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Showing papers by "Kirpal S. Bisht published in 1995"


Journal ArticleDOI
TL;DR: In this article, a lignan and three neolignans were identified from the leaves and stems of Piper clarkii and their structures were established on the basis of 1 H, 13 C and 1 H 1 H COSY NMR, NOE and mass spectral data and CD curves.

25 citations



Journal ArticleDOI
TL;DR: Tyagi et al. as mentioned in this paper proposed a new neolignan, (7R,8S,1 'S)-A, from Piper schmidtii and reassignment of the structure of Schmiditin.
Abstract: Department of Chemistry, University of Delhi, Delhi-11 0 007, India Tyagi, 0. D., Prasad, A. K., Wengel, J., Boll, P.M., Olsen, C. E., Parmar, V. S., Sharma, N. K., Jha, A. and Bisht, K. S., 1995. Neolignans from Piper schmidtii and Reassignment of the Structure of Schmiditin. - Acta Chern. Scand. 49: 142 -148 © Acta Chemica Scandinavica 1995. A new neolignan, (7R,8S,1 'S)-A

12 citations


Journal ArticleDOI
TL;DR: In this article, a new benzoic acid ester, 2-E-[2″-oxo-cyclopent-3″-en-1″-ylidene]ethyl benzoate, together with tritriacontane, tetratriacontanol and β-sitosterol have been isolated from a petrol extract of the leaves of Uvaria narum.

11 citations



Journal ArticleDOI
TL;DR: Several compounds from Piper species bearing methylenedioxyphenyl moieties are reported for the first time to effectively inhibit the rat liver microsome-mediated aflatoxin B1-DNA binding in vitro.

3 citations



Journal ArticleDOI
TL;DR: In the title compound, C 24 H 15 BrN 2 O 2, the angles formed by the planes of the bromophenyl, phenyl and coumarin groups with the plane of the pyrazole nucleus are 19.3, 38.8 and 65.6°, respectively as discussed by the authors.
Abstract: In the title compound, C 24 H 15 BrN 2 O 2 , the angles formed by the planes of the bromophenyl, phenyl and coumarin groups with the plane of the pyrazole nucleus are 19.3, 38.8 and 65.6°, respectively. The absolute structure has been determined.

Journal ArticleDOI
TL;DR: Several compounds from Piper species bearing methylenedioxyphenyl moieties were reported for the first time to effectively inhibit the rat liver microsome-mediated aflatoxin B1-DNA binding in vitro as mentioned in this paper.
Abstract: Several compounds from Piper species bearing methylenedioxyphenyl moieties are reported for the first time to effectively inhibit the rat liver microsome-mediated aflatoxin B1-DNA binding in vitro. From the preliminary results obtained, a structure-activity relationship is proposed.