302440 <common-name>(2s)-2-amino-n-(4-methoxynaphthalen-2-yl)-3-methylbutanamide</common-name> <description>(2s)-2-amino-n-(4-methoxynaphthalen-2-yl)-3-methylbutanamide belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. It has the formula C16H20N2O2 and an average molecular weight of 272.34 g/mol.</description> <cas nil="true"/> <pubchem-id>7021444</pubchem-id> <chemical-formula>C16H20N2O2</chemical-formula> <weight>272.34</weight> <appearance nil="true"/> <melting-point nil="true"/> <boiling-point nil="true"/> <density nil="true"/> <solubility nil="true"/> <specific-gravity nil="true"/> <flash-point nil="true"/> <vapour-pressure nil="true"/> <route-of-exposure nil="true"/> <target nil="true"/> <mechanism-of-toxicity nil="true"/> <metabolism nil="true"/> <toxicity nil="true"/> <lethaldose nil="true"/> <carcinogenicity nil="true"/> <use-source nil="true"/> <min-risk-level nil="true"/> <health-effects nil="true"/> <symptoms nil="true"/> <treatment nil="true"/> <created-at type="dateTime">2026-08-28T19:31:13Z</created-at> <updated-at type="dateTime">2026-08-28T19:31:13Z</updated-at> <interacting-proteins nil="true"/> <wikipedia nil="true"/> <uniprot-id nil="true"/> <kegg-compound-id nil="true"/> <omim-id nil="true"/> <chebi-id nil="true"/> <biocyc-id nil="true"/> <ctd-id nil="true"/> <stitch-id nil="true"/> <drugbank-id nil="true"/> <pdb-id nil="true"/> <actor-id nil="true"/> <organism nil="true"/> <export type="boolean">true</export> <metabolizing-proteins nil="true"/> <transporting-proteins nil="true"/> <moldb-smiles>CC(C)C(C(=O)NC1=CC2=CC=CC=C2C(=C1)OC)N</moldb-smiles> <moldb-formula>C16H20N2O2</moldb-formula> <moldb-inchi>InChI=1S/C16H20N2O2/c1-10(2)15(17)16(19)18-12-8-11-6-4-5-7-13(11)14(9-12)20-3/h4-10,15H,17H2,1-3H3,(H,18,19)/t15-/m0/s1</moldb-inchi> <moldb-inchikey>GRDPQPREOTZYRW-HNNXBMFYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">272.1524779</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>2.8</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id nil="true"/> <structure-image-file-name nil="true"/> <structure-image-content-type nil="true"/> <structure-image-file-size type="integer" nil="true"/> <structure-image-updated-at type="dateTime" nil="true"/> <biodb-id nil="true"/> <synthesis-reference nil="true"/> <structure-image-caption nil="true"/> <chemdb-id>CHEM298333</chemdb-id> <dsstox-id nil="true"/> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id nil="true"/> <iupac>(2s)-2-amino-n-(4-methoxynaphthalen-2-yl)-3-methylbutanamide</iupac> <moldb-polar-surface-area nil="true"/> <moldb-refractivity nil="true"/> <moldb-polarizability nil="true"/> <moldb-rotatable-bond-count nil="true"/> <moldb-acceptor-count nil="true"/> <moldb-donor-count nil="true"/> <moldb-pka-strongest-acidic nil="true"/> <moldb-pka-strongest-basic nil="true"/> <moldb-physiological-charge nil="true"/> <moldb-number-of-rings nil="true"/> <moldb-alogps-logp nil="true"/> <moldb-alogps-logs nil="true"/> <moldb-alogps-solubility nil="true"/> <kingdom>Organic compounds</kingdom> <superklass>Organic acids and derivatives</superklass> <klass>Carboxylic acids and derivatives</klass> <subklass>Amino acids, peptides, and analogues</subklass> <paper-count type="integer" nil="true"/> <sync-id>CED0253658</sync-id> <structure-inchikey>GRDPQPREOTZYRW-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>40000000000000000000080000000000000000000000000180000000000000400000001000000000000000000000000000080000000000000000000000000000000000000000000400000000000000000020000000000100000001000000020000002000010000000840000008100000000000000000000000000000000000020000000040000001800000800000000080001000000100000000000000000000000000000000000000040000080000000000000000000000000000000000000080000000040000000000000000000000800000000000000000000200000400000080008000000001000040000000000400000000000020000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€���`�������`�������`�������`�������(�������(�������h�������@(������@h�������@(������@h�������@h�������@h�������@h�������@(������@(������@h��������(�������`�������`��������������������(��� �� ��h�� h� h� �h���h�� h� �h���h���h��� ��������h�� h�B��������� �� �� � ����������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T05:11:52Z</structure-indexed-at> </compound>