Domperidone

3-Hydroxy-1,2-dimethyl-4(1 H )-pyridone (Hdpp, Deferiprone) is a hydroxy ketone derivative. It reacts with uranyl salts [UO 2 (NO 3 ) 2 ] in aqueous acidic solution to afford mono nuclear complexes ([UO 2 (dpp)(Hdpp) 2 (H 2 O)]ClO 4 ).

3-Hydroxy-1,2-dimethyl-4(1 H )-pyridone (Hdpp, Deferiprone) is a hydroxy ketone derivative. It reacts with uranyl salts [UO 2 (NO 3 ) 2 ] in aqueous acidic solution to afford mono nuclear complexes ([UO 2 (dpp)(Hdpp) 2 (H 2 O)]ClO 4 ).

A Snap-N-Spike &#174 Reference Solution suitable to use in LC/MS or GC/MS applications for urine drug testing, clinical toxicology, and forensic analysis. Also known as paliperidone, 9-Hydroxyrisperidone is sold under the brand name Invega, an

An internal standard suitable for use in LC/MS or GC/MS applications including forensic analysis, clinical toxicology, urine drug testing, or isotope dilution methods. Also known as paliperidone, 9-Hydroxyrisperidone is sold under the brand name

Biochem/physiol Actions Chromeceptin inhibits Insulin-like growth factor 2 (IGF2) signaling by a process that begins with chromeceptin binding to multifunctional protein 2 (MFP-2). This interaction stimulates the expression of IGF binding protein 1

Biochem/physiol Actions Peripheral dopamine receptor antagonist that does not cross the blood-brain barrier anti-emetic. Features and Benefits This compound was developed by Johnson &amp Johnson .

Biochem/physiol Actions Peripheral dopamine receptor antagonist that does not cross the blood-brain barrier anti-emetic. Features and Benefits This compound was developed by Johnson &amp Johnson .

Biochem/physiol Actions Peripheral dopamine receptor antagonist that does not cross the blood-brain barrier anti-emetic. Features and Benefits This compound was developed by Johnson &amp Johnson .

A cell-permeable, neutrally charged, pyridinium-to-pyridine substituted YM-01 (Cat. No.

A cell-permeable rhodacyanine derivative that stabilizes Hsp70 (heat-shock protein 70) in its ADP-bound, substrate-binding conformation via reversible binding to Hsp70 nucleotide-binding domain ( K D = 4.9 &#181M using YM-1-biotin) in a manner

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