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One-Pot Access to Indolo[2,3-b]quinolines by Electrophile-Triggered Cross-Amination/Friedel-Crafts Alkylation of Indoles with 1-(2-Tosylaminophenyl)ketonesALI, Shaukat; LI, Ying-Xiu; ANWAR, Saeed et al.Journal of organic chemistry. 2012, Vol 77, Num 1, pp 424-431, issn 0022-3263, 8 p.Article

A Concise Synthesis of 6H-Indolo[2,3-b]quinolines: Formal Synthesis of NeocryptolepineKADAM, Hari K; PARVATKAR, Prakash T; TILVE, Santosh G et al.Synthesis (Stuttgart). 2012, Num 9, pp 1339-1342, issn 0039-7881, 4 p.Article

New derivatives of 11-methyl-6-[2-(dimethylamino)ethyl]-6H-indolo[2,3-b]quinoline as cytotoxic DNA topoisomerase II inhibitorsLUNIEWSKI, Wojciech; WIETRZYK, Joanna; GODLEWSKA, Joanna et al.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 19, pp 6103-6107, issn 0960-894X, 5 p.Article

Indoloquinolines as Scaffolds for Drug DiscoveryLAVRADO, J; MOREIRA, R; PAULO, A et al.Current medicinal chemistry. 2010, Vol 17, Num 22, pp 2348-2370, issn 0929-8673, 23 p.Article

Isoneocryptolepine, a synthetic indoloquinoline alkaloid, as an antiplasmodial lead compoundVAN MIERT, Sabine; HOSTYN, Steven; PIETERS, Luc et al.Journal of natural products (Print). 2005, Vol 68, Num 5, pp 674-677, issn 0163-3864, 4 p.Article

In vitro and in vivo antiplasmodial activity of cryptolepine and related alkaloids from Cryptolepis sanguinolentaCIMANGA, K; DE BRUYNE, T; PIETERS, L et al.Journal of natural products (Print). 1997, Vol 60, Num 7, pp 688-691, issn 0163-3864Article

Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; structure―activity relationships of neocryptolepines and 6-methyl congenersLI WANG; SWITALSKA, Marta; MEI, Zhen-Wu et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 15, pp 4820-4829, issn 0968-0896, 10 p.Article

Microwave-Assisted Syntheses of N-Heterocycles Using Alkenone-, Alkynone-and Aryl-carbonyl O-Phenyl Oximes : Formal Synthesis of NeocryptolepinePONELA-CUBILLO, Fernando; SCOTT, Jackie S; WALTON, John C et al.Journal of organic chemistry. 2008, Vol 73, Num 14, pp 5558-5565, issn 0022-3263, 8 p.Article

Highly efficient one-pot synthesis of D-ring chloro-substituted neocryptolepines via a condensation—Pd—catalyzed intramolecular direct arylation strategyHOSTYN, Steven; KOUROSCH ABBASPOUR TEHRANI; LEMIERE, Filip et al.Tetrahedron (Oxford. Print). 2011, Vol 67, Num 3, issn 0040-4020, 566, 655-659 [6 p.]Article

Synthesis, cytotoxicity, and antiplasmodial and antitrypanosomal activity of new neocryptolepine derivativesJONCKERS, Tim H. M; VAN MIERT, Sabine; ROZENSKI, Jef et al.Journal of medicinal chemistry (Print). 2002, Vol 45, Num 16, pp 3497-3508, issn 0022-2623Article

Synthesis and Antiplasmodial Activity of Aminoalkylamino-Substituted Neocryptolepine DerivativesEL SAYED, Ibrahim; VAN DER VEKEN, Pieter; JOOSSENS, Jurgen et al.Journal of medicinal chemistry (Print). 2009, Vol 52, Num 9, pp 2979-2988, issn 0022-2623, 10 p.Article

DNA intercalation, topoisomerase II inhibition and cytotoxic activity of the plant alkaloid neocryptolepineBAILLY, Christian; LAINE, William; BALDEYROU, Brigitte et al.Anti-cancer drug design. 2000, Vol 15, Num 3, pp 191-201, issn 0266-9536Article