1.0 2010-04-08 22:05:15 UTC 2020-02-24 19:10:25 UTC FDB002121 Coreximine Alkaloid from Papaver somniferum (opium poppy). Coreximine is found in soursop. (-)-coreximine Alkaloid F29 Coramine Coreximine C19H21NO4 327.3743 327.147058165 3,10-dimethoxy-7,8,12b,13-tetrahydro-5H-6-azatetraphene-2,11-diol coreximine 483-45-4 COC1=C(O)C=C2C3CC4=CC(O)=C(OC)C=C4CN3CCC2=C1 InChI=1S/C19H21NO4/c1-23-18-7-11-3-4-20-10-13-8-19(24-2)16(21)6-12(13)5-15(20)14(11)9-17(18)22/h6-9,15,21-22H,3-5,10H2,1-2H3 BWUQAWCUJMATJS-UHFFFAOYSA-N belongs to the class of organic compounds known as protoberberine alkaloids and derivatives. These are alkaloids with a structure based on a protoberberine moiety, which consists of a 5,6-dihydrodibenzene moiety fused to a quinolizinium and forming 5,6-Dihydrodibenzo(a,g)quinolizinium skeleton. Protoberberine alkaloids and derivatives Organic compounds Alkaloids and derivatives Protoberberine alkaloids and derivatives Aromatic heteropolycyclic compounds 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Anisoles Aralkylamines Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Tetrahydroisoquinolines Trialkylamines 1-hydroxy-2-unsubstituted benzenoid Alkyl aryl ether Amine Anisole Aralkylamine Aromatic heteropolycyclic compound Azacycle Benzenoid Ether Hydrocarbon derivative Organic nitrogen compound Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Protoberberine skeleton Tertiary aliphatic amine Tertiary amine Tetrahydroisoquinoline Tetrahydroprotoberberine skeleton logp 2.27 ALOGPS logs -3.08 ALOGPS solubility 2.74e-01 g/l ALOGPS melting_point Mp 254-256° logp 2.86 ChemAxon pka_strongest_acidic 9.14 ChemAxon pka_strongest_basic 5.4 ChemAxon iupac 3,10-dimethoxy-7,8,12b,13-tetrahydro-5H-6-azatetraphene-2,11-diol ChemAxon average_mass 327.3743 ChemAxon mono_mass 327.147058165 ChemAxon smiles COC1=C(O)C=C2C3CC4=CC(O)=C(OC)C=C4CN3CCC2=C1 ChemAxon formula C19H21NO4 ChemAxon inchi InChI=1S/C19H21NO4/c1-23-18-7-11-3-4-20-10-13-8-19(24-2)16(21)6-12(13)5-15(20)14(11)9-17(18)22/h6-9,15,21-22H,3-5,10H2,1-2H3 ChemAxon inchikey BWUQAWCUJMATJS-UHFFFAOYSA-N ChemAxon polar_surface_area 62.16 ChemAxon refractivity 92.39 ChemAxon polarizability 35.85 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 5 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 23318 Specdb::CMs 41860 Specdb::CMs 167499 Specdb::MsMs 94185 Specdb::MsMs 94186 Specdb::MsMs 94187 Specdb::MsMs 158178 Specdb::MsMs 158179 Specdb::MsMs 158180 Specdb::MsMs 2355540 Specdb::MsMs 2355541 Specdb::MsMs 2355542 Specdb::MsMs 2607054 Specdb::MsMs 2607055 Specdb::MsMs 2607056 HMDB30286 #<Reference:0x000055ce315c3258> Soursop Type 1 specific Annona muricata 13337