Glycine is a non-chiral amino acid that can be synthesized in the body from the amino acid serine by Serine Hydroxymethyltransferase. Acts as an inhibitory neurotransmitter Shown to block NMDA-stimulated dopamine release in fetal mesencephalic cell
Glycine is a non-chiral amino acid that can be synthesized in the body from the amino acid serine by Serine Hydroxymethyltransferase. Acts as an inhibitory neurotransmitter Shown to block NMDA-stimulated dopamine release in fetal mesencephalic cell
Poly-lysine is a polycation which binds to DNA, red cell membrane and any negatively charged protein. Molecular weight has been determined by Viscosity as well as by HPLC.
Poly-lysine is a polycation which binds to DNA, red cell membrane and any negatively charged protein. Molecular weight has been determined by Viscosity as well as by HPLC.
(±)-Verapamil Hydrochloride is a &alpha1-antagonist and calcium channel modulator. (±)-Verapamil hydrochloride is a calcium channel (L-type) modulator, adrenoceptor antagonist, anti-arrhythmic, cardiac depressant, and coronary
(±)-Verapamil Hydrochloride is a &alpha1-antagonist and calcium channel modulator. (±)-Verapamil hydrochloride is a calcium channel (L-type) modulator, adrenoceptor antagonist, anti-arrhythmic, cardiac depressant, and coronary
(±)-Verapamil Hydrochloride is a &alpha1-antagonist and calcium channel modulator. (±)-Verapamil hydrochloride is a calcium channel (L-type) modulator, adrenoceptor antagonist, anti-arrhythmic, cardiac depressant, and coronary
(±)-Verapamil Hydrochloride is a &alpha1-antagonist and calcium channel modulator. (±)-Verapamil hydrochloride is a calcium channel (L-type) modulator, adrenoceptor antagonist, anti-arrhythmic, cardiac depressant, and coronary
Norethindrone is a synthetic progestin that possesses antiestrogenic effects, where in low doses it is progestational and in high doses it is antiestrogenic. It also causes a time-dependent loss of cytochrome P-450 when incubated in vitro with rat
Norethindrone is a synthetic progestin that possesses antiestrogenic effects, where in low doses it is progestational and in high doses it is antiestrogenic. It also causes a time-dependent loss of cytochrome P-450 when incubated in vitro with rat
Hydroxyurea is a inhibitor of DNA synthesis in vivo, and an antiviral and antineoplastic agent which is S-phase specific. A ribonucleotide reductase inhibitor - inhibits by forming a free radical nitroxide that binds a tyrosyl free radical in the
Hydroxyurea is a inhibitor of DNA synthesis in vivo, and an antiviral and antineoplastic agent which is S-phase specific. A ribonucleotide reductase inhibitor - inhibits by forming a free radical nitroxide that binds a tyrosyl free radical in the
Eosin Y, a red xanthene dye, has been noted to reduce the affinity of Mg2+- ATPase for ATP and increase the enzyme affinity for Mg2+ at concentrations of 10-50 &muM. At higher concentrations near 100 &muM the affinity for Mg2+- ATPase for the
Eosin Y, a red xanthene dye, has been noted to reduce the affinity of Mg2+- ATPase for ATP and increase the enzyme affinity for Mg2+ at concentrations of 10-50 &muM. At higher concentrations near 100 &muM the affinity for Mg2+- ATPase for the
Adenosine is a nucleotide resulting from the union of one molecule of sugar -- d-ribose -- with a base -- l-adenine. Active in cardiovascular disorders Indicated in cases of angina pectoris Increases coronary output Vasodilator action Induced
Adenosine is a nucleotide resulting from the union of one molecule of sugar -- d-ribose -- with a base -- l-adenine. Active in cardiovascular disorders Indicated in cases of angina pectoris Increases coronary output Vasodilator action Induced