| [1] Poirier D,Chang H J,Azzi A,et al. Estrone and Estradiol C-16 Derivatives as Inhibitors of Type 1 17β-Hydroxysteroid Dehydrogenase[J]. Mol Cell Endocrinol,2006,248(1/2):236-238.[2] Banday A H,Zargar M I,Ganaie B A. Synthesis and Antimicrobial Studies of Chalconyl Pregnenolones[J]. Steroids,2011,76(12):1358-1362.[3] Kakati D,Sarma R K,Saikia R,et al. Rapid Microwave Assisted Synthesis and Antimicrobial Bioevaluation of Novel Steroidal Chalcones[J]. Steroids,2013,78(3):321-326.[4] Chattopadhaya R,Jindal D P,Minu M,et al. Synthesis and Cytotoxic Studies of Hydroximino Derivatives of Some 16-E-Arylidenosteroids[J]. Arzneim-Forsch/Drug Res,2004,54(9):456-466.[5] Dubey S,Piplani P,Jindal D P. Synthesis and In Vitro Antineoplastic Evaluation of Certain 16-(4-Substituted Benzylidene) Derivatives of Androst-5-ene[J]. Chem Biodivers,2004,1(10):1529-1536.[6] Shan L H,Liu H M,Huang K X,et al. Synthesis of 3β,7α,11α-Trihydroxy-pregn-21-benzylidene-5-en-20-one Derivatives and Their Cytotoxic Activities[J]. Bioorg Med Chem Lett,2009,19(23):6637-6639.[7] Khuri N,Usubillaga A,Vaz S C,et al. Synthesis, Stereochemical Analysis, and Neuromuscular Blocking Activity of Oximino Ether Derivatives of Progesterone[J]. J Pharm Sci,1991,80(7):661-664.[8] Abdelhamid A O,Mervat M A,Gamal A E. New Routes to Steroidal Heterocyclic Derivatives: Synthesis of Biologically Active Pyrazolyl- and Isoxazolylpregnene Derivatives[J]. J Heterocycl Chem,2007,44(1):7-11.[9] MacNevin C J,Atif F,Sayeed I,et al. Development and Screening of Water-soluble Analogues of Progesterone and Allopregnanolone in Models of Brain Injury[J]. J Med Chem,2009,52(19):6012-6023.[10] Mohareb R M,Elmegeed G A,Baiuomy A R,et al. Evaluation of Anti-inflammatory, Anti-nociceptive, and Anti-ulcerogenic Activities of Novel Synthesized Thiazolyl and Pyrrolyl Steroids[J]. Arch Pharm Chem Life Sci,2011,344(10):595-604.[11] Jin C S,Roh J S,Sun W S,et al. N-Benzylbenzamides:A New Class of Potent Tyrosinase Inhibitors[J]. Bioorg Med Chem Lett,2006,16(10):2682-2684.[12] Ren J,Wang Y C,Wang J L,et al. Synthesis and Antitumor Activity of N-Sulfonyl-3,7-dioxo-5β-cholan-24-amides, Ursodeoxycholic Acid Derivatives[J]. Steroids,2013,78(1):53-58.[13] Khan K M,Saeed S,Ali M,et al. Unsymmetrically Disubstituted Urea Derivatives:a Potent Class of Antiglycating Agents[J]. Bioorg Med Chem,2009,17(15):2447-2451.[14] Fan N J,Bai Y B,Zhang F Y,et al. Synthesis and Cytotoxicity Of Some Novel 21E-Benzylidene Steroidal Derivatives[J]. Steroids,2013,78(9):874-879.[15] Ono M,Haratake M,Mori H,et al. Novel Chalcones as Probes for In Vivo Imaging of β-Amyloidplaques in Alzheimer′s Brains[J]. Bioorg Med Chem,2007,15(21):6802-6809.[16] Sonmez F,Sevmezler S,Atahan A,et al. Evaluation of New Chalcone Derivatives as Polyphenol Oxidase Inhibitors[J]. Bioorg Med Chem Lett,2011,21(24):7479-7482.[17] VanVliet D S,Gillespie P,Scicinski J J. Rapid One-pot Preparation of 2-Substituted Benzimidazoles from 2-Nitroanilines Using Microwave Conditions[J]. Tetrahedron Lett,2005,46(39):6741-6743. |
