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New Insights into the Design of Inhibitors of Human S-Adenosylmethionine Decarboxylase: Studies of Adenine C8 Substitution in Structural Analogues of S-Adenosylmethionine†
- D. McCloskey, S. Bale, +7 authors S. Ealick
- Chemistry, Medicine
- Journal of medicinal chemistry
- 11 February 2009
S-Adenosylmethionine decarboxylase (AdoMetDC) is a critical enzyme in the polyamine biosynthetic pathway and depends on a pyruvoyl group for the decarboxylation process. The crystal structures of the… Expand
Carbonic anhydrase in Tectona grandis: kinetics, stability, isozyme analysis and relationship with photosynthesis.
- A. Tiwari, P. Kumar, P. H. Chawhaan, S. Singh, S. Ansari
- Chemistry, Medicine
- Tree physiology
- 1 August 2006
Carbonic anhydrase (CA, EC: 4.2.1.1) activity in teak (Tectona grandis L.f.) was studied to determine its characteristics, kinetics and isozyme patterns. We also investigated effects of leaf age,… Expand
Inserting intrauterine devices in nulliparous women : is misoprostol beneficial ? A registered clinical trial
- P. Lotke, A. Tiwari, V. L. Nuño
- 2013
Background: To determine if misoprostol use prior to intrauterine device (IUD) insertion decreases pain and eases insertion in nulliparous women. Study Design: Nulliparous women requesting IUDs for… Expand
- 3
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Synthesis and evaluation of several new (2-chloroethyl)nitrosocarbamates as potential anticancer agents.
- R. Reynolds, A. Tiwari, +6 authors R. Struck
- Chemistry, Medicine
- Journal of medicinal chemistry
- 22 March 2000
Seven new (2-chloroethyl)nitrosocarbamates have been synthesized as potential anticancer alkylating agents. These compounds were designed with carrier moieties that would either act as prodrugs or… Expand
Conjunctival impression cytology in xerophthalmia among rural children.
- M. Singh, G. Singh, +4 authors M. Aggarwal
- Medicine
- Indian journal of ophthalmology
- 1 March 1997
The advent of Conjunctival Impression Cytology (CIC) has opened a new chapter in the detection of Vitamin A deficiency as it is a simplified field technique. The need for such a technique was of… Expand
4-Demethylpenclomedine, an antitumor-active, potentially nonneurotoxic metabolite of penclomedine.
Penclomedine [3,5-dichloro-4,6-dimethoxy-2-(trichloromethyl)pyridine], an antitumor agent, is currently in Phase I clinical trials and is believed to be a prodrug. In these studies, cerebellar… Expand
Determination of the phamacophore of penclomedine, a clinically-evaluated antitumor pyridine derivative.
The main objective of this investigation was to identify the reactive pharmacophore in penclomedine (PEN, 3,5-dichloro-4,6-dimethoxy-2-(trichloromethyl) pyridine) for in vivo antitumor activity and… Expand
Synthesis and antitumor activity of several new analogues of penclomedine and its metabolites.
- A. Tiwari, J. Riordan, W. Waud, R. Struck
- Chemistry, Medicine
- Journal of medicinal chemistry
- 31 January 2002
Analogues of penclomedine (PEN, 3,5-dichloro-4,6-dimethoxy-2-(trichloromethyl)pyridine) and its metabolites have been synthesized and evaluated as potential antitumor agents. PEN and 4-DMPEN… Expand
Chemical composition of Inula cuspidata C.B. Clarke
- C. S. Mathela, A. Tiwari, R. Padalia, C. S. Chanotiya
- Chemistry
- 1 August 2008
Thymyl isobutyrate, thymol, thymyl isovalerate, 8a-hydroxy presilphiperfolene and intermedeol have been isolated from steam volatile extract of Inula cuspidata and identified from their spectral… Expand
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Acyl derivatives of demethylpenclomedine, an antitumor-active, non-neurotoxic metabolite of penclomedine
- R. Struck, A. Tiwari, H. Friedman, Steven Keir, L. Morgan, W. Waud
- Medicine
- Cancer Chemotherapy and Pharmacology
- 1 July 2001
Abstract. Purpose: The purpose of this investigation was to compare the antitumor activities of a series of acyl derivatives of 4-demethylpenclomedine (DM-PEN), the major plasma metabolite of… Expand