Hayat M. Mukhtar
Hamdard University
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Publication
Featured researches published by Hayat M. Mukhtar.
Pharmaceutical Biology | 2004
Hayat M. Mukhtar; S. H. Ansari; Mohd Ali; T. Naved
A lanostane-type triterpene, zizyphulanostane-21-oic acid, and a terpenic δ-lactone, zizyphulanostan-18-oic acid, have been isolated from the roots of Zizyphus vulgaris Lam. (syn. Z. sativa Gaertn., Z. mauritina. Lam.) and characterized as lanosta-25 (26)-en-9α-ol-21-oic acid and lanosta-25 (26)-en-22β-ol-18-oic acid 3(19)-olide, respectively, on the basis of spectroscopic techniques and chemical means.
Pharmaceutical Biology | 2006
Hayat M. Mukhtar; S. H. Ansari; Z. A. Bhat; T. Naved
Abstract The effect of administering an ethanol extract of Cyamopsis tetragonoloba. Linn. (Leguminosae) beans on blood glucose levels in normal and alloxan-induced diabetic rats was evaluated in this study. The ethanol extract of beans at 250 mg/kg body weight significantly reduced the blood glucose levels in alloxan-induced diabetic rats within 3 h of administration. Continued administration of the extract at the same dose daily for 10 days produced a statistically significant reduction in the blood glucose levels, whereas marginal activity was seen in normal and glucose-loaded rats.
Pharmaceutical Biology | 2005
Hayat M. Mukhtar; S. H. Ansari; Mohd Ali; T. Naved; Z. A. Bhat
Abstract Two new ursane-type triterpenes, zizyphursolic acid (1), and isozizyphursolic acid (2), have been isolated from the roots of Zizyphus vulgaris. Lam. (syn: Z. sativa. Gaertn.; Z. mauritiana. Lamk.) and characterized as 18β.H-urs-20 (30)-en-3β.-ol-28-oic acid and 18β.H-urs-20 (30)-en-2α.-ol-28-oic acid, respectively. Their structures were elucidated by spectroscopic (UV, IR, NMR, and MS) methods and chemical reactions.
Pharmaceutical Biology | 2004
Hayat M. Mukhtar; S. H. Ansari; Mohd Ali; T. Naved
A new δ-lactone containing triterpene, 4β-methylcholest-20-en-12a-ol-3β-olide, was isolated from Calendula officinalis Linn. flowers in addition to three known compounds, lanast-20(22)-en-3β-ol, stigmast-5,22-dien-3β-ol, and stigmast-5,24(28)-dien-3β-ol. Their structures were elucidated by spectroscopic (UV, IR, NMR, and MS) methods and chemical reactions.
Die Pharmazie | 2005
Hayat M. Mukhtar; Ansari Sh; Mushir Ali; Bhat Za; T. Naved
Die Pharmazie | 2004
Hayat M. Mukhtar; Ansari Sh; Mushir Ali; T. Naved; Bhat Za
Die Pharmazie | 2005
Bhat Za; Ansari Sh; Hayat M. Mukhtar; T. Naved; Siddiqui Ji; Khan Na
Journal of Natural Remedies | 2004
Hayat M. Mukhtar; S. H. Ansari; Mohd Ali; T. Naved; Z. A. Bhat
Journal of Natural Remedies | 2005
T. Naved; Javed Inam Siddiqui; S. H. Ansari; Anis A. Ansari; Hayat M. Mukhtar
Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry | 2005
T. Naved; S. H. Ansari; Hayat M. Mukhtar; Mushir Ali