1.0 2026-09-22 00:51:08 UTC 2026-09-22 00:51:08 UTC FDB117421 lycorine (1S,17S,18S,19S)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol C16H17NO4 287.3105 287.115758037 (1S,17S,18S,19S)-5,7-dioxa-12-azapentacyclo[10.6.1.0^{2,10}.0^{4,8}.0^{15,19}]nonadeca-2,4(8),9,15-tetraene-17,18-diol (1S,17S,18S,19S)-5,7-dioxa-12-azapentacyclo[10.6.1.0^{2,10}.0^{4,8}.0^{15,19}]nonadeca-2,4(8),9,15-tetraene-17,18-diol [H][C@@]12N3CCC1=C[C@H](O)[C@@H](O)[C@@]2([H])C1=CC2=C(OCO2)C=C1C3 InChI=1S/C16H17NO4/c18-11-3-8-1-2-17-6-9-4-12-13(21-7-20-12)5-10(9)14(15(8)17)16(11)19/h3-5,11,14-16,18-19H,1-2,6-7H2/t11-,14-,15+,16+/m0/s1 XGVJWXAYKUHDOO-DANNLKNASA-N belongs to the class of organic compounds known as lycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the lycorine skeleton, made up of a pyrrolo[d,e]phenanthridine ring system. Lycorine-type amaryllidaceae alkaloids Organic compounds Alkaloids and derivatives Amaryllidaceae alkaloids Lycorine-type amaryllidaceae alkaloids Aromatic heteropolycyclic compounds 1,2-diols Acetals Aralkylamines Azacyclic compounds Benzenoids Benzodioxoles Hydrocarbon derivatives Indoles and derivatives N-alkylpyrrolidines Organopnictogen compounds Oxacyclic compounds Phenanthridines and derivatives Secondary alcohols Tetrahydroisoquinolines Trialkylamines 1,2-diol Acetal Alcohol Amine Aralkylamine Aromatic heteropolycyclic compound Azacycle Benzenoid Benzodioxole Benzoquinoline Hydrocarbon derivative Indole or derivatives Lycorine skeleton N-alkylpyrrolidine Organic nitrogen compound Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Oxacycle Phenanthridine Pyrrolidine Quinoline Secondary alcohol Tertiary aliphatic amine Tertiary amine Tetrahydroisoquinoline Isoquinoline alkaloids indolizidine alkaloid logp 0.01 ALOGPS logs -1.59 ALOGPS solubility 7.43e+00 g/l ALOGPS logp 0.16 ChemAxon pka_strongest_acidic 13.46 ChemAxon pka_strongest_basic 7.82 ChemAxon iupac (1S,17S,18S,19S)-5,7-dioxa-12-azapentacyclo[10.6.1.0^{2,10}.0^{4,8}.0^{15,19}]nonadeca-2,4(8),9,15-tetraene-17,18-diol ChemAxon average_mass 287.3105 ChemAxon mono_mass 287.115758037 ChemAxon smiles [H][C@@]12N3CCC1=C[C@H](O)[C@@H](O)[C@@]2([H])C1=CC2=C(OCO2)C=C1C3 ChemAxon formula C16H17NO4 ChemAxon inchi InChI=1S/C16H17NO4/c18-11-3-8-1-2-17-6-9-4-12-13(21-7-20-12)5-10(9)14(15(8)17)16(11)19/h3-5,11,14-16,18-19H,1-2,6-7H2/t11-,14-,15+,16+/m0/s1 ChemAxon inchikey XGVJWXAYKUHDOO-DANNLKNASA-N ChemAxon polar_surface_area 62.16 ChemAxon refractivity 76.18 ChemAxon polarizability 30.04 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 5 ChemAxon donor_count 2 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 55032 Specdb::MsMs 55033 Specdb::MsMs 55034 Specdb::MsMs 125835 Specdb::MsMs 125836 Specdb::MsMs 125837