1.0 2010-04-08 22:10:17 UTC 2019-11-26 03:07:19 UTC FDB012658 Cordeauxione Isolated from leaf hairs of Cordeauxia edulis (yehib). Cordeauxione is found in nuts. 2-Acetyl-4,7,8-trihydroxy-6-methoxy-3-methyl-1,5-naphthalenedione, 9CI 5,11-Dimethyl-6H-pyrido(4,3-b)carbazole 5,11-Dimethyl-6H-pyrido[4,3-b]carbazole 6H-Pyrido(4,3-b)carbazole, 5,11-dimethyl- 6H-Pyrido[4,3-b]carbazole, 5,11-dimethyl- 7-Acetyl-2,5,8-trihydroxy-3-methoxy-6-methyl-1,4-naphthoquinone Celiptium Cordeauxiaquinone Ellipticine Ellipticine, monohydrochloride Elliptisine C14H12O7 292.2409 292.058302738 2-acetyl-4,7,8-trihydroxy-6-methoxy-3-methyl-1,5-dihydronaphthalene-1,5-dione 2-acetyl-4,7,8-trihydroxy-6-methoxy-3-methylnaphthalene-1,5-dione 1228-77-9 COC1=C(O)C(O)=C2C(=O)C(C(C)=O)=C(C)C(O)=C2C1=O InChI=1S/C14H12O7/c1-4-6(5(2)15)10(17)8-7(9(4)16)12(19)14(21-3)13(20)11(8)18/h16,18,20H,1-3H3 HHMBLIVHBTZFJR-UHFFFAOYSA-N belongs to the class of organic compounds known as vinylogous acids. These are organic compounds containing a hydroxyl group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety. Vinylogous acids Organic compounds Organic acids and derivatives Vinylogous acids Aliphatic homopolycyclic compounds Enols Hydrocarbon derivatives Ketones Organic oxides Polyols Aliphatic homopolycyclic compound Carbonyl group Enol Hydrocarbon derivative Ketone Organic oxide Organic oxygen compound Organooxygen compound Polyol Vinylogous acid logp -0.05 ALOGPS logs -2.81 ALOGPS solubility 4.53e-01 g/l ALOGPS melting_point Mp 194° logp -0.74 ChemAxon pka_strongest_acidic 5.89 ChemAxon pka_strongest_basic -5 ChemAxon iupac 2-acetyl-4,7,8-trihydroxy-6-methoxy-3-methyl-1,5-dihydronaphthalene-1,5-dione ChemAxon average_mass 292.2409 ChemAxon mono_mass 292.058302738 ChemAxon smiles COC1=C(O)C(O)=C2C(=O)C(C(C)=O)=C(C)C(O)=C2C1=O ChemAxon formula C14H12O7 ChemAxon inchi InChI=1S/C14H12O7/c1-4-6(5(2)15)10(17)8-7(9(4)16)12(19)14(21-3)13(20)11(8)18/h16,18,20H,1-3H3 ChemAxon inchikey HHMBLIVHBTZFJR-UHFFFAOYSA-N ChemAxon polar_surface_area 121.13 ChemAxon refractivity 75.68 ChemAxon polarizability 27.44 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 7 ChemAxon donor_count 3 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 15360 Specdb::CMs 43807 Specdb::CMs 146793 Specdb::NmrOneD 125658 Specdb::NmrOneD 125659 Specdb::NmrOneD 125660 Specdb::NmrOneD 125661 Specdb::NmrOneD 125662 Specdb::NmrOneD 125663 Specdb::NmrOneD 125664 Specdb::NmrOneD 125665 Specdb::NmrOneD 125666 Specdb::NmrOneD 125667 Specdb::NmrOneD 125668 Specdb::NmrOneD 125669 Specdb::NmrOneD 125670 Specdb::NmrOneD 125671 Specdb::NmrOneD 125672 Specdb::NmrOneD 125673 Specdb::NmrOneD 125674 Specdb::NmrOneD 125675 Specdb::NmrOneD 125676 Specdb::NmrOneD 125677 Specdb::MsMs 109539 Specdb::MsMs 109540 Specdb::MsMs 109541 Specdb::MsMs 176991 Specdb::MsMs 176992 Specdb::MsMs 176993 Specdb::MsMs 2675989 Specdb::MsMs 2675990 Specdb::MsMs 2675991 Specdb::MsMs 3028979 Specdb::MsMs 3028980 Specdb::MsMs 3028981 HMDB34310 #<Reference:0x000055ce315f7bc0> Nuts Unknown generic