1.0 2010-04-08 22:09:26 UTC 2018-05-28 23:29:27 UTC FDB011053 Piperolactam A Alkaloid from roots of Piper longum (long pepper). 1-Hydroxy-2-methoxy-dibenz(cd,F)indol-4(5H)-one 1-Hydroxy-2-methoxy-dibenz[cd,F]indol-4(5H)-one 1-Hydroxy-2-methoxydibenz(cd,f)indol-4(5H)-one 1-Hydroxy-2-methoxydibenz[cd,f]indol-4(5H)-one, 9CI Aristolactam F1 Dibenz(cd,f)indol-4(5H)-one, 1-hydroxy-2-methoxy- Dibenz[cd,f]indol-4(5H)-one, 1-hydroxy-2-methoxy- Piperolactam A C16H11NO3 265.2634 265.073893223 15-hydroxy-14-methoxy-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2(7),3,5,8,12(16),13-heptaen-11-one 15-hydroxy-14-methoxy-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2(7),3,5,8,12(16),13-heptaen-11-one 112501-42-5 COC1=CC2=C3C(NC2=O)=CC2=C(C=CC=C2)C3=C1O InChI=1S/C16H11NO3/c1-20-12-7-10-13-11(17-16(10)19)6-8-4-2-3-5-9(8)14(13)15(12)18/h2-7,18H,1H3,(H,17,19) KBGNBPGXVKPRQI-UHFFFAOYSA-N belongs to the class of organic compounds known as aristolactams. These are phenanthrenic compounds containing a five-membered lactam ring and a 1,3-dioxolane ring fused to the phenanthrene ring system. Aristolactams Organic compounds Alkaloids and derivatives Aristolactams Aromatic heteropolycyclic compounds Alkyl aryl ethers Anisoles Azacyclic compounds Hydrocarbon derivatives Indoles and derivatives Isoindolones Lactams Naphthols and derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Phenanthrols Secondary carboxylic acid amides 1-naphthol Alkyl aryl ether Anisole Aristolactam Aromatic heteropolycyclic compound Azacycle Benzenoid Carboxamide group Carboxylic acid derivative Ether Hydrocarbon derivative Indole or derivatives Isoindole or derivatives Isoindolone Lactam Naphthalene Organic nitrogen compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenanthrene Phenanthrol Secondary carboxylic acid amide logp 2.94 ALOGPS logs -3.55 ALOGPS solubility 7.42e-02 g/l ALOGPS melting_point Mp 303-306 dec. (271-273°) logp 2.61 ChemAxon pka_strongest_acidic 8.56 ChemAxon pka_strongest_basic -4.2 ChemAxon iupac 15-hydroxy-14-methoxy-10-azatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(15),2(7),3,5,8,12(16),13-heptaen-11-one ChemAxon average_mass 265.2634 ChemAxon mono_mass 265.073893223 ChemAxon smiles COC1=CC2=C3C(NC2=O)=CC2=C(C=CC=C2)C3=C1O ChemAxon formula C16H11NO3 ChemAxon inchi InChI=1S/C16H11NO3/c1-20-12-7-10-13-11(17-16(10)19)6-8-4-2-3-5-9(8)14(13)15(12)18/h2-7,18H,1H3,(H,17,19) ChemAxon inchikey KBGNBPGXVKPRQI-UHFFFAOYSA-N ChemAxon polar_surface_area 58.56 ChemAxon refractivity 76.88 ChemAxon polarizability 27.37 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 3 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 15040 Specdb::CMs 43072 Specdb::CMs 154622 Specdb::MsMs 87300 Specdb::MsMs 87301 Specdb::MsMs 87302 Specdb::MsMs 149775 Specdb::MsMs 149776 Specdb::MsMs 149777 Specdb::MsMs 2659708 Specdb::MsMs 2659709 Specdb::MsMs 2659710 Specdb::MsMs 3019713 Specdb::MsMs 3019714 Specdb::MsMs 3019715 HMDB33060 #<Reference:0x000055ce31a6a9c8>