Rabindranath Mukherjee

New bioactive aromatic compounds from Vismia guianensis

Five benzophenones, vismiaguianones A-E, and two benzocoumarins, vismiaguianins A and B were isolated from the CHCl3 extract of the roots of Vismia guianensis by bioassay-directed fractionation using the DNA strand-scission assay and KB cell line. Of the isolates obtained, vismiaguianone B exhibited DNA strand-scission activity, whereas vismiaguianones D and E and vismiaguianin A were found to be significantly cytotoxic.

Cytotoxic constituents from the roots of Tovomita brevistaminea.

Two known xanthones, trapezifolixanthone and manglexanthone were isolated as cytotoxic constituents from the CHCl3 extract of the roots of Tovomita brevistaminea by bioassay-guided fractionation using the KB cell line. In addition, a new compound, tovophenone C, and two known compounds, tovophenones A and B which are benzophenones, were found to be inactive constituents in this investigation. The structure of the new isolate was determined by detailed analysis of spectroscopic parameters including its 1D and 2D NMR spectroscopy data.

Hypotensive and spasmolytic effects of normacusine B from Strychnos atlantica root.

Normacusine B, a tertiary indole alkaloid, was isolated in pure form from the root bark of Strychnos atlantica Krukoff & Barneby. In conscious unrestrained rats, normacusine B (1 mg/kg) decreased the mean arterial blood pressure (27.6 ± 8.4 mmHg, n = 6), followed by a significant increase in heart rate (115.0 ± 12.7 bpm, n = 6). The alkaloid failed to induce tachycardia directly in isolated perfused rat heart. In isolated rat aortic rings, normacusine B antagonized phenylephrine and serotonin-induced contractions. Schild plot analysis of individual cumulative concentration-response curves was compatible with a competitive type of antagonism against phenylephrine (pA(2) = 7.05 ± 0.11) and of a non-competitive nature against 5-hydroxytryptamine (apparent pA(2) = 7.02 ± 0.08). Normacusine B was found inactive against KCl and PGF(2α) induced contractions.

Structure and stereochemistry of divarine: another new bisindole alkaloid from Strychnos divaricans ducke

The complete stereostructure of divaricine, a new bisindole alkaloid from Srychnos divaricans Ducke., has been determined mainly by the use of one- and two-dimensional nmr techniques

Stereoconfiguration of sequoyitol by high resolution 1H NMR

Abstract The stereoconfiguration of sequoyitol, isolated as the pentaacetate from the leaves of Podocarpus sellowii , has been established by comparing its 1 H NMR spectrum with that of myo -inositol hexaacetate.