The fungotoxicity against Botrytis cinerea of a flavonoid isolated from Pseudognaphalium robustum was analyzed. Two absorption column chromatographies and one semipreparative thin layer chromatography were used to purify the active flavonoid. It was determined, by H-NMR spectroscopy and co-elution with standards in HPLC, that this compound was 5,7-dihydroxy-3,8-dimethoxyflavone (gnaphaliin A). ...

1. The ability of exogenously administered cyclic AMP (adenosine 3': 5'-monophosphate) to exert andromimetic action on certain carbohydrate-metabolizing enzymes was investigated in the rat prostate gland and seminal vesicles. 2. Cyclic AMP, when injected concurrently with theophylline, produced marked increases in hexokinase, phosphofructokinase, glyceraldehyde phosphate dehydrogenase, pyruvate...

The synthesis and isolation in purified form of [HcyeJr-Alinsulin, a biologically active analog of sheep insulin, is described. This analog differs from the parent molecule in that the cysteine residues located at positions 6 and 11 in the A chain and participating in the formation of the intrachain cyclic system have been replaced by homocysteine residues. For the synthesis of this compound, t...

Lithium ethylene dicarbonate (CH2OCO2Li)2 was chemically synthesized and its Fourier Transform Infrared (FTIR) spectrum was obtained and compared with that of surface films formed on Ni after cyclic voltammetry (CV) in 1.2M lithium hexafluorophosphate (LiPF6)/ ethylene carbonate (EC): ethyl methyl carbonate (EMC) (3:7, w/w) electrolyte and on metallic lithium cleaved in-situ in the same electro...

A new cyclic diamine, 1,5-diazacyclohenicosane (1), was isolated from samples of the marine sponge Mycale sp. collected at Lamu Island (Kenya). Its structure was determined by a combination of spectroscopic techniques, including (+)-HRESIMS and 1D and 2D NMR spectroscopy. The compound displayed cytotoxicity at the muM level against three human tumor cell lines.

The title compound, C(34)H(54)O(5), was synthesized by the reaction of ursolic acid with ethyl chloro-acetate in the presence of DMA. All six-membered rings of the penta-cyclic triterpene skeleton adopt chair conformations. In the crystal structure, mol-ecules are linked by inter-molecular O-H⋯O hydrogen-bond inter-actions, forming zigzag chains along the c axis.

We report the synthesis of a crystalline cyclic organoboron compound that shows an anomalous Li-ion conduction behaviour with specific composition and method of insertion of a Li salt. The enhanced ionic conductivity of crystalline boric ester/LiTFSI prepared by the grinding method should be due to the formation of regulated ion-conduction channels scaffolded by boron-anion interaction.

In the crystal structure of the title compound, C(21)H(18)N(2)O(2), mol-ecules are linked through C-H⋯O inter-actions. Two symmetry-related mol-ecules form a cyclic centrosymmetric R(2) (2)(20) dimer. These dimers are further connected into chains running along the b axis.

In the title compound, C(16)H(24)NO(+)·Br(-)·C(20)H(14)O(2), the N-hetero-cyclic six-membered ring assumes a half-chair conformation. The two naphthalene ring systems are nearly perpendicular to one another, making a dihedral angle of 89.5 (2)°. Inter-molecular O-H⋯Br hydrogen bonding helps to stabilize the crystal structure.

In the title compound, C(18)H(16)N(2)O(2), the hy-droxy-ethanimine group is essentially coplanar with the ring to which it is attached (C-C-N-O torsion angle = -176.9°). Mol-ecules are linked into cyclic centrosymmetric R(2) (2)(6) dimers via O-H⋯N hydrogen bonds.