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Pinoline

Pinoline
Pinoline
Molecular structure via molpic based on CDK
Physical properties
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202.25 g/mol [1]
1.5 [1]
Structural Identifiers
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C12H14N2[1]
6-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole [1]
COC1=CC2=C(C=C1)NC3=C2CCNC3 [1]
InChI=1S/C12H14N2O/c1-15-8-2-3-11-10(6-8)9-4-5-13-7-12(9)14-11/h2-3,6,13-14H,4-5,7H2,1H3 [1]
InChIKeyQYMDEOQLJUUNOF-UHFFFAOYSA-N [1]

Pinoline (also known as Pinoline, 6-methoxytryptoline, 6-Methoxy-1,2,3,4-tetrahydro-β-carboline, 1H-Pyrido[3,4-b]indole, 2,3,4,9-tetrahydro-6-methoxy-, 2,3,4,9-Tetrahydro-6-methoxy-1H-pyrido(3,4-b)indole, 1H-Pyrido(3,4-b)indole, 2,3,4,9-tetrahydro-6-methoxy-, Dtxsid30174203, 2,3,4,9-Tetrahydro-6-methoxy-1H-pyrido[3,4-b]indole, 6-methoxytetrahydronorharmane or 6-methoxy-1,2,3,4-tetrahydro β-carboline) is a substance of the β-carboline class.

Chemistry

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Pinoline is a achiral mixture.

Pharmacology

Metabolism

Subjective effects []

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 1868, Pinoline. Accessed April 29, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/1868

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Pinoline. UNII: BR3W85U4GS. Global Substance Registration System. Accessed April 29, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/BR3W85U4GS