

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Bupivacaine HCl 10mM/1mL  | Purity Not Available

Selleck Chemicals

Bupivacaine HCl binds to the intracellular portion of voltage-gated sodium channels and blocks sodium influx into nerve cells, used for treating cardiac arrhythmias.

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Bethanechol chloride 50mg  | Purity Not Available

Selleck Chemicals

Bethanechol chloride(Myocholine,Urecholine) is a selective muscarinic receptor agonist without any effect on nicotinic receptors.

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Chlorpromazine HCl 50mg  | Purity Not Available

Selleck Chemicals

Chlorpromazine HCl is a dopamine and potassium channel inhibitor with IC50 of 6.1 and 16 μM for inward-rectifying K+ currents and time-independent outward currents.

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Chlorpromazine HCl 10mM/1mL  | Purity Not Available

Selleck Chemicals

Chlorpromazine HCl is a dopamine and potassium channel inhibitor with IC50 of 6.1 and 16 μM for inward-rectifying K+ currents and time-independent outward currents.

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Clindamycin HCl 50mg  | Purity Not Available

Selleck Chemicals

Clindamycin HCl inhibits protein synthesis by acting on the 50S ribosomal, used for the treatment of bacterial infections.

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Clonidine HCl 50mg  | Purity Not Available

Selleck Chemicals

Clonidine HCl(Kapvay) is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg.

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Pramipexole 20mg  | Purity Not Available

Selleck Chemicals

Pramipexole (SND 919,Mirapexin,Sifrol,Mirapex) is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively.

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