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| Ranju BansalSummaryCountry: India Publications
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Publications
Synthesis and antileukemic activity of 16E-[4-(2-carboxy)ethoxybenzylidene]-androstene amidesRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160 014, India
Steroids 77:552-7. 2012..94, 2.61, 6.90 and 1.79μM against CCRF-CEM, K-562, RPMI-8226 and SR leukemia cell lines, respectively...
Synthesis and aromatase inhibitory activity of some new 16E-arylidenosteroidsRanju Bansal
University Institute of Pharmaceutical Sciences, Sector 14, Panjab University, Chandigarh 160 014, India Electronic address
Bioorg Chem 45:36-40. 2012..2μM) and 16-(benzo-[1,3]dioxol-5-ylmethylene)androsta-1,4-diene-3,17-dione (11, IC(50): 6.4μM) were found to be approximately five times more potent in comparison to aminoglutethimide...
Synthesis and anticonvulsant activity of O-alkylated derivatives of 1-(2-naphthyl)-2-(imidazol-1-yl)ethanone oximeR Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, India
Arzneimittelforschung 62:420-4. 2012..Anticonvulsant activity of the compounds was determined against pentylenetetrazole induced convulsions in mice. The newly synthesized compounds exhibited moderate to significant activity compared to diazepam...
Design, synthesis and evaluation of novel 16-imidazolyl substituted steroidal derivatives possessing potent diversified pharmacological propertiesRanju Bansal
University Institute of Pharmaceutical Sciences, Sector 14, Panjab University, Chandigarh 160014, India
Steroids 77:621-9. 2012..9 μm)...
Synthesis of a new series of 1H-imidazol-1-yl substituted 8-phenylxanthines as adenosine receptor ligandsRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Chem Biodivers 8:1290-300. 2011..The xanthine derivatives displayed varying degrees of affinity and selectivity towards A(1) and A(2A) receptor subtypes despite a common but variedly substituted Ar-C(8)...
Synthesis and biological evaluation of 16E-arylidenosteroids as cytotoxic and anti-aromatase agentsRanju Bansal
University Institute of Pharmaceutical Sciences, Sector 14, Panjab University, Chandigarh, India
Chem Pharm Bull (Tokyo) 59:327-31. 2011....
Synthesis of quaternary ammonium salts of 16E-[4-(2-alkylaminoethoxy)-3-methoxybenzylidene]androstene derivatives as skeletal muscle relaxantsRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, India
Steroids 76:254-60. 2011..Some of the compounds also inhibited acetylcholinesterase activity in low concentrations so that they would not be directly suitable for use as muscle relaxants...
Synthesis of 8-(cyclopentyloxy)phenyl substituted xanthine derivatives as adenosine A2A ligandsRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Arzneimittelforschung 60:131-6. 2010....
Synthesis and antineoplastic activity of O-alkylated derivatives of 7-hydroximinoandrost-5-ene steroidsRanju Bansal
University Institute of Pharmaceutical Sciences, Sector 14, Panjab University, Chandigarh, India
Arch Pharm (Weinheim) 343:377-83. 2010..However, the imidazolyl-substituted steroidal oxime ethers displayed moderate inhibition of cytochrome P450 aromatase...
Synthesis and vasodilatory activity of some amide derivatives of 6-(4-carboxymethyloxyphenyl)-4,5-dihydro-3(2H)-pyridazinoneRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Sector 14, Chandigarh 160014, India
Eur J Med Chem 44:4441-7. 2009..The most active compound 6-[4-(2-oxo-2-pyrrolidin-1-yl-ethoxy)phenyl]-2-(4-fluorophenyl)-4,5-dihydropyridazin-3(2H)-one (11) exhibited vasodilating activity in nanomolar range (IC(50)=0.051 microM)...
Synthesis of 16E-[3-methoxy-4-(2-aminoethoxy)benzylidene]androstene derivatives as potent cytotoxic agentsRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Steroids 73:1391-9. 2008....
An update on cyclic nucleotide phosphodiesterase (PDE) inhibitors: phosphodiesterases and drug selectivityR Gupta
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Methods Find Exp Clin Pharmacol 27:101-18. 2005..This review details many key aspects of multiple forms of PDEs and their inhibitors with diversified chemical structures, which can act as leads for synthesis of novel drugs...
Corticosteroids: the mainstay in asthma therapyRanju Gupta
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Bioorg Med Chem 12:6331-42. 2004....
Synthesis and evaluation of a dimer of 2-(4-pyridylmethyl)-1-indanone as a novel nonsteroidal aromatase inhibitorRanju Gupta
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, India
Arch Pharm (Weinheim) 337:398-401. 2004..The dimer showed strong inhibition of human placental aromatase and was found 3 times more potent (RP = 3, IC(50) = 10.2 microM) as compared to aminoglutethimide (RP = 1, IC(50) = 18.5 microM...
Synthesis and study of some new N-substituted imide derivatives as potential anticancer agentsDharam Paul Jindal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh-160014, India
Farmaco 60:283-90. 2005..These compounds (37-39) have exhibited weak inhibition of human placental aromatase as compared to aminoglutethimide...
Synthesis of a series of 8-(substituted-phenyl)xanthines and a study on the effects of substitution pattern of phenyl substituents on affinity for adenosine A(1) and A(2A) receptorsRanju Bansal
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Eur J Med Chem 44:2122-7. 2009..It has been observed that substitution pattern on 8-phenyl group greatly affects the affinity and selectivity at adenosine receptors, with A(2A) tolerating bulkier substituents than did A(1) receptors...
Synthesis and evaluation of 2-substituted-6-phenyl-4,5-dihydropyridazin-3(2H)-ones as potent inodilatorsDinesh Kumar
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160014, India
Acta Pharm 58:393-405. 2008..6-(4-Methanesulfonamidophenyl)-2-phenyl-4,5-dihydropyridazin-3(2H)-one (7) exhibited significant inodilatory properties and showed vasorelaxant activity in a nanomolar range (IC50 = 0.08 +/- 0.01 mumol L-1)...
Synthesis and bronchodilatory activity of some nitrogen bridgehead compoundsDharam Paul Jindal
University Institute of Pharmaceutical Sciences formerly Department of Pharmaceutical Sciences, Panjab University, Chandigarh 160 014, India
Eur J Med Chem 37:419-25. 2002..This resulted in loss of relaxation activity in precontracted guinea pig tracheal chain. These results show that the better relaxation property possessed by compound 7 hydrochloride is due to methoxy groups at 8 and 9 positions...
