141243 <common-name>Aseripide</common-name> <description>Aseripide belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. It has the chemical formula C26H30FN3O6S. With an average molecular weight of 531.60 g/mol, Aseripide is a heavy molecule.</description> <cas>153242-02-5</cas> <pubchem-id nil="true"/> <chemical-formula>C26H30FN3O6S</chemical-formula> <weight nil="true"/> <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">2026-04-15T17:33:56Z</created-at> <updated-at type="dateTime">2026-05-14T20:36:54Z</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>DB20702</drugbank-id> <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>C[C@H](C(O)=O)C1=CC(NC(=O)NCC(=O)N2[C@@H](CS[C@@H]2C2=CC=CC=C2F)C(=O)OC(C)(C)C)=CC=C1</moldb-smiles> <moldb-formula>C26H30FN3O6S</moldb-formula> <moldb-inchi>InChI=1S/C26H30FN3O6S/c1-15(23(32)33)16-8-7-9-17(12-16)29-25(35)28-13-21(31)30-20(24(34)36-26(2,3)4)14-37-22(30)18-10-5-6-11-19(18)27/h5-12,15,20,22H,13-14H2,1-4H3,(H,32,33)(H2,28,29,35)/t15-,20+,22+/m0/s1</moldb-inchi> <moldb-inchikey>IPIGNHDAVWQEDN-GJULWVSJSA-N</moldb-inchikey> <moldb-average-mass type="decimal">531.6</moldb-average-mass> <moldb-mono-mass type="decimal">531.183935035</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <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>CHEM137136</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 nil="true"/> <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">0</paper-count> <sync-id>CED0159917</sync-id> <structure-inchikey>IPIGNHDAVWQEDN-GJULWVSJSA-N</structure-inchikey> <structure-fingerprint>40000000000000000000800800802000000000000000008104040000010000000000001400000080000000000000100004800000000000000000000000000000000012000000000000000000000000000020000010000111000000000000001000020000010000000000000000100000080000420120000000000000020040101081000040001000800000000000000080000000000100000000000000400000000000000000400000000400080000000000000080010000000000000000000000000000020c00000000000000000000000000000000000000000200000000000000008008008800100040800020000400800020020000000600000004000000</structure-fingerprint> 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