![]() DL-ALPHA-(METHYLAMINOMETHYL)BENZYL ALCOHOL structure
|
Common Name | DL-ALPHA-(METHYLAMINOMETHYL)BENZYL ALCOHOL | ||
---|---|---|---|---|
CAS Number | 6589-55-5 | Molecular Weight | 151.206 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 244.1±7.0 °C at 760 mmHg | |
Molecular Formula | C9H13NO | Melting Point | 74-76ºC | |
MSDS | Chinese USA | Flash Point | 96.3±8.7 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
MMA/MPEOMA/VSA copolymer as a novel blood-compatible material: ex vivo platelet adhesion study.
J. Mater. Sci. Mater. Med. 15(2) , 155-9, (2004) MMA/MPEOMA/VSA copolymers with both pendant polyethylene oxide (PEO) side chains and negatively chargeable side groups were synthesized by random copolymerization of methyl methacrylate (MMA), methoxy PEO monomethacrylate (MPEOMA; PEO mol. wt, 1000), and viny... |
|
Phe310 in transmembrane VI of the alpha1B-adrenergic receptor is a key switch residue involved in activation and catecholamine ring aromatic bonding.
J. Biol. Chem. 274(23) , 16320-30, (1999) Pharmacophore mapping of adrenergic receptors indicates that the phenyl ring of catecholamine agonists is involved in receptor binding and activation. Here we evaluated Phe310, Phe311, and Phe303 in transmembrane VI (TMVI), as well as Tyr348 in TMVII of the a... |
|
Characterization of N-methylphenylethylamine and N-methylphenylethanolamine as substrates for type A and type B monoamine oxidase.
Biochem. Pharmacol. 29(19) , 2663-7, (1980)
|
|
Elimination of ephedrines in urine following multiple dosing: the consequences for athletes, in relation to doping control.
Br. J. Clin. Pharmacol. 57(1) , 62-7, (2004) To study the elimination of ephedrines with reference to the International Olympic Committee (IOC) doping control cut-off levels, following multiple dosing of over-the-counter decongestant preparations.A double-blind study was performed in which 16 healthy ma... |
|
Two general routes to 1,4-disubstituted-2,3,4,5-tetrahydro- 1H-3-benzazepines.
Org. Lett. 2(25) , 4099-102, (2000) [structure] Two general routes to 1,4-disubstituted-2,3,4, 5-tetrahydro-1H-3-benzazepines are described. Both routes utilize an appropriately functionalized phenethylamino alcohol as the penultimate intermediate: the first route makes use of the reductive ami... |
|
The vasoactive potential of halostachine, an alkaloid of tall fescue (Festuca arundinaceae, Schreb) in cattle.
Vet. Hum. Toxicol. 25(6) , 408-11, (1983)
|
|
Physiologic effects and plasma kinetics of phenylethanolamine and its N-methyl homolog in the dog.
J. Pharmacol. Exp. Ther. 217(2) , 379-85, (1981) Single i.v. doses of the endogenous trace amine phenylethanolamine (PEOH) and its N-methyl homolog (NMPEOH) were administered to separate groups of five dogs. The dose- and time-related effects of these compounds were measured on pupillary diameter, heart rat... |
|
A new method for in vivo measurement of brain monoamine oxidase activity.
Prog. Neuropsychopharmacol. Biol. Psychiatry 8(3) , 385-95, (1984) The radiotracers, C-14-N-methylphenylethylamine (MPEA) and N-methylphenylethanolamine (MPEOA) both rapidly entered mouse brain after their intravenous injection and were metabolized by brain monoamine oxidase (MAO) to C-14-methylamine and corresponding aldehy... |