参考文献/References:
[1] VARKI A.CUMMINGS D C,ESKO J D,et al.Essentials of glycobiology[M].2nd ed.New York:Cold Spring Harbor Laboratory Press,2009:47-61.
[2] TEWARI N,TIWARIV K,MISHRA R C,et al.Synthesis and bioevaluation of glycosyl ureas as α-glucosidase inhibitors and their effect on mycobacterium[J].Bioorganic & Medicinal Chemistry,2003,11(13):2911-2922.
[3] VELAZQUFZ S,CHAMORRO C,PEREZ M J,et al.Abasic analogues of TSAO-T as the first sugar derivatives that specifically inhibit HIV-1 reverse transcriptase[J].Journal of Medicinal Chemistry,1998,41(23):4636-4647.
[4] MCALINDON T E,LAVALLEY M P,GULIN J P,et al.Glucosa mine and ehondroitin for treatment of osteoarthritis: Asystematic quality assessment and met-analysis[J].The Journal of the American Medical Association,2000,283(11):1469-1475.
[5] QUASTEL J H.Inhibition of tumour growth by D-glucosa mine[J].Nature,1953,171(4345):252-254.
[6] BEKIES J TELG,WINZLER R J.Inhibitory effects of D-glucosa mine on the growth of Walker 256 carcinosarcoma and on protein, RNA, and DNA synthesis[J].Cancer Research,1970,30(12):2905-2912.
[7] 罗宣干,卓仁禧.5-氟脲嘧啶的D-氨基葡萄糖衍生物的合成及其抗肿瘤活性研究[J].高等学校化学学报,1996,17(9):1416-1420.
[8] RITTER T K,WONG C H.Synthesis of N-acetylglucosa mine thiazoline/lipid II hybrids[J].Tetrahedron Letters,2001,42(4):615-618.
[9] TOURNAIRE-ARELLANO C,YOUNES-El HAGE S,VALESP,et al.Synthesis and biological evaluation of ureido and thioureido derivatives of 2-a mino-2-deoxy-D-glucose and related a minoalcohols as N-acetyl-β-D-hexosa minidase inhibitors[J].Carbohydrate Research,1998,314(1):47-63.
[10] CHAUDHARY P,KUMAR R,VERMA A K,et al.Synthesis and antimicrobial activity of N-alkyl and N-aryl piperazine derivatives[J].Bioorganic & Medicinal Chemistry,2006,14(6):1819-1826.
[11] DOUD,HE G,MANDADAPU S R,et al.Inhibition of noroviruses by piperazine derivatives[J].Bioorganic & Medicinal Chemistry Letters,2012,22(1):377-379.
[12] CAO Sheng-li,HAN Ye,YUAN Chang-zheng,et al.Synthesis and antiproliferative activity of 4-substituteD-piperazine-1-carbodithioate derivatives of 2,4-dia minoquinazoline[J].European Journal of Medicinal Chemistry,2013,64:401-409.
[13] CHEN K X,LI Z G,XIE H Y,et al.Quantitative structure-activity relationship analysis of aryl alkanol piperazine derivatives with antidepressant activities[J].European Journal of Medicinal Chemistry,2009,44(11):4367-4375.
[14] FOROUMADI A,EMAMI S,MEHNI M,et al.Synthesis and antibacterial activity of N-[2-(5-bromothiophen-2-yl)-2-oxoethyl] and N-[(2-5-bromothiophen-2-yl)-2-oxi minoethyl] derivatives of piperazinyl quinolones[J].Bioorganic and Medicinal Chemistry Letters,2005,15(20):4536-4539.
[15] PACCHIANO F,CRTA F,MCDONALD P C,et al.Ureido-substituted benzenesulfonam-ides potently inhibit carbonic anhydrase IX and show antimetastatic activity in a model of breast cancer metastasis[J].Journal of Medicinal Chemistry,2011,54(6):1896-1902.
[16] 尹学琼,黄建,于长江,等.D-氨基葡萄糖Schiff碱的制备及抑制真菌性能研究[J].化学试剂,2010,32(11),961-964
[17] 刘玮炜,吴杨全,龚峰,等.N-硝基苯甲酰基-1,3,4,6-四-O-乙酰基-2-脱氧-β-D-氨基葡萄 糖的合成与表征[J].华侨大学学报:自然科学版,2013,34(1):56-58.