Publication | Open Access
Facile synthesis of substituted trans-2-arylcyclopropylamine inhibitors of the human histone demethylase LSD1 and monoamine oxidases A and B
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References
2008
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Molecular PharmacologyMedicinal ChemistryBiochemistryMedicineFacile SynthesisNatural SciencesSubstituted Trans-2-arylcyclopropylamine InhibitorsOrganic ChemistryPharmacologyPharmaceutical ChemistrySynthetic ChemistryDrug Discovery
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