+++Статьи из ACS_Pub

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Доброго дня, коллеги! Помогите пожалуйста со статьями:
1)
Incorporation of Basic Side Chains into Cryptolepine Scaffold: Structure−Antimalarial Activity Relationships and Mechanistic Studies
Joao Lavrado, Ghislain G. Cabal, Miguel Prudencio, Maria M. Mota, Jiri Gut, Philip J. Rosenthal, Cecilia Diaz, Rita C. Guedes, Daniel J. V. A. dos Santos, Elena Bichenkova, Kenneth T. Douglas, Rui Moreira, and Alexandra Paulo
J. Med. Chem., 2011, 54 (3), pp 734–750

DOI:

http://dx.doi.org/10.1021/jm101383f

2)
Synthesis and Biological Evaluation of Analogues of Cryptolepine, an Alkaloid Isolated from the Suriname Rainforest1
Shu-Wei Yang, Maged Abdel-Kader, Stan Malone, Marga C. M. Werkhoven, Jan H. Wisse, Isia Bursuker, Kim Neddermann, Craig Fairchild, Carmen Raventos-Suarez, Ana T. Menendez, Kate Lane, and David G. I. Kingston
J. Nat. Prod., 1999, 62 (7), pp 976–983

DOI:

http://dx.doi.org/10.1021/np990035g

3)
Synthesis of Some Cryptolepine Analogues, Assessment of Their Antimalarial and Cytotoxic Activities, and Consideration of Their Antimalarial Mode of Action
Onyeka Onyeibor, Simon L. Croft, Hilary I. Dodson, Mohammad Feiz-Haddad, Howard Kendrick, Nicola J. Millington, Silvia Parapini, Roger M. Phillips, Scott Seville, Steven D. Shnyder, Donatella Taramelli, and Colin W. Wright
J. Med. Chem., 2005, 48 (7), pp 2701–2709

DOI:

http://dx.doi.org/10.1021/jm040893w

4)
Synthesis and Evaluation of Cryptolepine Analogues for Their Potential as New Antimalarial Agents
Colin W. Wright, Jonathan Addae-Kyereme, Anthony G. Breen, John E. Brown, Marlene F. Cox, Simon L. Croft, Yaman Gökçek, Howard Kendrick, Roger M. Phillips, and Pamela L. Pollet
J. Med. Chem., 2001, 44 (19), pp 3187–3194

DOI:

http://dx.doi.org/10.1021/jm010929+

5)
Synthesis, Cytotoxicity, and Antiplasmodial and Antitrypanosomal Activity of New Neocryptolepine Derivatives
Tim H. M. Jonckers, Sabine van Miert, Kanyanga Cimanga, Christian Bailly, Pierre Colson, Marie-Claire De Pauw-Gillet, Hilde van den Heuvel, Magda Claeys, Filip Lemière, Eddy L. Esmans, Jef Rozenski, Ludo Quirijnen, Louis Maes, Roger Dommisse, Guy L. F. Lemière, Arnold Vlietinck, and Luc Pieters
J. Med. Chem., 2002, 45 (16), pp 3497–3508

DOI:

http://dx.doi.org/10.1021/jm011102i

6)
An Expeditious I2-Catalyzed Entry into 6H-Indolo[2,3-b]quinoline System of Cryptotackieine
Prakash T. Parvatkar, Perunninakulath S. Parameswaran and Santosh G. Tilve
J. Org. Chem., 2009, 74 (21), pp 8369–8372

DOI:

http://dx.doi.org/10.1021/jo901361x

7)
Ibrahim El Sayed, Pieter Van der Veken, Koen Steert, Liene Dhooghe, Steven Hostyn, Gitte Van Baelen, Guy Lemiere, Bert U. W. Maes, Paul Cos, Louis Maes, Jurgen Joossens, Achiel Haemers, Luc Pieters and Koen Augustyns
J. Med. Chem., 2009, 52 (9), pp 2979–2988

DOI:

http://dx.doi.org/10.1021/jm801490z

8)
Efficient Syntheses of the Unknown Quinolino[2,3-c]cinnolines; Synthesis of Neocryptolepines
Makhluf J. Haddadin, Raghida M. Bou Zerdan, Mark J. Kurth, and James C. Fettinger
Org. Lett., 2010, 12 (23), pp 5502–5505

DOI:

http://dx.doi.org/10.1021/ol102376a

Большое спасибо!

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ЗдОрово, спасибо!