Design and synthesis of benzo [c, d] indolone-pyrrolobenzodiazepine conjugates as potential anticancer agents

…, M Vishnuvardhan, S Ramakrishna, G Srinivas

Index: Kamal, Ahmed; Ramakrishna; Lakshma Nayak; Raju; Subba Rao; Viswanath; Vishnuvardhan; Ramakrishna, Sistla; Srinivas Bioorganic and Medicinal Chemistry, 2012 , vol. 20, # 2 p. 789 - 800

Full Text: HTML

Citation Number: 23

Abstract

A series of benzo [c, d] indol-2 (1H) one-PBD conjugates (11a–l) have been designed and synthesized as potential anticancer agents. These compounds were prepared by linking the C8-position of DC-81 with a benzo [c, d] indol-2 (1H) one moiety through different alkane spacers in good yields and confirmed by 1H NMR, mass and HRMS data. The DNA binding ability of these conjugates was evaluated by thermal denaturation studies and ...

Related Articles:

Selective Synthesis of m eso-Naphthylporphyrins

[Cammidge, Andrew N.; Oeztuerk, Orhan Journal of Organic Chemistry, 2002 , vol. 67, # 21 p. 7457 - 7464]

Studies on the Lossen-type rearrangement of N-(3-phenylpropionyloxy) phthalimide and N-tosyloxy derivatives with several nucleophiles

[Tetrahedron, , vol. 66, # 12 p. 2132 - 2140]

Studies on the Lossen-type rearrangement of N-(3-phenylpropionyloxy) phthalimide and N-tosyloxy derivatives with several nucleophiles

[Tetrahedron, , vol. 66, # 12 p. 2132 - 2140]

Antioxidant Activity of New Benzo [de] quinolines and Lactams: 2DQuantitative Structure-Activity Relationships

[Medicinal Chemistry, , vol. 8, # 5 p. 942 - 946]

Aristoxazole analogues. Conversion of 8-nitro-1-naphthoic acid to 2-methylnaphtho [1, 2-d] oxazole-9-carboxylic acid: Comments on the chemical mechanism of …

[Journal of Natural Products, , vol. 75, # 7 p. 1414 - 1418]

More Articles...