Synthesis and antimicrobial studies of chalconyl pregnenolones

[1]  B. D. Gupta,et al.  D-ring substituted 1,2,3-triazolyl 20-keto pregnenanes as potential anticancer agents: Synthesis and biological evaluation , 2010, Steroids.

[2]  K. Suri,et al.  Studies on novel D-ring substituted steroidal pyrazolines as potential anticancer agents , 2010, Steroids.

[3]  Namdev T. Khandare,et al.  SYNTHESIS AND IN VITRO ANTIMICROBIAL ACTIVITY OF SOME NEW 1-THIAZOLYL-2-PYRAZOLINE DERIVATIVES , 2010 .

[4]  M. Alam,et al.  Synthesis of novel steroidal D-ring substituted isoxazoline derivatives of 17-oxoandrostanes , 2008, Steroids.

[5]  R. Mohareb,et al.  Synthesis of progesterone heterocyclic derivatives of potential antimicrobial activity , 2008, Acta pharmaceutica.

[6]  A. Negi,et al.  Synthesis of chalcone derivatives on steroidal framework and their anticancer activities , 2007, Steroids.

[7]  Z. Nowakowska A review of anti-infective and anti-inflammatory chalcones. , 2007, European journal of medicinal chemistry.

[8]  J. Ju,et al.  Structural requirement of chalcones for the inhibitory activity of interleukin-5. , 2007, Bioorganic & medicinal chemistry.

[9]  N. Lawrence,et al.  Effects of α-substitutions on structure and biological activity of anticancer chalcones , 2006 .

[10]  Yuan Zhang,et al.  A novel chalcone from Coreopsis tinctoria Nutt. , 2006 .

[11]  N. Davidson,et al.  Anticancer activities of novel chalcone and bis-chalcone derivatives. , 2006, Bioorganic & medicinal chemistry.

[12]  Y. Hsu,et al.  Chalcone inhibits the proliferation of human breast cancer cell by blocking cell cycle progression and inducing apoptosis. , 2006, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[13]  Sarot Cheenpracha,et al.  Anti-HIV-1 protease activity of compounds from Boesenbergia pandurata. , 2006, Bioorganic & medicinal chemistry.

[14]  R. Yunes,et al.  Synthesis of chalcone analogues with increased antileishmanial activity. , 2006, Bioorganic & medicinal chemistry.

[15]  D. Sohn,et al.  Heme oxygenase 1 mediates anti-inflammatory effects of 2',4',6'-tris(methoxymethoxy) chalcone. , 2006, European journal of pharmacology.

[16]  Takashi Suzuki,et al.  Chalcones and other compounds from the exudates of Angelica keiskei and their cancer chemopreventive effects. , 2006, Journal of natural products.

[17]  Sébastien Charneau,et al.  New syntheses and potential antimalarial activities of new 'retinoid-like chalcones'. , 2006, European journal of medicinal chemistry.

[18]  Shweta,et al.  Prenylated chalcones isolated from Crotalaria genus inhibits in vitro growth of the human malaria parasite Plasmodium falciparum. , 2005, Bioorganic & medicinal chemistry letters.

[19]  Jiri Gut,et al.  Synthesis and evaluation of new antimalarial phenylurenyl chalcone derivatives. , 2005, Journal of medicinal chemistry.

[20]  J. Vaya,et al.  Chalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers. , 2004, Phytochemistry.

[21]  R. Furlan,et al.  Antifungal chalcones and new caffeic acid esters from Zuccagnia punctata acting against soybean infecting fungi. , 2004, Journal of agricultural and food chemistry.

[22]  J. Ju,et al.  Structural requirement of isoflavonones for the inhibitory activity of interleukin-5. , 2003, European journal of medicinal chemistry.

[23]  T. Liljefors,et al.  Antileishmanial chalcones: statistical design, synthesis, and three-dimensional quantitative structure-activity relationship analysis. , 1998, Journal of medicinal chemistry.

[24]  F. R. Heerden,et al.  A Procedure for the Preparation of Cardioactive Steroid Precursors: Synthesis of 3β‐Acetoxy‐21‐hydroxy‐5α‐pregn‐14‐en‐20‐one. , 1997 .

[25]  M. Maillard,et al.  Antimicrobial steroids from the fungus Fomitopsis pinicola. , 1996, Phytochemistry.

[26]  G. Kuttan,et al.  Anticancer and antioxidant activity of synthetic chalcones and related compounds. , 1995, Cancer letters.

[27]  H. Crooks,et al.  Sterols. CXLV. 21-Benzal-5-pregnen-3(β)-ol-20-one and Allied Compounds1 , 1942 .