+++Sciencedirect: 8 статей

[Prok]

Добрый день! Помогите, пожалуйста, со статьями:

1) Acridones circumvent P-glycoprotein-associated multidrug resistance (MDR) in cancer cells
Bioorganic & Medicinal Chemistry, Volume 16, Issue 1, 1 January 2008, Pages 474-487
Vadiraj S. Gopinath, Padma Thimmaiah, Kuntebommanahalli N. Thimmaiah
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TF8-4PNM46G-4&_user=10&_coverDate=01%2F01%2F2008&_alid=840994223&_rdoc=64&_fmt=high&_orig=search&_cdi=5220&_sort=d&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=54d142bd1c46fa02ad2e2dd3f7b4723c

Код: Выделить всё

http://dx.doi.org/10.1016/j.bmc.2007.09.020

2) Acridone derivatives: Design, synthesis, and inhibition of breast cancer resistance protein ABCG2
Bioorganic & Medicinal Chemistry, Volume 15, Issue 8, 15 April 2007, Pages 2892-2897
Ahcene Boumendjel, Sira Macalou, Abdelhakim Ahmed-Belkacem, Madeleine Blanc, Attilio Di Pietro
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TF8-4N206XD-2&_user=10&_coverDate=04%2F15%2F2007&_alid=840994223&_rdoc=93&_fmt=high&_orig=search&_cdi=5220&_sort=d&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=9e46e94aee6dfe47b65f8a5f1e1c4c05

Код: Выделить всё

http://dx.doi.org/10.1016/j.bmc.2007.02.017

3) Design and synthesis of new pyranoxanthenones bearing a nitro group or an aminosubstituted side chain on the pyran ring. Evaluation of their growth inhibitory activity in breast cancer cells
European Journal of Medicinal Chemistry, Volume 42, Issue 3, March 2007, Pages 307-319
George Kolokythas, Ioannis K. Kostakis, Nicole Pouli, Panagiotis Marakos, Olga Ch. Kousidou, George N. Tzanakakis, Nikos K. Karamanos
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6VKY-4MGVHTG-2&_user=10&_coverDate=03%2F31%2F2007&_alid=840994223&_rdoc=99&_fmt=high&_orig=search&_cdi=6135&_sort=d&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=c930e746821b76c1783d98c6731675e7

Код: Выделить всё

http://dx.doi.org/10.1016/j.ejmech.2006.10.018

4)Acridone and furoquinoline alkaloids from Teclea gerrardii (Rutaceae: Toddalioideae) of southern Africa
Phytochemistry, Volume 68, Issue 5, March 2007, Pages 663-667
Alain F. Kamdem Waffo, Philip H. Coombes, Neil R. Crouch, Dulcie A. Mulholland, Sawsan M.M. El Amin, Peter J. Smith
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TH7-4MK6148-1&_user=10&_coverDate=03%2F31%2F2007&_alid=840994223&_rdoc=102&_fmt=high&_orig=search&_cdi=5275&_st=13&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=3fe2ed87ccba60432ab438be829ca223

Код: Выделить всё

http://dx.doi.org/10.1016/j.phytochem.2006.10.011

5) Chemico-enzymatic synthesis of a new fluorescent-labeled DNA by PCR with a thymidine nucleotide analogue bearing an acridone derivative
Bioorganic & Medicinal Chemistry Letters, Volume 17, Issue 3, 1 February 2007, Pages 776-779
Atsushi Shoji, Tomoya Hasegawa, Masayasu Kuwahara, Hiroaki Ozaki, Hiroaki Sawai
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TF9-4M6XMFM-7&_user=10&_coverDate=02%2F01%2F2007&_alid=840994223&_rdoc=104&_fmt=high&_orig=search&_cdi=5221&_st=13&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=dc2eafb23d0cbe27ffb18bf2608c59a8

Код: Выделить всё

http://dx.doi.org/10.1016/j.bmcl.2006.10.072

6) Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity
Bioorganic & Medicinal Chemistry, Volume 14, Issue 16, 15 August 2006, Pages 5467-5480
John R. Goodell, Avni A. Madhok, Hiroshi Hiasa, David M. Ferguson
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TF8-4K0FFSR-2&_user=10&_coverDate=08%2F15%2F2006&_alid=840994223&_rdoc=126&_fmt=high&_orig=search&_cdi=5220&_st=13&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=7030dd352db869c47f050714d8abc5b6

Код: Выделить всё

http://dx.doi.org/10.1016/j.bmc.2006.04.044

7) Alkaloids from Oriciopsis glaberrima Engl. (Rutaceae)
Phytochemistry, Volume 67, Issue 5, March 2006, Pages 475-480
Jean Duplex Wansi, Jean Wandji, Alain François Kamdem Waffo, Happi Emmanuel Ngeufa, Jean Claude Ndom, Serge Fotso, Rajendra Prasad Maskey, Dieudonné Njamen, Tanee Zacharias Fomum, Harmut Laatsch
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TH7-4HM7S34-1&_user=10&_coverDate=03%2F31%2F2006&_alid=840994223&_rdoc=136&_fmt=high&_orig=search&_cdi=5275&_st=13&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=30908a50cab9b3a6521b67e72ed39b5a

Код: Выделить всё

http://dx.doi.org/10.1016/j.phytochem.2005.09.031

Synthesis of C8-linked pyrrolo[2,1-c][1,4]benzodiazepine-acridone/acridine hybrids as potential DNA-binding agents
Bioorganic & Medicinal Chemistry Letters, Volume 14, Issue 15, 2 August 2004, Pages 4107-4111
Ahmed Kamal, O Srinivas, P Ramulu, G Ramesh, P.Praveen Kumar
абстракт:

Код: Выделить всё

http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TF9-4CPDFS6-1&_user=10&_coverDate=08%2F02%2F2004&_alid=840994223&_rdoc=193&_fmt=high&_orig=search&_cdi=5221&_st=13&_docanchor=&view=c&_ct=828&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=5b6d233bc5ce9d6945d4fa576ecd111d

Код: Выделить всё

http://dx.doi.org/10.1016/j.bmcl.2004.04.087

[vladbond]

ii

[vladbond]

yy

[vladbond]

uu

[Prok]

Огромное спасибо, vladbond!