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m-30 dihydrochloride

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  • Inhibitors & Agonists
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MAO-IN-M30 dihydrochloride
M 30 dihydrochloride
T3803464821-19-8
MAO-IN-M30 dihydrochloride (M 30 dihydrochloride) is a potent and brain selective monoamine oxidase (MAO) inhibitor (EC50 values are 37 and 57 nM for MAO-A and MAO-B, respectively). Also an iron chelator with antioxidant properties. Protects cells against 6-OHDA induced apoptosis. Attenuates MPTP depletion of DA and increases striatal monoamine levels in a mouse Parkinson's disease model.
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6-8 weeks
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CRT0066101 dihydrochloride(956121-30-5 free base)
T8957L2308510-39-4
CRT0066101 dihydrochloride is an inhibitor of PKD.
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m-Hydroxybenzylpiperazine dihydrochloride
T33377L500013-37-6
m-Hydroxybenzylpiperazine dihydrochloride is a bioactive chemical.
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m-Acetotoluidide, 6'-chloro-2-(2-(diethylamino)ethyl)methylamino-, dihydrochloride
T3315277966-45-1
m-Acetotoluidide, 6'-chloro-2-(2-(diethylamino)ethyl)methylamino-, dihydrochloride is a bioactive chemical.
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m-Acetotoluidide, 2-(diethylamino)-alpha-(2-(diethylamino)acetamido)-4'-(octyloxy)-, dihydrochloride
T3314897354-58-0
m-Acetotoluidide, 2-(diethylamino)-alpha-(2-(diethylamino)acetamido)-4'-(octyloxy)-, dihydrochloride is a bioactive chemical.
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TAS-103
T36695174634-08-3
TAS-103 is a dual inhibitor of DNA topoisomerase I II, utilized in cancer research.
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RWJ-56110 dihydrochloride
T367172387505-58-8
RWJ-56110 dihydrochloride is a potent, selective, peptide-mimetic inhibitor of PAR-1 activation and internalization (binding IC50=0.44 μM), showing no effect on PAR-2, PAR-3, or PAR-4. It inhibits the aggregation of human platelets induced by SFLLRN-NH2 (IC50=0.16 μM) and thrombin (IC50=0.34 μM), with high selectivity relative to U46619. RWJ-56110 dihydrochloride also blocks angiogenesis and the formation of new vessels in vivo, and induces cell apoptosis[1][2].
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