Anodyne

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Pagoclone
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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407.9 g/mol [1]
4.6 [1]
Structural Identifiers
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C23H22ClN3O2 [1]
2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)-3H-isoindol-1-one [1]
CC(C)CCC(=O)CC1C2=CC=CC=C2C(=O)N1C3=NC4=C(C=C3)C=CC(=N4)Cl [1]
InChI=1S/C23H22ClN3O2/c1-14(2)7-10-16(28)13-19-17-5-3-4-6-18(17)23(29)27(19)21-12-9-15-8-11-20(24)25-22(15)26-21/h3-6,8-9,11-12,14,19H,7,10,13H2,1-2H3 [1]
InChIKeyHIUPRQPBWVEQJJ-UHFFFAOYSA-N [1]

Pagoclone

Pagoclone (also known as IP 456, Pagoclona, IP-456, CI-1043, RP 62955, RP-62955, 2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)-2,3-dihydro-1H-isoindol-1-one, 38VAG2SA33, pagoclonum or IP456) is a substance of the racetam class.

Chemistry

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Pagoclone is a racemic mixture of the

Stereoisomers
(R)-PagocloneGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-PagocloneGenerated by the Chemistry Development Kit (http://github.com/cdk)
Anodyne Usernotes
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magnus / Pagoclone via Oral -

See also []

  • Substituted racetams
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 131664, Pagoclone. Accessed September 1, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/131664