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Items: 1 to 20 of 122

1.

Diversity-oriented synthesis of α-aminophosphonates: a new class of potential anticancer agents.

Bhattacharya AK, Raut DS, Rana KC, Polanki IK, Khan MS, Iram S.

Eur J Med Chem. 2013 Aug;66:146-52. doi: 10.1016/j.ejmech.2013.05.036.

PMID:
23792352
2.

Green synthesis of α-aminophosphonate derivatives on a solid supported TiO2 -SiO2 catalyst and their anticancer activity.

Chinthaparthi RR, Bhatnagar I, Gangireddy CS, Syama SC, Cirandur SR.

Arch Pharm (Weinheim). 2013 Sep;346(9):667-76. doi: 10.1002/ardp.201300214.

PMID:
23959690
3.

Synthesis and antitumor activity of α-aminophosphonates containing thiazole[5,4-b]pyridine moiety.

Gu L, Jin C.

Org Biomol Chem. 2012 Sep 21;10(35):7098-102. doi: 10.1039/c2ob25875g.

PMID:
22850968
4.

Synthesis and antitumor activities of novel α-aminophosphonates dehydroabietic acid derivatives.

Huang XC, Wang M, Pan YM, Tian XY, Wang HS, Zhang Y.

Bioorg Med Chem Lett. 2013 Oct 1;23(19):5283-9. doi: 10.1016/j.bmcl.2013.08.005.

PMID:
23988357
5.

Synthesis and antiproliferative activity of novel α-aminophosphonates.

Mungara AK, Park YK, Lee KD.

Chem Pharm Bull (Tokyo). 2012;60(12):1531-7.

6.

Synthesis and antitumor activities of novel thiourea α-aminophosphonates from dehydroabietic acid.

Huang XC, Wang M, Pan YM, Yao GY, Wang HS, Tian XY, Qin JK, Zhang Y.

Eur J Med Chem. 2013 Nov;69:508-20. doi: 10.1016/j.ejmech.2013.08.055.

PMID:
24095745
7.

PEG-SO(3)H catalyzed synthesis and cytotoxicity of α-aminophosphonates.

Reddy CB, Kumar KS, Kumar MA, Narayana Reddy MV, Krishna BS, Naveen M, Arunasree MK, Reddy CS, Raju CN, Reddy CD.

Eur J Med Chem. 2012 Jan;47(1):553-9. doi: 10.1016/j.ejmech.2011.11.026.

PMID:
22136905
8.

Design and one-pot synthesis of alpha-aminophosphonates and bis(alpha-aminophosphonates) by iron(III) chloride and cytotoxic activity.

Rezaei Z, Firouzabadi H, Iranpoor N, Ghaderi A, Jafari MR, Jafari AA, Zare HR.

Eur J Med Chem. 2009 Nov;44(11):4266-75. doi: 10.1016/j.ejmech.2009.07.009.

PMID:
19679380
9.

Green synthesis and biological evaluation of new di-α-aminophosphonate derivatives as cytotoxic agents.

Uma Maheswara Rao K, Namkoong S, Yu HC, Park J, Chung CM, Oh SY.

Arch Pharm (Weinheim). 2013 Dec;346(12):851-9. doi: 10.1002/ardp.201300249.

PMID:
24214666
10.

Synthesis and antitumor activities of novel rhein α-aminophosphonates conjugates.

Yao GY, Ye MY, Huang RZ, Li YJ, Pan YM, Xu Q, Liao ZX, Wang HS.

Bioorg Med Chem Lett. 2014 Jan 15;24(2):501-7. doi: 10.1016/j.bmcl.2013.12.030.

PMID:
24378217
11.

Synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates and their anticancer properties.

Kalla RM, Choi JS, Yoo JW, Byeon SJ, Heo MS, Kim I.

Eur J Med Chem. 2014 Apr 9;76:61-6. doi: 10.1016/j.ejmech.2014.02.025.

PMID:
24568757
12.

Carbodiimides in the synthesis of enamino- and α-aminophosphonates as peptidomimetics of analgesic/antiinflammatory and anticancer agents.

Abdou WM, Barghash RF, Bekheit MS.

Arch Pharm (Weinheim). 2012 Nov;345(11):884-95. doi: 10.1002/ardp.201200142.

PMID:
22930562
13.

Synthesis and biological characterization of new aminophosphonates for mitochondrial pH determination by (31)P NMR spectroscopy.

Culcasi M, Casano G, Lucchesi C, Mercier A, Clément JL, Pique V, Michelet L, Krieger-Liszkay A, Robin M, Pietri S.

J Med Chem. 2013 Mar 28;56(6):2487-99. doi: 10.1021/jm301866e.

PMID:
23437893
14.

Novel Coumarin-Containing Aminophosphonatesas Antitumor Agent: Synthesis, Cytotoxicity, DNA-Binding and Apoptosis Evaluation.

Li YJ, Wang CY, Ye MY, Yao GY, Wang HS.

Molecules. 2015 Aug 13;20(8):14791-809. doi: 10.3390/molecules200814791.

15.

Design and synthesis of pyrimidine molecules endowed with thiazolidin-4-one as new anticancer agents.

Rashid M, Husain A, Shaharyar M, Mishra R, Hussain A, Afzal O.

Eur J Med Chem. 2014 Aug 18;83:630-45. doi: 10.1016/j.ejmech.2014.06.033.

PMID:
25010935
16.

Design, synthesis, antioxidant, and anti-breast cancer activities of novel diethyl(alkyl/aryl/heteroarylamino)(4-(pyridin-2-yl)phenyl)methylphosphonates.

Prasad SS, Kumar KS, Jayaprakash SH, Krishna BS, Sundar CS, Rao PV, Babu TM, Rajendra W, Reddy CS.

Arch Pharm (Weinheim). 2013 May;346(5):380-91. doi: 10.1002/ardp.201300032.

PMID:
23589377
17.

Synthesis, NMR characterization and in vitro antitumor evaluation of new aminophosphonic acid diesters.

Kraicheva I, Bogomilova A, Tsacheva I, Momekov G, Troev K.

Eur J Med Chem. 2009 Aug;44(8):3363-7. doi: 10.1016/j.ejmech.2009.03.017.

PMID:
19361895
18.

QSAR modeling, synthesis and bioassay of diverse leukemia RPMI-8226 cell line active agents.

Katritzky AR, Girgis AS, Slavov S, Tala SR, Stoyanova-Slavova I.

Eur J Med Chem. 2010 Nov;45(11):5183-99. doi: 10.1016/j.ejmech.2010.08.033.

PMID:
20843586
19.

Synthesis of new class of spirocarbocycle derivatives by multicomponent domino reaction and their evaluation for antimicrobial, anticancer activity and molecular docking studies.

Sudhapriya N, Perumal PT, Balachandran C, Ignacimuthu S, Sangeetha M, Doble M.

Eur J Med Chem. 2014 Aug 18;83:190-207. doi: 10.1016/j.ejmech.2014.05.065.

PMID:
24956555
20.

Novel carbapenem chalcone derivatives: synthesis, cytotoxicity and molecular docking studies.

Kommidi DR, Pagadala R, Rana S, Singh P, Shintre SA, Koorbanally NA, Jonnalagadda SB, Moodley B.

Org Biomol Chem. 2015 Apr 14;13(14):4344-50. doi: 10.1039/c5ob00197h.

PMID:
25767041
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