Anodyne

Aptiganel
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Aptiganel hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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303.4 g/mol [1]
4.6 [1]
Structural Identifiers
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C20H21N3 [1]
1-(3-ethylphenyl)-1-methyl-2-naphthalen-1-ylguanidine [1]
CCC1=CC(=CC=C1)N(C)C(=NC2=CC=CC3=CC=CC=C32)N [1]
InChI=1S/C20H21N3/c1-3-15-8-6-11-17(14-15)23(2)20(21)22-19-13-7-10-16-9-4-5-12-18(16)19/h4-14H,3H2,1-2H3,(H2,21,22) [1]
InChIKeyBFNCJMURTMZBTE-UHFFFAOYSA-N [1]

Aptiganel

Aptiganel (also known as 1-(m-Ethylphenyl)-1-methyl-3-(1-naphthyl)guanidine, Guanidine, N-(3-ethylphenyl)-N-methyl-N'-1-naphthalenyl, aptiganelum, RefChem:113564, 1-(3-ethylphenyl)-1-methyl-3-(naphthalen-1-yl)guanidine, Guanidine, N-(3-ethylphenyl)-N-methyl-N'-1-naphthalenyl-, Lopac-C-4238, Lopac0_000312, orb1701185 or CCG-204407) is a substance of the benzylamine class.

Chemistry

Salts []

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

 []

Aptiganel is a achiral mixture

Anodyne Usernotes
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magnus / Aptiganel -

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 60840, Aptiganel. Accessed September 1, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/60840

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Aptiganel. UNII: 46475LV84I. Global Substance Registration System. Accessed September 1, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/46475LV84I