DOPA
Brand names,
DOPA
Analogs
DOPA
Brand Names Mixture
DOPA
Chemical_Formula
C8H11NO2
DOPA
RX_link
http://www.rxlist.com/cgi/generic3/dopamine.htm
DOPA
fda sheet
DOPA
msds (material safety sheet)
DOPA
Synthesis Reference
No information avaliable
DOPA
Molecular Weight
153.178 g/mol
DOPA
Melting Point
82.5 oC
DOPA
H2O Solubility
600 g/L
DOPA
State
Solid
DOPA
LogP
0.548
DOPA
Dosage Forms
Solution
DOPA
Indication
For the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery, renal failure, and chronic cardiac decompensation as in congestive failure
DOPA
Pharmacology
Dopamine is a natural catecholamine formed by the decarboxylation of 3,4-dihydroxyphenylalanine (DOPA). It is a precursor to norepinephrine in noradrenergic nerves and is also a neurotransmitter in certain areas of the central nervous system, especially in the nigrostriatal tract, and in a few peripheral sympathetic nerves. Dopamine produces positive chronotropic and inotropic effects on the myocardium, resulting in increased heart rate and cardiac contractility. This is accomplished directly by exerting an agonist action on beta-adrenoceptors and indirectly by causing release of norepinephrine from storage sites in sympathetic nerve endings.
DOPA
Absorption
Dopamine is rapidly absorbed from the small intestine.
DOPA
side effects and Toxicity
LD50 oral mice = 1460 mg/kg, LD50 oral rats = 1780 mg/kg. Spasm or closing of eyelids, nausea, vomiting, cardiac arrhythmias, involuntary movements of the body including the face, tongue, arms, hand, head, and upper body; hypotension, haemolytic anaemia, urinary retention, duodenal ulcer, sialorrhea, ataxia, abdominal pain, dry mouth, nightmares, tachypnoea, bruxism, confusion, and insomnia.
DOPA
Patient Information
No information avaliable
DOPA
Organisms Affected
Humans and other mammals