Anodyne

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Clorgyline
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Clorgyline hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic
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Physical properties
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Molecular mass272.17 g/mol [1]
Predicted LogP4.2 [1]
Structural Identifiers
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Molecular formulaC13H15Cl2NO [1]
IUPAC name3-(2,4-dichlorophenoxy)-N-methyl-N-prop-2-ynylpropan-1-amine [1]
SMILESCN(CCCOC1=C(C=C(C=C1)Cl)Cl)CC#C [1]
InChIInChI=1S/C13H15Cl2NO/c1-3-7-16(2)8-4-9-17-13-6-5-11(14)10-12(13)15/h1,5-6,10H,4,7-9H2,2H3 [1]
InChIKeyBTFHLQRNAMSNLC-UHFFFAOYSA-N [1]
Dosing

Clorgyline

Clorgyline (also known as Clorgiline, Chlorgyline, Clorgilina, Clorgilinum, M and B 9302, M & B 9302, N-(3-(2,4-Dichlorophenoxy)propyl)-N-methyl-2-propynylamine, M&B 9302, N-(3-(2,4-dichlorophenoxy)propyl)-N-methylprop-2-yn-1-amine or 2-Propyn-1-amine, N-(3-(2,4-dichlorophenoxy)propyl)-N-methyl-) is a monoamine oxidase inhibitor substance of the phenol class.

Chemistry

Salts []

Clorgyline is typically found in the form of its hydrochloride salt.

See also []

  • Substituted phenols
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 4380, Clorgyline. Accessed July 20, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4380

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Clorgyline. UNII: LYJ16FZU9Q. Global Substance Registration System. Accessed July 20, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/LYJ16FZU9Q