Chlortalidone or chlorthalidone

Biochem/physiol Actions Phentermine is a sympathomimetic that releases norepinephrine and epinephrine in CNS and periphery reducing hunger. Similarly to other amphetamines, phentermine potently inhibits DA and 5-HT uptake.

Biochem/physiol Actions Lurasidone is an atypical antipsychotic, used clinically for treatment of schizophrenia and bi-polar disorder. It has nanomolar activity as an antagonist at dopamine D2, serotonin 5-HT2A, 5-HT7, and &#945:2C-adrenergic

Biochem/physiol Actions Lurasidone is an atypical antipsychotic, used clinically for treatment of schizophrenia and bi-polar disorder. It has nanomolar activity as an antagonist at dopamine D2, serotonin 5-HT2A, 5-HT7, and &#945:2C-adrenergic

Biochem/physiol Actions R-568 is a positive allosteric modulator of the calcium-sensing receptor (CaSR), increasing the sensitivity to activation by extracellular Ca 2+ . In rats, orally administered R-568 decreases plasma levels of PTH and Ca 2+

Biochem/physiol Actions R-568 is a positive allosteric modulator of the calcium-sensing receptor (CaSR), increasing the sensitivity to activation by extracellular Ca 2+ . In rats, orally administered R-568 decreases plasma levels of PTH and Ca 2+

Biochem/physiol Actions Phevamine A is a bacterial ( Pseudomonas syringae , Erwinia amylovora , …) virulence factor that promotes phytopathogens growth by suppression of host immune response in both A. thaliana and Nicotiana bentha

Biochem/physiol Actions Phevamine A is a bacterial ( Pseudomonas syringae , Erwinia amylovora , …) virulence factor that promotes phytopathogens growth by suppression of host immune response in both A. thaliana and Nicotiana bentha

Biochem/physiol Actions Ziprasidone is an atypical antipsychotic with 5HT1A agonist, as well as D2, 5HT2A, and 5HT1D antagonist activity.

Biochem/physiol Actions Ziprasidone is an atypical antipsychotic with 5HT1A agonist, as well as D2, 5HT2A, and 5HT1D antagonist activity.

Biochem/physiol Actions SG-005, a tetrandrine derivative, is a potent and selective inhibitor of two-pore channel 2 (TPC2) that exhibits antiproliferative properties against cancer cells.

Biochem/physiol Actions SG-005, a tetrandrine derivative, is a potent and selective inhibitor of two-pore channel 2 (TPC2) that exhibits antiproliferative properties against cancer cells.

General description This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the